NZ624449B2

NZ624449B2 - Antiseptic cap equipped syringe

Info

Publication number: NZ624449B2
Application number: NZ624449A
Authority: NZ
Inventors: William Anderson; Larry Colquitt; Christopher E Gardner; Gary Henniger; Chirag Sanjay Walawalkar; Mark Wilson
Original assignee: Excelsior Medical Corporation
Priority date: 2011-11-03
Filing date: 2012-10-26
Publication date: 2016-09-27

Abstract

syringe assembly including: a barrel defining a chamber; a plunger mounted in the chamber and moveable with respect to the barrel (1240); and a cap holder assembly (1220) containing a cap and an absorbent material removably attached to the syringe. The antiseptic cap can be removed by pushing the base of the cap via apertures in the chamber (1270). base of the cap via apertures in the chamber (1270).

Description

/062078 ANTISEPTIC CAP ED SYRINGE CROSS—REFERENCE TO RELATED ATION This application claims the beneﬁt of the priority of US. Application Serial No. 13/547,650, ﬁled on July 12, 2012, which is a continuation—in—part of US. Application Serial No. 13/288,529, ﬁled on November 3, 2011, which is a continuation-in-part of US.

Application Serial No. 12/214,526, ﬁled on June 19, 2008, which is a continuation-in-part of US. Application Serial No. 11/821,190 ﬁled on June 22, 2007, now US. Patent No. 8,167,847, which claims the beneﬁt of US. Provisional Application Serial No. 60/815,806 ﬁled on June 22, 2006, and US. Patent Application Serial No. 13/288,529 is a continuation-in-part of US. Application Serial No. 11/821,190 ﬁled on June 22, 2007, now US. Patent No. 8,167,847, which claims the beneﬁt of US. Provisional Application Serial No. 60/815,806 ﬁled on June 22, 2006, the entire disclosures of which are all expressly incorporated herein by reference.

BACKGROUND OF THE INVENTION Technical Field The present ion relates to an antiseptic cap equipped syringe, and more speciﬁcally to antiseptic caps disposed on syringes. ound Art Catheters are widely used to treat patients requiring a variety of medical procedures.

Catheters can either be acute, or temporary, for short-term use or chronic for long-term treatment. Catheters are ly inserted into central veins (such as the vena cava) from peripheral vein sites to provide access to a patient's vascular system. ers offer many advantages for patients; for example, chronic catheters provide ready access without repeated punctures or repeated vessel cannulation for administration of large volumes of ﬂuids, nutrients and medications and for awal of blood on an intermittent basis.

With respect to the use of catheters for infusion of ﬂuids, examples include the infusion of drugs, olytes or ﬂuids used in chemotherapy. In chemotherapy, catheters are used for infusion of drugs on an ittent basis, ranging from daily to weekly.

Another example es the use of catheters in hyperalimentation treatment, wherein the catheters usually used for infusion of large volumes of ﬂuids.

For hemodialysis, catheters are commonly used-—usually three times per week——for aspiration of blood for dialysis treatment and rapid return of the blood to ation after treatment. Although a preferred mode of vascular access for a hemodialysis patient involves using an arteriovenous (AV) ﬁstula of either the upper or lower extremities or an arteriovenous “bridge” graft (typically utilizing PTFE), use of these access devices is not always possible or ble. When either of these modes of vascular access is not ble, for example, due to a paucity of adequate blood s for creation of AV “shunts” or due to nonoptimally functioning established AV shunts, a large bore venous line catheter is typically ed for hemodialysis. Catheters used for hemodialysis usually include two relatively large diameter lumens (usually molded as one catheter) for aspiration and rapid return of blood required during the hemodialysis procedure. One lumen of such a catheter is used for aspiration, or removal, of blood, while the other lumen is used for ing the blood to the patient's bloodstream.

Catheter connections, such as, for example, connections of catheters to is machine tubing, to IV line tubing, to infusion ports and to catheter caps, which are used to seal the end of a catheter to t the ity of the catheter and prevent ﬂuid loss and/or particle contamination, are most often made utilizing the medical industry's standardized Luer taper ﬁttings. These ﬁttings, which may either be male couplings or female couplings, include a tapered end of standardized dimensions. Coupling is made by the press-ﬁt of mating parts. A threaded lock—ﬁt or other type of securing mechanism is commonly utilized to ensure the integrity of the pressure ﬁt of the Luer s.

Catheters, especially chronic venous catheters, provide challenges in their use. One such challenge is that such catheters can become occluded by a thrombus. In order to prevent clotting of catheters in blood vessels between uses, such as, for example, between is ents when the catheter is essentially nonﬁinctioning and dwells inside a “central” vein (i.e. superior vena cava, inferior vena cava, iliac, etc.), the lumens of the catheter are oﬁen ﬁlled with a lock solution of a concentrated solution of the ly used anticoagulant, heparin (up to 10,000 units of heparin per er lumen).

As used herein, the terms “lock solution” or “locking solution” refer to a solution that is injected or otherwise infused into a lumen of a catheter with the intention of ng a substantial portion of the lock solution to remain in the lumen and not in the systemic blood circulation until it is desired or required to access that particular lumen again, lly for additional treatment, i.e., infusion or withdrawal of ﬂuid. In addition, attention has been given to the development of alternative lock ons with the goal of improving the patency rates of vascular catheters. For example, lower-alcohol containing locking solutions are under development wherein the lower alcohols include ethanol, propanol and butanol. Anti-microbial and or anticoagulant additives can optionally be added to the lower-alcohol ning locking solution. Preferably the lock solution can remain in the lumen for a desired amount of time lasting from about 1 hour to 3 or 4 days or longer.

For the reasons set forth above, signiﬁcant care must be taken when infusing medications, nutrients and the like into a catheter, and when “looking” a catheter between uses, to ze the risks associated with an indwelling catheter, including the risk of thrombosis or clotting, the risk of excessive anticoagulating and the risk of infection.

Syringes are lly used to ster the required amount of catheter lock solution (determined by the catheter manufacturer) into an indwelling catheter after a given use.

Flush ures also require that care be taken to prevent blood reﬂux into the catheter.

Reﬂux in I.V. therapy is the term commonly used to describe the ﬂuid that is drawn back into the catheter after a ﬂush ure. The concern is that the reﬂux ﬂuid contains blood or solution that could cause the catheter to occlude. To ensure that reﬂux does not occur, ﬂush procedures t two techniques: 1) at the end of the ﬂush solution delivery, the user maintains pressure on the syringe plunger while clamping the I.V. line; or 2) while delivering the last 0.5 ml of ﬂush solution disconnect the syringe from the I.V. port or clamp the IV. line. Either technique maintains positive pressure on the ﬂuid in the er to prevent reﬂux of ﬂuid and blood.

It has been found that the use of antiseptic caps, such as the cap manufactured and sold by Excelsior under the trademark SwabCap, greatly reduce the incidence of ions, resulting in, among other things, signiﬁcant health beneﬁts for patients and vast cost savings.

In light of the above-described problems, there is a continuing need for advancements in catheter lock techniques, devices and ures to improve the safety and efﬁcacy of catheter locking procedures and of l patient care.

SUMMARY OF THE INVENTION The present invention s to an antiseptic cap and syringe combination. The combination includes a syringe barrel having an access point connection, and a tip cap having a proximal chamber and a distal chamber. The proximal chamber releasably receives and engages the access point connection of the syringe. The distal chamber removably receives and engages an antiseptic cap. In one embodiment, the distal chamber has a plurality of ribs for coacting with a plurality of ribs on the antiseptic cap to prevent ve rotational movement between the distal chamber and the antiseptic cap.

In one embodiment, a combination syringe tip cap and antiseptic cap includes a ﬁrst chamber having means for ably ng an access point connection on a syringe. A second chamber is formed ally with the ﬁrst chamber. An ptic cap is positioned within the second chamber, and means for releasably engaging the antiseptic cap is provided in the second chamber.

A method of storing an antiseptic cap of a syringe is provided. The method includes the steps of providing a syringe having a barrel, a plunger, an access point connection and a tip cap, providing a chamber on the syringe, and ably engaging an antiseptic cap within the chamber.

A method of using an antiseptic cap disposed on a tip cap of a syringe having a , a plunger, an access point connection and a tip cap is also provided. The method includes the steps of removing the tip cap from the syringe, and using the syringe. The method further includes the step of removing a cover over the antiseptic cap. Steps of using a tip cap to position the antiseptic cap on an access point, and removing the tip cap from engagement with the antiseptic cap, leaving the antiseptic cap on the access point are included.

In one embodiment, a combination e tip cap and antiseptic cap es a ﬁrst chamber having means for releasably engaging an access point connection on a syringe, and a second chamber formed integrally with the ﬁrst chamber. An antiseptic cap assembly has an antiseptic cap, and the antiseptic cap assembly is bly positioned within the second chamber.

In another embodiment, an antiseptic cap and syringe combination includes a syringe barrel having an access point connection, and a plunger received at one end by the . The plunger has a r removeably ing an antiseptic cap assembly at a second end. A tip cap has a proximal chamber for ably receiving the access point connection of the syringe, and a distal chamber for removeably receiving a second antiseptic cap assembly.

In another ment, an antiseptic cap and syringe combination includes a e barrel having an access point connection, and a plunger ed at one end by the barrel. A chamber is interconnected with the syringe barrel for removeably receiving an antiseptic cap assembly.

In another embodiment, an ptic cap and syringe combination includes a syringe barrel having an access point connection and an antiseptic cap. A ﬂexible ring for engaging the access point, and a chamber interconnected with the e barrel for removeably receiving an antiseptic cap are provided.

In another embodiment, an ptic cap and syringe combination includes a syringe barrel having an access point connection and a tip cap including a proximal chamber releasably receiving and engaging the access point connection of the syringe. A distal projection extends from the tip cap, and an antiseptic cap assembly has a chamber for receiving the distal projection of the tip cap at one end and an antiseptic cap at the other end.

In another embodiment, an antiseptic cap and syringe combination includes a syringe barrel having an access point connection, a tip cap including a al chamber for engaging the access point connection and a distal attachment chamber, and a cap assembly. The cap assembly includes an engagement protrusion for removeably engaging the tip cap. 2012/062078 BRIEF DESCRIPTION OF THE DRAWINGS is a perspective view of an antiseptic cap equipped plunger and syringe barrel assembly prior to connection of a syringe tip to an access point to a central venous catheter; is a perspective view of an ptic cap equipped r and syringe barrel assembly with the syringe tip connected to an access point to a central venous catheter; is a ctive view of an antiseptic cap equipped plunger and syringe barrel assembly prior to connection of the antiseptic cap to an access point to a central venous catheter; is a perspective View of an antiseptic cap equipped plunger and syringe barrel assembly aﬁer connection of the ptic cap to an access point to a central venous catheter; is a perspective View assembly drawing of an antiseptic cap equipped plunger; is a perspective view of an antiseptic cap equipped plunger in a partially assembled state; is a perspective View of the antiseptic cap ed plunger of with a top seal; is a perspective View of an antiseptic cap equipped plunger of mounted in a lumen of a syringe barrel; is a side View in cutaway of an antiseptic cap equipped plunger and syringe barrel assembly; shows an exploded View of a detail of of one embodiment of the antiseptic cap equipped plunger and syringe barrel assembly; shows an exploded view of a detail of of r embodiment of the antiseptic cap equipped plunger and syringe barrel assembly; FIGS. 12-14 show various embodiments of grips of the antiseptic cap equipped plunger assembly; FIGS. 15-17 show various views of one embodiment antiseptic cap equipped plunger and syringe barrel ly with a barrel lock to resist rotation of the r assembly with respect to the syringe barrel; shows another embodiment of a barrel lock to resist rotation of the plunger assembly with respect to the syringe barrel; FIGS. 19-20 show various views of another embodiment antiseptic cap equipped plunger and anti—reﬂux syringe barrel assembly with a barrel lock to resist rotation of the plunger assembly with t to the syringe barrel; shows a perspective View of another ment antiseptic cap ed plunger and syringe barrel ly with a barrel lock to resist rotation of the plunger assembly with respect to the syringe barrel; FIGS. 22a,b are respectively a perspective view of an antiseptic cap without a sponge and with a sponge; FIGS. 23 and 24 are different embodiments of the antiseptic cap with varying ng es; is a perspective View of the antiseptic cap of b prior to docking with a valve; is a perspective view of the antiseptic cap of b docked with a valve; is a side View in y of the antiseptic cap and valve assembly shown in ; FIGS. 28-30 are side views in cutaway of two different embodiments of the antiseptic cap; FIGS. 31 a,b are, respectively, side views in cutaway showing an antiseptic cap with a centrally ed actuation post mounted on a valve with the valve in the unactivated and activated positions; FIGS. 32 and 33 are side views in y showing two different embodiments of an antiseptic cap having a molded sponge; is a side view in cutaway showing another embodiment of an antiseptic cap having a molded sponge docked to a valve; is a side View in cutaway showing a step of attaching a molded sponge to an antiseptic cap; is a side View in cutaway showing a step of delivering an antiseptic compound to a molded sponge positioned within a cap; shows a side View in cutaway of an antiseptic cap docking to a valve with the antiseptic cap having an antiseptic coating; shows a perspective View of an antiseptic cap in a blister package; is a side cross-sectional View of an antiseptic cap with a thread cover; is a side sectional View of an antiseptic cap with a thread cover; is a side cross-sectional view of an antiseptic cap with a thread cover; FIGS. 4Za,b are perspective front and back views of an antiseptic cap with a thread cover connected to a Cardinal SMART SITE access site; FIGS. 43 a,b are perspective front and back views of an ptic cap without a thread cover connected to a Cardinal SMART SITE access site; FIGS. 44 a,b are perspective front and back views of an antiseptic cap with a thread cover connected to a Hospira (ICU) C1000 Clave access device; FIGS. 45 a,b are perspective front and back views of an antiseptic cap without a thread cover connected to a Hospira (ICU) C1000 Clave access device; FIGS. 46 a,b are perspective front and back views of an antiseptic cap with a thread cover connected to a B. Braun ULTRASITE access device; FIGS. 47 a,b are perspective front and back views of an antiseptic cap without a thread cover connected to a B. Braun ULTRASITE access device; FIGS. 48 a,b are perspective front and back views of an antiseptic cap with a thread cover connected to a Rymed INVISION PLUS access device; FIGS. 49 a,b are perspective front and back views of an antiseptic cap t a thread cover connected to a Rymed INVISION PLUS access device; is a side cross-sectional View of an ptic cap with a thread cover connected to a Cardinal SMARTSITE PLUS access device; is a side sectional View of an antiseptic cap with a thread cover connected to a Cardinal ITE PLUS access device and the thread cover having a reduced er when compared to the thread cover shown in ; is a side cross-sectional View of an antiseptic cap with a thread cover connected to a Hospira (ICU) C1000 Clave access device having a thread cover with an alternative proﬁle; is an assembly view of an antiseptic cap and cup holder equipped plunger and e barrel system; is an assembly view of a cup—holder-antiseptic cap assembly adjacent a plunger and syringe barrel system; is a side view in cross—section of an antiseptic cap and cup holder equipped plunger and syringe barrel ly; a is a perspective View of a medical access device adjacent an antiseptic cap equipped plunger and syringe barrel assembly with a lid stock peeled back in preparation for g; b is a perspective view of a medical access device docked to an antiseptic cap equipped plunger and syringe barrel assembly; c is a perspective View of a medical access device docked to an antiseptic cap adjacent a plunger and syringe barrel assembly; is an ed View of a cup holder and antiseptic cap assembly adjacent an open and empty chamber of a syringe plunger; is an enlarged view of a cup holder and antiseptic cap assembly positioned within a chamber of a syringe plunger; is a perspective view of an alternative embodiment of an antiseptic assembly nt a syringe plunger and barrel assembly; is a perspective view of an alternative embodiment of an antiseptic assembly docked to a syringe plunger and barrel ly; is a perspective view of an alternative embodiment of an antiseptic assembly docked to a syringe plunger and barrel assembly with an outer wall being transparent to reveal interior portions of the ly; is a perspective view of a tip cap assembly having an ptic attached to a e; is a cross-sectional view of a tip cap having an antiseptic cap attached to a syringe; is an exploded, perspective View showing an antiseptic cap and a tip cap; is an exploded, perspective view showing an antiseptic cap holder assembly, a tip cap, and a syringe; is an exploded, perspective View g an antiseptic cap holder assembly, a tip cap, and a syringe; A is a cross-sectional view of an ptic cap assembly attached to a syringe; B is a sectional View of an antiseptic cap assembly and a e cap; is a side View of an antiseptic cap holder assembly attached to a tip cap attached to a syringe; is a perspective view of an antiseptic cap holder assembly; is a perspective view of a tip cap; is a cross-sectional view of the antiseptic cap holder assembly of and the tip cap of disengaged and unlocked; is a cross-sectional view of the antiseptic cap holder assembly of and the tip cap of engaged and locked; is a perspective view of a e having a plunger with a cap holder assembly that is ly removable from the plunger; is a cross—sectional View of the syringe, plunger, and cap holder assembly of ; FIGS. 75 and 76 are sequential views, showing the process of manually removing the cap holder ly from a chamber of the r; is a perspective view of another embodiment of a chamber of a plunger with ribs having grooves; is a cross-sectional view of the chamber of ; is a cross-sectional view of a cap holder assembly positioned within the chamber shown in ; is a cross-sectional view of a cap holder assembly partially removed from the chamber shown in ; is a cross-sectional view of another ment of a chamber of a plunger with ribs having two sets of grooves; is a sectional View of a cap holder assembly positioned within the chamber shown in ; is a cross—sectional View of a cap holder assembly partially removed from the chamber shown in ; is a perspective view of another embodiment of a plunger having sidewalls with recessed areas; is a perspective View of r embodiment of a plunger having two or more sidewalls positioned at angles of greater than ninety degrees from each other to provide access to the chamber; is a perspective view of another embodiment of a syringe having a ﬂange with receptacles for receiving a cap holder assembly; is a perspective View of the syringe shown in with a cap holder assembly positioned in a receptacle; is a perspective view of a ﬂange connector panel having a cap holder assembly receptacle and a ﬂange slot in a sidewall; is a top View of the ﬂange connector panel of connected to a gripping ﬂange of a syringe; is a perspective view of another embodiment of a ﬂange connector panel having a ﬂange slot in r ll; is a top view of the ﬂange connector panel of connected to a gripping ﬂange of a syringe; is a perspective View of another embodiment of a syringe with a gripping ﬂange having engagement teeth; is a perspective view of a ﬂange connector panel that engages with the gripping ﬂange of ; is a perspective View of another embodiment of a ﬂange connector panel for connection with a gripping ﬂange having a lip; is a perspective View of a ﬂange connector panel that attaches to the gripping ﬂange of ; is a perspective View of a plunger and cap holder ly connected by a frangible attachment; is a cross-sectional view of the plunger and cap holder assembly ofFIG. is an exploded view of a plunger having a transverse opening to receive a cap holder ly; is an exploded View of another embodiment of a plunger having a transverse g for receiving a cap holder assembly; 0 is a front View of the plunger of ; 1 is a side View of the plunger of ; 2 is a perspective View of another embodiment of a cap holder assembly having a locking ﬂange; 3 is a l ctive View of a plunger having a g chamber; 4 is a partial cross-sectional View of the cap holder assembly of 2 and the plunger of 3 disengaged and unlocked; is a cross-sectional view of the cap holder of the cap holder assembly of 2 and the plunger of3 engaged and locked; 6 is a perspective View of r embodiment of a plunger having a locking lever and a cap holder assembly disposed n; 7 is a cross-sectional view of the plunger and cap holder assembly of 6; 8 is a side View of the locking lever of FIGS. 106 and 107; 9 is a cross-sectional View of another embodiment of the plunger and cap holder ly that includes a g lever with a toe; 0 is a side View of the locking lever of 9; 1 is a side View of a cap holder ly and a plunger each having an adhesive material thereon; 2 is a side View of a cap holder assembly and a plunger with compressible material in an uncompressed state; 3 is a side View of a cap holder assembly and plunger with the compressible material in a compressed state; 4 is a cross—sectional View of a plunger and a cap holder assembly, wherein the cap holder assembly ﬂange is positioned a distance away from the plunger ﬂange; is an exploded View of a plunger having a locking ﬂange attached thereto and a cap holder assembly; 6 is a perspective View of the plunger and the cap holder assembly of 5 disposed in the r; 7 is a top View of the locking ﬂange of FIGS. 115 and 116; and 8 is a top View of another ment of the locking ﬂange of FIGS. 115 and 1 16. 2012/062078 DETAILED DESCRIPTION OF THE INVENTION While this invention is susceptible of embodiment In many ent forms, there is shown in the drawings, and will be described herein in detail, speciﬁc embodiments thereof with the understanding that the present disclosure is to be considered as an exempliﬁcation of the principles of the invention and is not intended to limit the invention to the speciﬁc embodiments illustrated.

FIGS. 1 and 2 show an antiseptic cap equipped plunger and syringe barrel assembly 10 having an antiseptic cap equipped r (or piston) ly 12 and a e barrel 14. The barrel 14 has a side wall 16 deﬁning a chamber 18 and the barrel has a proximal end 20 and a distal end 22. The proximal end 20 has an opening 23 to the chamber 18 and a ﬂange 24 extending radially outwardly from the wall 16. The ﬂange 24 has upper and lower surfaces 26, 28 and provides gripping surfaces for a user of the ly 10. The distal end 22 of the barrel 14 has an end wall 30 and an elongate tip 32 extending distally therefrom and having a passageway 34 therethrough and in ﬂuid communication with the chamber 18. The distal end wall 30, in one preferred form of the invention, is generally conically shaped and, as is well known in the art, can have a locking luer collar 35 concentrically surrounding the tip 32 and having a set of threads 37 on an inside surface thereof. The luer collar 35 allows for attaching a needle or a cannula to the syringe assembly and for docking the assembly to mating threads located on other s such as valves and injection sites. shows the syringe assembly proximate an access site 38 having a valve 39 controlling access to a lumen of a tubing 41.

In one preferred form of the invention the chamber 18 of the syringe assembly 10 will be ﬁlled with a locking solution or a ﬂush solution for use with an indwelling, central venous er. The manner of using a looking or ﬂush on with a er is well known in the art. Suitable locking or ﬂushing solutions will be set forth below. The ﬂush or locking solution is injected into a ﬂuid access site of the catheter to clean and disinfect the catheter and can be withdrawn from the catheter or d to remain in an end portion ofthe catheter to serve as a barrier to the s of pathogens and contaminants.

The antiseptic cap plunger assembly 12 has an elongate shaft 40, a proximal end 42 and a distal end 44. The elongate shaft 40, in one preferred form of the invention, is generally cruciform in cross—sectional shape. A stopper or piston 50 is connected to the distal end 44 of the plunger 12. The piston 50 is dimensioned such that when inserted into the e barrel chamber 18 an outer circumferential surface of the piston is in ﬂuid-tight engagement with an inner surface 54 of the syringe barrel. The piston assembly 12 when moved proximally (or when being withdrawn) can draw ﬂuid into the r and when moved distally (or when inserted into the syringe chamber) can drive ﬂuid out of the chamber. shows the piston assembly 12 partially inserted into the e chamber and shows the piston ly fully ed into the e chamber to deliver ﬂuid to the tubing 41.

A housing 60 is located at the proximal end of the plunger assembly 12 and has a wall 62 deﬁning a r 64 having an open end 66 which can be sealed by any suitable structure or material such as a cap or by a foil material 68. An al annular ﬂange 70 extends radially outwardly from the wall 62 and provides a surface upon which the sealing structure can be attached. shows a cap assembly 80 proximate the chamber 64 of the housing 60 and shows the cap assembly 80 positioned within the chamber 64. In one preferred form of the invention, the cap assembly 80 has a cap 82 having a wall 83 deﬁning a chamber 84 containing an absorbent material 86 such as a . The sponge 86, in a preferred form of the invention, is wetted or soaked with an agent such as an antiseptic, anticoagulant or antimicrobial (“antiseptic solution”) and can be selected from the locking and ﬂushing solutions set forth below or the antiseptic solutions set forth below. The cap 82 has an interior surface 87 with a set of threads 88 for mating with a set of threads on the access site 38.

FIGS. 7 and 8 show the cap ly 80 sealed with a foil material or lid stock material 68 which can be attached to the ﬂange 70 by any le method such as by adhesives or by conductive or inductive heat sealing techniques. shows the ptic cap piston assembly 12 and shows the antiseptic cap equipped piston assembly 12 inserted into the chamber of the syringe barrel 14 to deﬁne the antiseptic cap equipped piston and syringe barrel assembly 10.

FIGS. 3 and 4 show one possible method for utilizing the cap assembly 80 by docking with the access device 38. shows the lid stock 68 pealed away from the ﬂange 70 and shows docking the antiseptic cap assembly 80 to the valve 39. The syringe barrel is rotated clockwise or counterclockwise to engage the threads 88 of the antiseptic cap assembly 80 with the s of the access site 38. After engagement, the syringe barrel 14 will be moved away from the access site 38 and the antiseptic cap assembly 80 will slide outward from the housing 60 and remain docked to the access site 38. The antiseptic cap assembly 80 can remain docked to the valve 39 of the access site 38 for any suitable period of time from a few minutes to numerous hours. When the antiseptic cap ly 80 is docked to the valve 39 the tubing or catheter 41 is sealed to block the s into the catheter of pathogens and contaminants and a portion of the access site 38 is exposed to the antiseptic material in the sponge 86.

It is desirable that during the rotation of the syringe barrel that the antiseptic cap assembly 80 does not rotate with respect to the housing and/or optionally that the plunger assembly 12 does not rotate with respect to the syringe barrel 14 so that the s 88 of the antiseptic cap can fully engage the threads of the access site. The present invention provides a mechanism ated with the assembly 10 for preventing the rotation of the antiseptic cap assembly 80 with respect to the plunger assembly 12 and more preferably a mechanism on either the plunger assembly or on the ptic cap 80 to prevent relative rotational movement between the antiseptic cap 80 and the plunger assembly 12. In an even more preferred form of the invention, the mechanism for ting relative rotation of the antiseptic cap 80 with respect to the plunger assembly 12 has mating portions on both parts that when assembled cooperatively engage one another to prevent relative rotation. It is also contemplated that a separate mechanism, device or member could be used to lock the two parts together to achieve this e.

If a user of the assembly 10 grasps the assembly 10 by the antiseptic cap and plunger assembly 12 then the interlocking structures between the piston assembly 12 and the syringe barrel 14 would not necessarily be needed. Accordingly, FIGS. 5, 9-11 show ary structures for locking the antiseptic cap assembly 80 inside the housing 60 so that these parts rotate together and one part does not rotate in a direction or at a rate different from that of the other part. Further, FIGS. 15—18 show exemplary structures for interlocking the antiseptic cap plunger assembly 12 with the syringe barrel 14.

In one preferred form of the ion the housing 60 will have a e or structure that forms an interference ﬁt with an external e 83 of the antiseptic cap 80.

Even more preferably, an internal e 63 of the side wall 62 of the housing 60 will have a feature or ure to form an interference ﬁt with a portion of the antiseptic assembly 80. In another preferred form of the ion the antiseptic cap assembly 80 will have a feature to form an interference ﬁt with the housing 60 and even more preferably the outer surface 83 of the antiseptic cap 80 will have a feature to contact the inner surface 63 of the housing side wall 62.

WO 66742 2012/062078 In another preferred form of the invention the plunger housing 60 and the cap assembly 80 each will have a feature or structure that cooperatively engage one another to prevent relative rotation of the cap assembly 80 and the housing 60. shows one preferred form of the invention having a plurality of circumferentially spaced and axially extending ribs 100 on the internal surface 63 of the housing side wall 62 (internal ribs 100) for engaging the wall 83 of the antiseptic cap 82 to lock the cap assembly 80 in place to prevent rotation of the cap assembly 80 when positioned inside the housing 60. In a preferred form of the invention, the internal ribs 100 extend from a bottom wall 102 up to an intermediate height of the housing sidewall 62. In a preferred form of the invention the internal ribs 100 will have a height roughly equal to a height of the cap 82. A plurality of internal slots 108 are deﬁned between each set of adjacent internal ribs 100. The internal ribs 100, in a preferred form of the invention, will have a width that tapers inwardly from proximate the bottom wall 102 to a top 104 of the internal ribs 100 so that the width of the internal ribs decrease from a bottom 106 of a rib to the top 104 of the rib. Also, it is preferable that the top of the internal ribs 100 have a generally arcuate proﬁle to act as a lead-in during ion of the antiseptic cap assembly 80 into the housing 60. In a preferred form of the ion, the internal ribs 100 will terminate short of a top 113 of the housing sidewall 62 to deﬁne an annular gap 111 between the top of the rib 104 and the top 113. Also, extending radially inwardly from the internal e 63 of the cap 82 is a detent 109 positioned proximate a top portion 113 ofthe side wall 62.

The antiseptic cap 82 has a plurality of circumferentially spaced and axially extending ribs 120 extending along an external e 122 of the cap 82 (external ribs 120) from an annular ﬂange 123. The al ribs 120 are dimensioned for engaging a portion of the or wall of the housing 62 to t relative rotation of the cap and the plunger ly 12 and deﬁne a ity of external slots one of each between each adjacent pair of external ribs. When the cap 82 is positioned within the chamber 64 (FIGS. 9 and 11) each of the external ribs 120 are positioned within an internal slot 108 and each of the internal ribs are positioned within an external slot to lock together these parts to assure that the cap rotates in the same direction as the plunger rod. FIGS. 6 and 11 also show that when the cap 82 is positioned within the housing 60, the detent 109 contacts the annular ﬂange 123 to hold the cap in the g to prevent or resist inadvertent ng of the cap from the housing prior to docking of the cap with the access site. In one preferred form of the invention, the external ribs 120 are speciﬁcally designed in conjunction with internal slots 108 so that the antiseptic cap is guided out of the storage chamber 64 as the cap is screwed onto the s of the access site.

FIGS. 12- 14 show several embodiments of gripping surfaces on the housing 60 (with lid stock 68 removed) to facilitate use of the assembly 10 or the plunger assembly 12. shows axially extending and circumferentially spaced protuberances 130 on an outer surface of the wall 62. The erances 130 can have numerous different cross- sectional shapes including circular, polygonal, oval and irregular and, in a preferred form of the ion, extend from the ﬂange 70 to a bottom of the housing. shows a housing 60 that has no ﬂange 70 and has protuberances 130 on the wall 62 extending substantially the entire height of the g 60. shows a housing 60 where the outer surface of the wall 62 is relatively smooth but has a series of circumferentially spaced and axially extending protuberances 130 on a ferential edge of the ﬂange 70.

As with the cap and plunger assembly rotational locking features or structures, the optional plunger assembly 12 and syringe barrel 14 g feature or structure can be positioned alone on the plunger assembly 12, or alone on the syringe barrel 14 or have cooperating structures on both the plunger assembly 12 and the syringe barrel 14. It is also contemplated that a separate mechanism, device or member could be used to lock the two parts together to achieve this purpose.

FIGS. 15—18 show various embodiments for the optional feature of locking the plunger assembly 12 from rotational motion with respect to the syringe barrel 14. In one embodiment shown in FIGS. 15-17 and 21 a wing 150 extending axially along an e surface of the housing side wall 62 engages a tooth 152 positioned on an interior surface of the syringe barrel at is proximal end. More preferably, the plunger ly 12 will have more than one wing 150 with each wing being circumferentially spaced from the other. In an even more preferred form of the invention the plunger assembly will have four wings 150 spaced 90 s from one another. Also, in a more preferred form of the invention, the syringe barrel will have a plurality of circumferentially spaced teeth. When the plunger assembly is nearly fully inserted into the syringe barrel each of the wings will extend into a tooth to prevent rotation of the plunger assembly 12 with respect to the syringe barrel 14. shows another embodiment of a locking feature to prevent rotation of the plunger assembly 12 with respect to the syringe barrel 14 and also prevents ve ational motion of the parts. In this embodiment an annular protuberance 160 positioned on an interior surface of the syringe barrel at its proximal end 20 engages an annular detent 162 on an outside surface of the plunger rod.

FIGS. 19 and 20 Show an antiseptic cap equipped plunger assembly 12 and non- reﬂuxing e assembly 170. ﬂuxing es are well known in the art and there are numerous methodologies for reducing reﬂux while accessing the access site of a central venous catheter. In this embodiment the annular ﬂange 70 of the plunger assembly 12 abuts the ﬂange 24 of the syringe barrel prior to the piston 50 contacting an or surface of the syringe distal end wall 30.

It is contemplated that the antiseptic cap assembly 80 of the present invention need not be coupled or combined with a plunger or a syringe barrel. FIGS. 223, b show a stand-alone antiseptic cap assembly 200 having three circumferentially spaced ribs 120 for grasping by the hand of a user of the cap assembly. a shows the cap 82 without an absorbent material 86 and b shows the cap with an absorbent material. The cap 200 can be used for the same purposes of the cap assembly 80 described above but will be used by hand. All other features of the cap 200 are ially the same as described above with the exception that the cap 200 does not have to be dimensioned to ﬁt within a chamber carried by a syringe plunger. FIGS. 23 and 24 show varying frequency of ribs 120 and varying shapes and sizes. shows the cap 200 proximate the access site 38 and FIGS. 26 and 27 show the cap 200 docked to the access site 38.

A suitable absorbent material 86 es medical grade materials capable of storing and releasing an antiseptic liquid, or liquid having other medical purposes, and includes materials such as sponges, rupturable capsules and other als or devices capable of serving this purpose. Suitable sponges can include any sponge suitable for use for medical purposes and can be naturally occurring or synthetic. The sponges can be die cut into suitable shapes or can be molded into the desired shape. It is desirable that the sponge 86 be attached to the antiseptic cap 82 to t the sponge 86 from rtently falling out of the cap 82. shows the sponge 86 is captured between an annular wall 202 and a disc 204 attached to the cap 82 by any suitable method such as ultrasonic or vibrational welding or other techniques well known in the art.

FIGS. 29 and 30 show a variation on the cap assembly 200 of . In this ment, the sponge is retained in the cap 82 with a plastic sheet 206 heat welded to the cap. In one preferred form of the invention the sponge is attached by an adhesive or by other method to form an assembly which is then attached to the cap.

FIGS. 31 a, b show the cap 200 having a coaxially disposed and axially ing actuating post 220 circumferentially surrounded by a sponge 86 having a centrally oned hole to ﬁt over the post 220. 3 shows the cap 200 in initial engagement with the access site 38 and b shows the cap threaded onto the access site 38 and the actuating post opens the valve 39 and antiseptic ﬂuid is d to ﬂow into the valve.

FIGS. 32-34 show varying shaped sponges that, in one red form of the invention, were molded into various desirable shapes. The sponge of has a l opening 230 to tate attaching the sponge to the cap and to ﬁlling the sponge with antiseptic, anticoagulant or other suitable ﬂuids set forth above. shows the cap having a centrally disposed energy director 231, an ultrasonic welder 232 being brought into cooperative engagement with the sponge on a side of the sponge te the energy director 231. By applying ultrasonic energy the energy director 231 melts and attaches the sponge to the cap. shows a ﬁlling device 240, having a lumen 242 and a dispensing head 244 in ﬂuid communication with a source of antiseptic, anticoagulant or the like for dispensing a metered amount of such ﬂuid into the interior portion of the sponge. shows an alternative embodiment of the antiseptic cap 200 where the sponge is replaced by an antiseptic coating on the actuating post 220. shows the antiseptic cap 200 positioned in a blister pack 233 prior to sealing the blister pack. shows an antiseptic cap 300 with a thread cover 302. The thread cover 302 can be part of any of the antiseptic caps sed herein. The thread cover 302 is made of a deformable material capable of ﬂexing upon application of moderate force applied by hand. In one preferred form of the invention the thread cover 302 is made from a polymeric ning material and more preferably a polymeric material having a modulus of elasticity of less than 20,000 psi. In another preferred form of the invention the ric material will be an elastomer or plastomer or like material. The thread cover 302 es the connection between the antiseptic cap 300 and a device such as a valve or other access devices 38. The thread cover 302 provides a physical barrier to the ingress of pathogens, dust or other contaminants through the mating threads of the antiseptic 300 and the access device or valve to which it is docked. The thread cover 302 also serves to retain antiseptic ﬂuids from the antiseptic cap 300 from leaking out through the threads.

The thread cover can be made a part of the antiseptic cap 300 using techniques well known in the art such as overmolding, or by attaching as a separate part using welding techniques such as heat conductive welding, heat induction g, vibrational welding, stretch or friction ﬁt, or by using a suitable adhesive.

The thread cover 302 can provide a universal ﬁt to most commercially available valves, connectors and access devices, or the thread cover 302 can be customized to dock with a particular access . shows, as is described above, the antiseptic cap 300 has an r wall 305 having a ﬁrst end 306 and a second end 320 with the ﬁrst end having a greater diametrical dimension than the second end. The annular wall deﬁnes a central r 322 having an open end 323. In one preferred form of the invention, the chamber 322 will have a sponge 86 positioned therein as shown in and 6 above, although it is not shown in . The thread cover 302 is shown attached by an optional g layer 304 to the ﬁrst end 306 of the annular wall 305. The thread cover 302 has a ﬁrst leg 308 and a second leg 310. The ﬁrst leg 308 extends parallel to the annular wall 305 and the second leg 310 extends radially ly from the annular wall 305 in a direction transverse to the ﬁrst leg 308 and across a portion of the open end 323 and deﬁnes a central opening 312, having a reduced er when compared to the open end 323, into the chamber 322. The second leg 310 terminates at a distal end 330 with a rounded outer surface 332. shows an alternative embodiment of the antiseptic cap 300 having the thread cover 302 having both the ﬁrst and second legs 308, 310 attached to the ﬁrst end 306 of the annular wall 305 through bonding layers 304 a,b. A top surface 340 of the ﬁrst end 306 is shown having the same thickness or diametrical dimension as the remainder of the ﬁrst end but it is contemplated the top surface could have a radially extending ﬂange 123 as shown in shows an alternative embodiment of the antiseptic cap 300 that differs from the ptic cap shown in FIGS. 39 and 40 by not including a counterbore 336 shown in these ﬁgures. The counterbore 336 es a chamber of reduced diameter and, therefore, will form a tighter ﬁt with access devices with a narrower outer diameter when compared to the cap shown in which does not include the counterbore. This is just one example of the modiﬁcations that can be made to the geometry of the antiseptic cap to enhance the connection between the cap and an access site.

FIGS. 42a,b show front and back views of the antiseptic cap 300 with the thread cover 302 connected to a Cardinal SMART SITE access site 350. FIGS. 43 a,b are perspective front and back views of the antiseptic cap without the thread cover 302 connected to the al SMART SITE access site.

FIGS. 44a,b are perspective front and back views of the antiseptic cap 300 with the thread cover 302 connected to a Hospira (ICU) C1000 Clave access device 352. FIGS. 4Sa,b are perspective front and back views of the antiseptic cap, without a thread cover 302, connected to the Hospira (ICU) C1000 Clave access device.

FIGS. 46a,b are perspective front and back views of the antiseptic cap 300 with the thread cover 302 connected to a B. Braun ULTRASITE access device 354. FIGS. 47a,b are perspective front and back views of the antiseptic cap without the thread cover 302 connected to the B. Braun ULTRASITE access device.

FIGS. 4Sa,b are perspective front and back views of the antiseptic cap with the thread cover 302 ted to a Rymed ON PLUS access device; 356. FIGS. 49a,b are perspective front and back views of the antiseptic cap without the thread cover 302 connected to a Rymed INVISION PLUS access device.

FIGS. 50-52 show various embodiments of the thread cover 302. differs from in that the second leg 310 extends farther across the opening of the chamber in than shown in . shows another embodiment of the thread cover 302 having a segmented second leg 310a,b. This embodiment may be ble to provide a more effective seal for certain access devices. shows an exploded view of an ative embodiment 400 of the syringe barrel assemblies 10, discussed above, orating a cap holder 402 into the system of parts. Thus, the alternative ly and system 400 has an antiseptic cap and cap holder equipped plunger assembly 12’, a syringe barrel 14, an antiseptic cap 82 (shown with an optional thread cover 302), an absorbent material 86, and peelable lid stock 68. shows an exploded View of an antiseptic cap holder assembly 404 including the cap holder 402 with the antiseptic cap assembly 80 positioned within a chamber 406 of the cap holder 402. This embodiment 400 allows for the separate manufacture, ly, and ization of the assembly 400 from the plunger assembly and the syringe barrel.

The cap holder 402 has a al and distal ends 408, 410, and an inner wall surface 412 and an outer wall e 414, an opening 416 into the chamber 406, and a radially outwardly extending ﬂange 418 circumjacent the opening 416 and extending from the proximal end 408 of the cap holder 402. The cap holder 402 will also have an optional bottom wall 419.

In a preferred form of the invention, the cap holder 402 or the antiseptic cap 82 will have a structure, element or the like that prevents the relative rotation of the cap holder 402 and the antiseptic cap 82 until the antiseptic cap ly 80 is securely docked to the access device 38. Also, in a preferred form of the invention the cap holder 402 or the r assembly 12’ will have a structure, element or the like for preventing the relative rotation of the cap holder 402 and the r assembly 12’ until the antiseptic cap assembly 80 is securely docked to the access device 38. Any of the anti-rotation devices discussed above to stop the rotation of the antiseptic cap assembly 80 with the plunger assembly 12 would be suitable for, these purposes. Also, it is contemplated the devices discussed above in reference to FIGS. 15-21 to prevent the relative rotation of the plunger assembly 12 and the syringe barrel 14 could be incorporated into this embodiment 400. shows the inner wall surface 412 of the cap holder 402 carries the al ribs 100 and the internal slots 108 that interact with the external ribs and external slots 120, 122 of the cap 82 as is described above with respect to These structures t or resist the relative rotation of the cap holder 402 with respect to the ptic cap assembly 80. The term “ribs” referred to herein are structures that are raised or extend outward from a surface. The term “slots” refer to structures that extend below a surface or is deﬁned n two ribs and is at a lower level than the ribs. also shows an interlocking structure for preventing the relative rotation of the cap holder 402, or the cap holder assembly 404, with respect to the plunger assembly 12’. The outer wall surface 414 has a plurality of circumferentially spaced and axially extending ribs 420 deﬁning slots 424 between each pair of adjacent ribs. In a preferred form of the invention, the ribs 420 are generally triangular in shape having a base portion 426 and an apex portion 428. The slots 424 are oppositely—oriented triangularly shaped areas having slot base portions 430 ing between two adjacent rib apex portions 428 and slot apex portions 432 separating adjacent rib base portions 426. On the al wall surface 63 of the plunger chamber 64 are rly shaped plunger ribs 434 and r slots 436. The ribs 420 are dimensioned to ﬁt within the plunger slots 436 and the slots 424 are dimensioned to ﬁt over and receive the plunger ribs 434. Thus, when the cap holder 402 or the cap holder assembly 404 is inserted in the plunger chamber 64 the cap holder ribs 420 are interdigitated with the plunger ribs 434 to prevent or resist the relative rotation of the cap holder 402, or cap holder assembly 404, with respect to the plunger assembly 12’.

In yet another preferred form of the invention, the cap holder 402, the cap holder assembly 404 or the plunger assembly 12’ will have a structure, element or the like that resists the relative axial movement of these parts when the cap holder 402 or the cap holder assembly 404 is positioned fully within the plunger assembly 12’. In one red form of the ion the cap holder 402 has an annular protuberance 440 that is dimensioned to ﬁt within an annular groove 442 on the inner wall surface 414 of the cap holder and preferably extends in line with the base portions of the plunger ribs 434. A second locking structure is provided having a ity of teeth 450 which extend axially outward from the outer wall surface 414 of the cap holder and are positioned in slots 424. In a preferred form of the ion the teeth extend axially outwardly to a height beyond the height of the ribs 434. The teeth 450 can be positioned in one or more of the slots or in each of the slots 424 or in alternating slots or, as is shown, circumferentially spaced 90° from one another. The teeth 450 preferably are positioned at an intermediate portion, between the base and the apex, of a slot 424. The teeth 450 are dimensioned to ﬁt within a segmented annular groove 452 that s circumferentially about the inner surface 412 ng through the plunger ribs 434 at an intermediate portion, between the base and the apex, of the plunger ribs 434.

FIGS. 56a,b,c tively show the assembly 400 in a ready-for-use position, docked position, and used position. The assembly 400 is used in essentially the same fashion as bed above with t to FIGS. 3 and 4 except that when the assembly 400 is in the used position the cap holder 402 s in the plunger assembly 12’.

The syringe barrel and plunger can be fabricated from any material suitable for its purpose and includes glass and polymeric al. Suitable polymeric materials include, but are not limited to, homopolymers, copolymers and terpolymers formed from monomers such as oleﬁns, cyclic oleﬁns, amides, esters, and ethers. The polymeric material may be a blend of more than one polymeric al and can be a monolayer structure or a multilayer ure. In one preferred form of the invention the syringe barrel and the plunger are injection molded from a polypropylene material. 2012/062078 FIGS. 59-61 show a third embodiment 500 of an antiseptic cap equipped syringe r and barrel assembly with the antiseptic cap ly 80 and lid stock 68 removed for clarity. The third embodiment 500 provides for retroﬁtting an antiseptic cap assembly 502 to a standard plunger 504. The antiseptic cap 502 has a ﬁrst generally cylindrical outer wall 506 having a proximal end 508 and a distal end 510. The proximal end 508 is removably or ﬁxedly attached to a button 512 of the r 504. The proximal end has an g 514 dimensioned to ﬁt about the button 512 and has a member for attaching to the button. In one red form of the invention, the attaching member includes a plurality of circumferentially spaced, and axially inwardly ed tabs 516 extending from an inner wall surface 518 and the tabs engage a lower surface of the button 512 to attach the antiseptic cap assembly 502 to the plunger 504.

The distal end of the antiseptic cap 502 has a top annular ﬂange 520 extending radially inwardly from the ﬁrst cylindrical wall 506 and deﬁnes a generally circular opening 522. A second cylindrical wall 524 extends axially downwardly from the top annular ﬂange 520 and is coaxially disposed within the ﬁrst cylindrical wall 506. When the antiseptic cap 502 is attached to the plunger button 512 a bottom peripheral edge of the second cylindrical wall 524 will abut a top surface of the plunger button 512 thereby capturing, by oppositely ed y forces, the plunger button 512 between the tabs 516 and the second rical wall. It is contemplated, however, that a second set of tabs could be provided spaced axially away from the ﬁrst set of tabs and the piston button 512 could be trapped between the two sets of tabs. Further, it is contemplated other attaching means could be used that are well know in the art and the attaching member shown is merely exemplary.

The second cylindrical wall 524 deﬁnes a chamber as is shown in greater detail in above with the ribs and slots as described for engaging the antiseptic cap assembly 80 to prevent relative rotational movement and to resist relative axial movement of the parts when the antiseptic cap ly 80 is fully inserted into the chamber. Further, it is contemplated adapting the plunger and e as described above to t or resist the relative rotational movement of the plunger with respect to the barrel.

The piston 50 can be formed from any suitable material including a polymeric material or a silicone material. The stopper can be selected from a material with a desired durometer so that reﬂux is reduced when the stopper engages an inner surface of the distal end wall of the syringe barrel. le locking and ﬂush solutions include a lower alcohol selected from l, propanol and butanol. The locking solution can be a single lower alcohol or a blend of lower alcohols.

Suitable locking solutions can also include a lower l with an antimicrobial and or an anticoagulant. le locking solutions can contain at least one lower alcohol in a range from 1% to 99% by volume and at least one other anti-microbial and/or anti— coagulant compound in a range from 1% to 99% by volume. The lower alcohol will usually be in aqueous solution, typically at 1% to 99% by volume, usually from 5% to 95% by volume. The at least one other anti-microbial is selected from the group consisting of taurolidine and san, and the at least one anti-coagulant is selected from the group consisting of riboﬂavin, sodium e, ethylene diamine tetraacetic acid, and citric acid.

In one red form of the invention, the syringe assembly 10 will be pre-ﬁlled with one of the locking solutions and will be packaged by a manufacture and shipped to a health care provider. A cannula or needle will be attached to the distal end of the barrel and placed into ﬂuid communication with the ﬂuid access site of an indwelling central venous er. The ﬂush solution will be injected into the catheter to clean or lock the catheter. Afterwards, the cap assembly 80 will be removed from the plunger 17 and the cap will be docked to the ﬂuid access site of the catheter.

Citrate salt containing antiseptic solutions In one form, the antiseptic is a solution a citrate salt and in another form of the invention the citrate salt solution is a hypertonic solution. The term hypertonic is used herein to refer to a ﬂuid having an osmotic concentration and a y greater than the osmotic concentration and density of the blood of the patient. The antiseptic solution preferably comprises a citrate salt with a concentration range, in weight percent, of from about 1.5% to about 50% with an osmolality of about 300 to about 6400 mOsm. More preferably, the antiseptic solution ses citrate salt in a concentration range of from about 10% to about 40%, yet more preferably, in a concentration range of from about 20% to about 30%.

In a preferred embodiment, the antiseptic solution is prepared to have a pH lower than that of the pH of the patient's blood. The citrate salt solution may be prepared to have a pH lower than about 6.5, more preferably, from about 4.5 to about 6.5. Also, the citrate salt solution can e pharrnaceutically able agents such as sodium de and sodium heparin. The citrate salt solution can also include a variety of other antibacterial, antimicrobial and anticoagulant agents such as gentamicin, vancomycin, and mixtures of these agents. Additional anticoagulant agents include, for example heparin, urokinase, tissue plasminogen activation (tPA) and mixtures of these agents.

By “pharmaceutically acceptable,” it is meant that the citrate salt solution and the included salts and other additives which are, within the scope of sound l judgment, suitable for use in contact with tissues ns and lower animals without undue toxicity, irritation, and allergic response. It is also typically necessary that a composition be ized to reduce the risk of infection.

Antibacterial agent containing antiseptic solutions An antimicrobial agent containing antiseptic solution of the present invention may contain at least one l, at least one antimicrobial agent and at least one chelator and/or anticoagulant. Various antimicrobial substances as sed herein and that are well known to one of ordinary skill in the art may be combined with the g solution in order to inhibit infection. The crobial locking solution of the present invention may be use for ﬁlling or ﬂushing a medical device such as an indwelling device such as an implanted catheter. Other medical devices that are contemplated for use in the t invention are disclosed herein.

In another preferred form of the invention, the antiseptic agent can contain antibacterial agents such as those classiﬁed as aminoglycosides, beta lactams, quinolones or ﬂuoroquinolones, macrolides, sulfonamides, sulfamethaxozoles, tetracyclines, treptogramins, oxazolidinones (such as linezolid), clindamycins, lincomycins, rifamycins, glycopeptides, ins, lipo-peptide antibiotics, as well as pharmacologically acceptable sodium salts, pharmacologically acceptable calcium salts, pharmacologically acceptable potassium salts, lipid formulations, derivatives and/or analogs of the above.

The aminoglycosides are bactericidal antibiotics that bind to the 308 ribosome and inhibit bacterial protein synthesis. They are typically active against aerobic gram-negative bacilli and staphylococci. ary aminoglycosides that may be used in some speciﬁc aspects of the invention include amikacin, kanamycin, gentamicin, tobramycin, or netilmicin.

Suitable beta s are selected from a class of antibacterials that inhibit bacterial cell wall sis. A ty of the ally useful beta-lactams belong to either the penicillin group (penam) or cephalosporin (cephem) . The beta—lactams also include WO 66742 the carbapenems (e.g., imipenem), and ctams (e.g., aztreonam). Inhibitors of beta— lactamase such as clavulanic acid and its derivatives are also included in this ry.

Non—limiting examples of the penicillin group of antibiotics that may be used in the solutions of the present invention include amoxicillin, ampicillin, benzathine penicillin G, carbenicillin, illin, dicloxacillin, piperacillin, or ticarcillin, etc. Examples of cephalosporins include fur, ceftioﬁir sodium, cefazolin, cefaclor, ceftibuten, ceﬁizoxime, cefoperazone, cefuroxime, cefprozil, ceftazidime, xime, cefadroxil, cephalexin, cefamandole, cefepime, cefdinir, cefriaxone, ceﬁxime, cefpodoximeproxetil, cephapirin, cefoxitin, cefotetan etc. Other examples of beta s include mipenem or meropenem which are extremely active parenteral antibiotics with a spectrum against almost all gram-positive and gram—negative sms, both aerobic and anaerobic and to which Enterococci, B. fragilis, and P. aeruginosa are particularly tible.

Suitable beta ase inhibitors include clavulanate, sulbactam, or tazobactam.

In some aspects of the t invention, the antibacterial solutions may comprise a combination of at least one beta lactam and at least one beta lactamase inhibitor.

Macrolide antibiotics are another class of bacteriostatic agents that bind to the SOS subunit of ribosomes and inhibit ial protein synthesis. These drugs are active against aerobic and anaerobic gram-positive cocci, with the exception of enterococci, and against gative bes. Exemplary macrolides include erythromycin, azithromycin, clarithromycin.

Quinolones and ﬂuoroquinolones typically function by their ability to inhibit the activity of DNA gyrase. Examples include nalidixic acid, cinoxacin, trovaﬂoxacin, oﬂoxacin, levoﬂoxacin, grepaﬂoxacin, trovaﬂoxacin, sparﬂoxacin, norﬂoxacin, ciproﬂoxacin, moxiﬂoxacin and gatiﬂoxacin.

Sulphonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. These drugs inhibit lication of ia by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Examples include mafenide, sulﬁsoxazole, sulfamethoxazole, and sulfadiazine.

The tetracycline group of antibiotics include tetracycline derivatives such as tigecycline which is an investigational new drug (IND), minocycline, doxycycline or demeclocycline and analogs such as otetracycline, chlorotetracycline, or epioxytetracycline.

Suitable streptogramin class of antibacterial agents include quinupristin, dalfopristin or the combination oftwo streptogramins.

Drugs of the rifamycin class typically inhibit DNA-dependent RNA rase, leading to suppression of RNA synthesis and have a very broad spectrum of activity against most gram-positive and gram—negative bacteria including Pseudomonas nosa and cterium species. An exemplary rifamycin is rifampicin.

Other antibacterial drugs are glycopeptides such as vancomycin, teicoplanin and tives thereof. Yet other antibacterial drugs are the xins which are exempliﬁed by colistin.

In addition to these several other antibacterial agents such as prestinomycin, mphenicol, trimethoprim, fusidic acid, metronidazole, bacitracin, Spectinomycin, nitrofurantion, daptomycin or other leptopeptides, oritavancin, dalbavancin, ramoplamin, de etc. may be used in preparing the antiseptic solutions described herein. Of these, metronidazole is active only against protozoa, such as Giardia lamblia, Entamoeba histolytica and Trichomonas lis, and strictly anaerobic bacteria. Spectinomycin, is a bacteriostatic otic that binds to the 30S subunit of the ribosome, thus inhibiting bacterial n synthesis and nitrofurantoin is used orally for the treatment or prophylaxis of UTI as it is active against Escherichia coli, Klebsiella-Enterobacter species, staphylococci, and enterococci.

In other embodiments, the antimicrobial agent is an antifungal agent. Some exemplary s of ngal agents include imidazoles or triazoles such as clotrimazole, miconazole, ketoconazole, econazole, butoconazole, omoconazole, oxiconazole, terconazole, itraconazole, ﬂuconazole, voriconazole, posaconazole, nazole or ﬂutrimazole; the polyene antifungals such as amphotericin B, mal amphoterecin B, natamycin, nystatin and nystatin lipid formulations; the cell wall active cyclic lipopeptide antifungals, including the echinocandins such as caspofungin, micafungin, anidulfungin, cilofungin; LY121019; LY303366; the allylamine group of antifungals such as terbinaﬁne.

Yet other miting examples of antiﬁingal agents include naftiﬁne, tolnaftate, mediocidin, idin, trichomycin, hamycin, aurefungin, ascosin, ayfattin, azacolutin, trichomycin, levorin, heptamycin, candimycin, griseofulvin, BF—796, MTCH 24, BTG- 137586, pradimicins (MNS 18184), benanomicin; ambisome; nikkomycin Z; ﬂucytosine, or perimycin.

In another preferred form of the invention, the antimicrobial agent is an antiviral agent. Non-limiting examples of antiviral agents include cidofovir, amantadine, rimantadine, vir, gancyclovir, pencyclovir, famciclovir, foscamet, ribavirin, or lovir. In some forms of the invention the antimicrobial agent is an innate immune peptide or proteins. Some ary classes of innate peptides or proteins are transferrins, lactoferrins, defensins, phospholipases, lysozyme, cathelicidins, cidins, iocidal permeability increasing proteins, amphipathic alpha helical peptides, and other synthetic crobial ns.

In other embodiments of the invention, the antimicrobial agent is an antiseptic agent. Several antiseptic agents are known in the art and these e a taurinamide derivative, a phenol, a quaternary ammonium surfactant, a chlorine-containing agent, a quinaldinium, a lactone, a dye, a thiosemicarbazone, a quinone, a carbamate, urea, salicylamide, carbanilide, a guanide, an amidine, an oline biocide, acetic acid, benzoic acid, sorbic acid, propionic acid, boric acid, dehydroacetic acid, sulfurous acid, vanillic acid, esters of oxybenzoic acid, isopropanol, propylene glycol, benzyl alcohol, chlorobutanol, phenylethyl alcohol, 2-bromo—2-nitropropan-l,3—diol, formaldehyde, glutaraldehyde, m hypochlorite, potassium hypochlorite, sodium hypochlorite, iodine (in s solvents), povidone-iodine, hexamethylenetetramine, noxythiolin, 1-(3- choroallyl)—3,5,7-triazo l—azoniaadamantane chloride, taurolidine, taurultam, tr0 furfurylidene)-l-amino—hydantoin, 5-nitroﬁ1raldehyde semicarbazone, 3,4,4'- trichlorocarbanilide, 3,4',5-tribromosalicylanilide, 3—triﬂuoromethyl-4,4'— dichlorocarbanilide, oxyquinoline, 1-cyclopropylﬂuoro-l,4-dihydro—4-oxo(1- piperazinyl)—3 -quinolinecarboxylic acid, 1,4-dihydro-l-ethyl-6—ﬂuoro—4-oxo—7—( 1 - piperazinyl)—3—quinolinecarboxylic acid, hydrogen peroxide, peracetic acid, phenol, sodium oxychlorosene, parachlorometaxylenol, 2,4,4'—trichloro-2'-hydroxydiphenol, thymol, chlorhexidine, benzalkonium chloride, cetylpyridinium chloride, silver sulfadiazine, or silver nitrate.

In another preferred form of the invention, the antiseptic solution includes a basic t and a dye. The basic reagent may be a guanidium compound, a biguanide, a bipyridine, a phenoxide antiseptic, an alkyl oxide, an aryl oxide, a thiol, a halide, an aliphatic amine, or an aromatic amine. In some speciﬁc aspects, the basic reagent is a guanidium compound. Non- limiting examples of guanidium compounds e chlorhexidine, alexidine, hexamidine. In other speciﬁc embodiments, the basic reagent is a bipyridine. One example of a bipyridine is octenidine. In yet other aspects, the basic reagent is a phenoxide antiseptic.

The dye may be a lmethane dye, a monoazo dye, a diazo dye, an indigoid dye, a xanthene dye, an anthraquinone dye, a quinoline dye, an FD&C dye. Non—limiting examples of triarylmethane dye include gentian violet, crystal violet, ethyl violet, or brilliant green. ary monoazo dyes include FD&C Yellow No. 5, or FD&C Yellow No. 6. Other non-limiting examples of FD&C dye include Blue No. l or Green No. 3.

One non-limiting example of diazo dyes is D&C Red No. 17. An example of an indigoid dye is FD&C Blue No. 2. An example of a xanthene dye is FD&C Red No. 3; of an anthraquinone dye is D&C Green No. 6; and of an quinoline dye is D&C Yellow No. 1.

Other examples of ptics that may be used to the solutions of the invention are the phenoxide antiseptics such as clofoctol, chloroxylenol or triclosan. Still other ptic agents that may be used to prepare the amntimicrobial solutions of the invention are gendine, genlenol, genlosan, or genfocto].

One of skill in the art will iate that one can use one or more of the crobial agents including one or more antibacterial agent, and/or one or more antiﬁmgal agent, and/or one or more antiviral agent, and/or one or more ptic agent, and/or combinations thereof.

A wide variety of or agents are contemplated as useful in preparing the antiseptic ons of the invention. This includes chelators such as EDTA free acid, EDTA 2Na, EDTA. 3Na, EDTA 4Na, EDTA 2K, EDTA 2Li, EDTA 2NH4, EDTA 3K, Ba(II)-EDTA, Ca(II)-EDTA, Co(II)-EDTACu(II)—EDTA, Dy(III)-EDTA, Eu(III)-EDTA, Fe(III)—EDTA, —EDTA, La(IIl)—EDTA, CyDTA, DHEG, diethylenetriamine penta acetic acid (DTPA), DTPA-OH, EDDA, EDDP, EDDPO, EDTA-OH, EDTPO, EGTA, HBED, HDTA, HIDA, IDA, MethylEDTA, NTA, NTP, NTPO, O-Bistren, TTHA, EGTA, DMSA, deferoxamine, dimercaprol, zinc citrate, a combination of bismuth and citrate, penicillamine, succimer or Etidronate. It is contemplated that any chelator which binds barium, calcium, cerium, cobalt, copper, iron, ium, manganese, nickel, ium, or Zinc will be acceptable for use in the present invention.

Alternatively, one may use at least one anticoagulant such as heparin, hirudin, EGTA, EDTA, urokinase, streptokinase, hydrogen peroxide etc., in the preparation of the antimicrobial solutions of the invention. 2012/062078 In addition to the alcohols set forth above, a variety of alcohols are contemplated as useful in the preparation of the instant antiseptic solution, and include any antimicrobially active alcohol. Non—limiting es of alcohols include ethanol, methanol, isopropanol, propylene glycol, benzyl alcohol, chlorobutanol, ethyl alcohol, and the like.

One of skill in the art will appreciate that the ons of the instant ion can comprise various combinations of at least one alcohol, at least one antimicrobial agent, and at least one chelator/anticoagulant. In some speciﬁc embodiments, the solution of the invention comprises at least one alcohol, at least one tetracycline and at least one or/anticoagulant. In a speciﬁc aspect, such an antimicrobial solution comprises ethanol, at least one tetracycline and EDTA or n.

In other speciﬁc aspects, such a solution comprises ethanol, minocycline and EDTA or heparin. In one ment of this aspect, the concentration of minocycline is 0.001 mg/ml to 100 mg/ml. In another embodiment, the tration of minocycline is about 3 mg/ml. In r aspect, the concentration of EDTA is in the range of 10-100 mg/ml. In one embodiment of this aspect, the concentration ofEDTA is about 30 mg/ml.

In another preferred form of the invention, the antiseptic solution includes a pharmacologically able sodium salt, a pharmacologically acceptable calcium salt, a pharmacologically acceptable potassium salt and about one milligram per milliliter polyhexamethylene biguanide hydrochloride in an aqueous ure. Additionally, the solution of the invention may also contain a pharmacologically acceptable salt of lactic acid.

Salt containing antiseptic solutions One preferred antiseptic solution includes a pharmacologically acceptable sodium salt such as sodium chloride or the like in a concentration of between about 820 mg to about 900 mg, a pharmacologically acceptable calcium salt, such as calcium de dihydrate or the like in a concentration between about 30.0 mg to about 36.0 mg, a pharmacologically acceptable potassium salt, such as potassium chloride or the like in a concentration between about 28.5 to about 31.5 mg and about one milligram per milliliter polyhexamethylene biguanide hydrochloride in an aqueous admixture with one hundred milliliters of water for injection U.S.P. For ular applications, the solution of the invention may also include sodium lactate in a concentration between about 290 mg and about 330 mg in the one d milliliter aqueous admixture.

Photo—oxidant ons In another red form of the present invention, the antiseptic solution contains an anticoagulant and a photo-oxidant. In certain embodiments, a photo—oxidant is selected that has an antiseptic effect. As used , the term “photo-oxidant” is intended to refer to a compound (usually an organic dye) that has photo—oxidation properties, in which the compound exhibits an increased oxidizing potential upon exposure to radiant energy such as light. The term “photooxidan ” also refers to a composition that releases one or more electrons when struck by light.

In one preferred aspect of the ion, the photo-oxidant is ene blue, which advantageously provides otic and antifungal activity, and also provides a color to make the antiseptic solution clearly identiﬁable. In addition to methylene blue, other photo-oxidants may include Rose Bengal, hypericin, methylene violet, proﬂavine, rivanol, vine, toluide blue, trypan blue, neutral red, a variety of other dyes or mixtures thereof. Therefore, in ate aspects of the invention, one or more alternative photo- oxidants, preferably a colored photo—oxidant is used in ance with the invention in place of methylene blue. ed Viscosity solutions In another preferred form of the invention, the antiseptic solution includes a low Viscosity antibacterial agent mixed with a ity increasing agent. Examples of antibacterial agents which may be used, in addition to those bed above, se alcohols, chlorhexidine, Chlorpactin, iodine, tauroline, citric acid, and soluble citric acid salts, particularly sodium citrate, optionally mixed with water.

Suitable Viscosity increasing agents include Carbopol, starch, methylcellulose, carboxypolymethylene, carboxymethyl cellulose, hydroxypropylcellulose, or the like.

Carbopol is a cross-linked polyacrylic acid based polymer sold by Noveon, Inc. It is ably neutralized to about pH 7 with a base material such as tetrahydroxypropyl ethylene diamine, triethanolamine, or sodium hydroxide. Derivatives of starch may also be used, such as hydroxyethylstarch, hydroxypropylstarch, or starch having bonded organic acid ester groups, to improve compatibility with antibacterial agents such as alcohols, for example, ethanol or isopropanol. Such ester groups may be the reaction product of two to twelve carbon organic acids with the starch, for example. Also, the elevated viscosity antiseptic solution may be created by the use of a fat emulsion, or other dispersions in water/alcohol of glycerol mono or di esters of fatty acids, or fatty acid esters of other polyols such as sugars having one or more bonded fatty acid groups per molecule.

Analogous compounds with ether linkages may also be used.

Also, other materials such as alginic acid, with or without m citrate may be used, or polyvinyl l, with or without borax, povidone, polyethylene glycol alginate, sodium alginate, and/or tragacanth. If desired, the ﬂuid of this invention may also contain an effective amount of an antithrombogenic agent such as heparin, and a diluent such as water, along with other desired ingredients.

In one preferred form of the ion, the ptic solution contains a mixture of isopropyl alcohol and neutralized Carbopol, with other optional ients being present such as water, antithrombogenic agents such as heparin, and the like. Preferably, about 0.4 to 2 weight percent of Carbopol is present. Citric acid may also be present as an antibacterial agent, either with or as a substitute for another anti—bacterial agent such as pyl alcohol or ethanol.

In another embodiment, the antiseptic solution is a gel of an isopropyl alcohol, optionally with up to about 30 weight percent water, and about 2.2 weight percent hydroxypropylcellulose, to form a high ity antiseptic solution.

In yet another preferred form of the invention, the antiseptic solution contains carbohydrates and/or glucose degradation ts. Suitable carbohydrates are chosen form the group of e and/or fructose. Suitable degradation products include 3- deoxyglucosone (3-DG), acetaldehyde, formaldehyde, dehyde, glyoxal, methylglyoxal; 5-hydroxymethyl—2- furaldehyde (S-HMF), 2-furaldehyde, and 3,4- dideoxyglucosone—3-ene GE).

Other suitable agents to be used in this embodiment of the antiseptic solution includes substances having agulatory properties i.e., inhibitors of the coagulation cascade such as heparin of standard and low molecular weight, onated heparin, synthetic inhibitors in the coagulation cascade, Futhan as a broad protease inhibitor, complexing and chelating substances such as citrate, EDTA, EGTA, nces and mixtures used for preservation of blood products (platelets or plasma), CDPA (citrate, sodium phosphate, dextrose, adenine), synthetic or natural thrombin inhibitor substances.

Other suitable additives include dan, riboﬂavin, vitamin E, alphatocopherol, folic acid and amino acids. Furthermore, antiinﬂammatory compounds and drugs could also be used, e.g. cortison, mycophenolic acid (MPA) and derivates thereof, sirolimus, tacrolimus and porin, diclofenac, etc.

Inhibitory peptides can also be used in the antiseptic solution such as defensins, (dermacidine), and others. Radicals, such as reactive e species, NO-releasing systems or nitric oxide (NO), and peroxynitrite may also be used. A buffer composition may also be included in the antiseptic on, and in one red form of the invention, the buffer contains lactate, bicarbonate, pyruvate, ethyl pyruvate and citric acid in combination and mixtures including adjustment of pH by acetic acid, hydrochloric acid or sulphuric acid. Furthermore, viscosity enhancing additives may be added, such as lipids or lipidic substances (also to get water insoluble ns or complexes into solution), nutrients in high concentration density gradient e.g. aminoacid containing ﬂuids, polyglucose, lcodextrin, pectine, yethyl starch (HES), alginate, hyaluronic acid, etc.

Taurolidine antiseptic solutions and gels The ptic solutions of the present invention can include Taurolidine and/or tam to prevent clotting and Bioﬁlm formation or the elements can be combined with other antimicrobial agents. One embodiment of the present invention is a gel with thixotropic ties to keep the solution inside the antiseptic cap and not spill out during the time interval between uses. This is accomplished by making a hydrogel matrix as a drug delivery vehicle containing a biocompatible antimicrobial agent alone or with another active agent, which may be useful for particular purposes. The hydrogel matrix is biocompatible and, biodegradable in the bloodstream. The matrix can be a hydrogel (e.g., , n, etc), a protein (e.g., collagen, hemoglobin, etc), a colloidal substance (e.g., serum albumin etc.), an on or other adjuvant. Preferably, the matrix shall have structural integrity and be thixotropic. Thixotropy is a property, which is exhibited by certain gels. It is a property characterized by a solid or semisolid substance that when shaken, d or subject to high shear forces becomes ﬂuid like and can ﬂow and then returns to the semisolid state when the forces and/movement are stopped. Alternatively, the gel could have the properties similar to that of the colloidal dispersion which resists movement, or ﬂow until a high shear force is imparted to the ﬂuid and then it ﬂows easily.

Other ingredients may be added to the gel matrix to provide further functional beneﬁt. The preferred antimicrobial is Taurolidine, which can be added to the matrix as a micro le powder, or encapsulated in liposomes, microspheres, or heres. It should be appreciated that numerous active agents and drugs can be added to the thixotropic gel ing sterileants, lysing agents (such as Urokinase), imaging enhancers, catheter surface modiﬁers, antibiotics and antimicrobial chemicals.

A hydrogel comprises a three-dimensional molecular network containing large quantities of water giving them good biocompatibility with material consistency that is soft solid-like with high diffusive properties to gases, chemicals and proteins. Suitable hydrogels include natural polymers including serum albumin, collagen, or alginates, polyvinyl alcohol, poly (ethylene oxide) or poly (hydroxyethylene) and polyelectrolytes, such as poly(acrylic acid), poly(styrene sulfonate), and carboxymethylcellulose (CMC).

One preferred form of the ptic solution includes idine with Salicylic acid or Sodium Salicylate in an aqueous solvent. Salicylic Acid and Sodium Salicylate are drugs that have been used with antibiotic locks in catheters to enhance the biocidal action of the otic alone and to inhibit the attachment of microbes to surfaces. This last attribute is ally important because the initiation of a Bioﬁlm expression and growth require that the individual bacteria must ﬁrst attach lves to the underlying surface.

By stopping attachment, Bioﬁlm formation is blocked.

Sodium salicylate has been trated to have remarkable antibacterial activity, including the ability to enhance the activities of certain antibiotics. This drug inhibits adherence, growth and Biofilm formation.

EDTA containing ptic solutions In one preferred antiseptic solution of the t invention provides antimicrobial, antifungal, anti-Viral and anti-amoebic properties and may also serve as an anti—coagulant.

Speciﬁed salts and compositions of ethylene diamine tetraacetic acid (EDTA) (C10H12N2Na403) are used at specified concentrations and pH levels.

The EDTA ations of the present invention are safe for human stration and are biocompatible and non—corrosive. They may also have anticoagulant properties and are thus useful for preventing and/or treating a variety of catheter—related infections.

In one embodiment, antiseptic solutions of the present ion have at least four, and preferably at least ﬁve, of the following properties: anticoagulant ties; inhibitory and/or bactericidal activity against a broad spectrum of bacteria in a planktonic form; tory and/or ﬁmgicidal activity against a spectrum of fungal pathogens; inhibitory and/or bactericidal ty against a broad spectrum of bacteria in a sessile form; inhibitory activity against protozoan infections; inhibitory activity against amoeba infections; safe and biocompatible, at least in modest volumes, in contact with a t; safe and biocompatible, at least in modest volumes, in a t's bloodstream; and safe and compatible with industrial objects and surfaces. The antiseptic solution can have a pH higher than physiological pH such as a pH of >8.0, or at a pH >8.5, or at a pH>9, or at a pH>9.5.

In another preferred form of the invention, the antiseptic solution contain a sodium EDTA salt (or ation of sodium salts) in solution at a pH in the range between 8.5 and 12.5 and, in another embodiment, at a pH of between 9.5 and 11.5 and, in yet r embodiment, at a pH of between 10.5 and 11.5.

When used herein, the term “EDTA salt” may refer to a single salt, such as a di- sodium or tri—sodium or tetra-sodium salt, or another EDTA salt form, or it may refer to a combination of such salts. The composition of EDTA ) depends both on the EDTA salts used to formulate the composition, and on the pH of the composition. For antiseptic solutions of the present ion consisting of sodium EDTA salt(s), and at the desired pH ranges (speciﬁed above), the sodium EDTA salts are predominantly present in both the tri- sodium and tetra-sodium salt forms.

In one embodiment, the antiseptic solution contains a combination of at least the dium and tetra-sodium salts of EDTA, and more ably solutions containing at least 10% of the EDTA in the composition is present in the tetra-sodium salt form. In yet another embodiment, at least 50% and, more preferably at least 60%, of the EDTA in the composition is present in the tri—sodium salt form.

EDTA solutions of the present invention are preferably provided in a sterile and non-pyrogenic form and may be packaged in any convenient fashion. The compositions may be prepared under sterile, aseptic ions, or they may be sterilized following preparation and/or packaging using any of a variety of suitable sterilization techniques.

Formulation and production of antiseptic compositions of the present invention is lly straightforward. In one embodiment, desired antiseptic solutions of the present invention are formulated by dissolving one or more EDTA salt(s) in an aqueous solvent, such as ed water, to the desired concentration and ing the pH of the EDTA salt solution to the desired pH. The antiseptic solution may then be sterilized using conventional means, such as autoclaving, UV irradiation, tion and/or ltration, and other means. The preferred osmolarity range for EDTA solutions is from 240-500 mOsM/Kg, more preferably from 300-420 mOsrn/Kg. The solutions are preferably formulated using USP materials.

Antiseptic solutions containing sodium salts of EDTA other than tri- and tetra- sodium salts, such as di-sodium EDTA, is also contemplated. For example di-sodium WO 66742 2012/062078 EDTA solutions can be used but such solutions have a lower pH in solution than the desired pH range of compositions of the present invention but, upon pH adjustment to the desired range using a pH adjustment material, such as sodium hydroxide, sodium acetate, and other well-known pH adjustment agents, EDTA solutions prepared using di-sodium salts are converted to the preferred combination di— and/or tri— and/or tetra-sodium salt EDTA solutions of the present invention. Thus, different forms and combinations of EDTA salts may be used in the preparation of EDTA compositions of the present invention, provided that the pH of the composition is adjusted to the desired pH range prior to use. In one embodiment, antiseptic compositions consisting of a mixture of primarily tri—and tetra- sodium EDTA is provided by dissolving di-sodium EDTA in an aqueous solution, 3%—5% on a weight/volume basis, and adding sodium hydroxide in a volume and/or tration sufﬁcient to provide the desired pH of>8.5 and <12.0.

Antibacterial enzyme containing ptic solutions “Antibacterial enzyme” refers to any proteolytic, orming, degradative or inhibitory enzyme that kills or damages a bacterial species or particular strain thereof. The result may be achieved by damaging the cell wall of the bacteria, disrupting cell membranes associated with the cell wall or within the bacteria, inhibiting protein synthesis within the bacteria, disrupting the sugar backbone, or by any other mechanism attributed to a peptide or protein ered by those skilled in the art to be an cterial enzyme.

The enzyme may be a l, wild-type enzyme, modiﬁed by conventional techniques, conjugated to other molecules, inantly expressed, or synthetically constructed.

One example of an antibacterial enzyme is lysostaphin. aphin is important because it is effective in the treatment of staphylococci and bioﬁlms formed therefrom.

“Lysostaphin,’ 3 and “lysostaphin analogues” are deﬁned as including aphin (wild type), any lysostaphin mutant or variant, any recombinant, or related enzyme (analogue) or any synthetic version or fragment of lysostaphin (whether tic or otherwise) that retains the lytic ability, in vivo and in vitro, to cleave the cross-linked polyglycine bridges in the cell wall peptidoglycan of staphylococci. The enzymes may be generated by post-translational processing of the protein (either by enzymes present in a producer strain or by means of enzymes or reagents introduced at any stage of the s) or by mutation of the structural gene. Mutations may include site deletion, ion, domain removal and replacement mutations. 2012/062078 The lysostaphin may be synthetically constructed, expressed in mammalian cells, insects, bacteria, yeast, reptiles or fungi, recombinantly expressed from a cell culture or higher recombinant species such as a mouse, or otherwise. This would e the activity-retaining synthetic construction including tic peptides and polypeptides or recombinant expression of portions of the lysostaphin enzyme responsible for its activity against staphylococci as part of a larger protein or peptide, e chimeric proteins, containing the active sites of one or more other antibacterial enzymes that are effective either against staphylococci or other bioﬁlmforming ia species.

The antibacterial enzymes may also be coated on the surface of the s described herein by immersion of the device in a on of the enzyme for a length of time sufﬁcient to form a bioﬁlm—formation inhibiting coating of the enzyme on the susceptible surface. Even the most minimal concentration of enzyme will confer some protection. Typically, a concentration of from about 10 pg/ml to about 100 mg/ml can be used. With device surfaces, the coatings may also be formed by nt attachment of the enzyme thereto.

Antiseptic coatings It is contemplated that the devices described herein can be coated with an antiseptic coating by any suitable technique such as immersion of the part into an antiseptic on, by spray coating the part with the antiseptic solution, by blending the antiseptic solution or material into the ric material used to fabricate the device.

In one preferred form of the invention, a quantity of logical, antimicrobial metal compound is added to the resin for direct molding of an article. Physiological, antimicrobial metals are meant to include the precious metals, such as silver, gold and platinum, and copper and zinc. Physiological, antimicrobial metal compounds used herein e oxides and salts of preferably silver and also gold, for example: silver acetate, silver benzoate, silver carbonate, silver citrate, silver chloride, silver iodide, silver nitrate, silver oxide, silver sulfa diazine, silver sulfate, gold chloride and gold oxide. Platinum nds such as chloroplatinic acid or its salts (e.g., sodium and calcium chloroplatinate) may also be used. Also, compounds of copper and zinc may be used, for , example: oxides and salts of copper and zinc such as those indicated above for silver.

Single physiological, antimicrobial metal compounds or combinations of physiological, antimicrobial metal compounds may be used.

Preferred physiological, antimicrobial metal compounds used in this invention are silver acetate, silver oxide, silver sulfate, gold chloride and a combination of silver oxide and gold chloride. The particles of the silver compounds are sufﬁciently able to be extracted to form a zone of inhibition to prevent and kill bacteria growth.

In another preferred form of the invention the devices herein are impregnated with san and silver compounds or triclosan and exidine.

Referring to FIGS. 62 and 63, a syringe having a tip cap with an antiseptic cap ed thereon is generally indicated at 610. This ement facilitates use of the antiseptic cap by providing the cap in a convenient location at the proper time it can be used. The syringe 612 includes a barrel 614 having a forward end 616. The forward end of the syringe 612 is red with an access point connection 618 for ment to an access point to deliver a ﬂuid or medicament to a t. Prior to use, the syringe access point connection 618 is covered with a tip cap 620. The tip cap 620 has a proximal end 621 that is attached to the access point tion of the syringe 612. The tip cap 620 also has a distal end 641 that carries an antiseptic cap 82. The antiseptic cap 82 could contain an absorbent material such as a sponge 86. The sponge 86 could be made from bonded ﬁber such as the bonded ﬁber material which is ble from Filtrona Porous Technologies, based in Richmond, VA. The sponge 86 can store an antiseptic liquid.

As can be seen in FIGS. 62 and 63, a cap assembly 680 is sealed by a cover or ﬁlm 650 which is ed to the surface of the tip cap 620 such as to a ﬂange 648. A pull tab 652 may be provided for facilitating removal of the ﬁlm 650 to provide access to the antiseptic cap 82.

Referring to , it can be seen that the tip cap 620 has proximal and distal chambers 622 and 642 respectively, positioned within a cylindrical or tapered side wall 624. The side wall 624 is shown to be continuous but it could have discrete areas of different sizes to accommodate chambers of different sizes. The side wall 624 could e ribs or gripping surfaces to facilitate ng thereof. The proximal chamber 622 is conﬁgured for attachment to the access point connection 618 on the forward end 616 of the barrel 614 of the syringe 612 as is known. As shown, the proximal chamber 622 of the tip cap 620 receives and releasably engages the central male extension of the access point connection 618, as well as the annular surface that extends thereabout. The conﬁguration of the proximal chamber 622 can be varied in accordance with what is known in the art.

The proximal chamber 622 could have a base wall 626.

The distal chamber 642 is sized and conﬁgured to receive an antiseptic cap 82. The distal chamber 642 could have a base wall 646. As with the plunger equipped antiseptic cap previously described, the antiseptic cap 82 could have one or more ribs 643 as shown in , and the inner wall of the distal chamber 642 could have corresponding ribs 645 to prevent relative rotational movement between the distal chamber 642 and the antiseptic cap 82.

In use, a syringe with an antiseptic cap 82 is provided with a ﬂuid or medicament for ry to a patient through an access point. The tip cap 620 is removed from the syringe 612 and the syringe 612 is ted to the access point and ed to deliver the ﬂuid or medicament. The syringe 612 is then disconnected from the access point, the tip cap 620 is accessed, and the pull tab 652 is used to remove the cover 650 to provide access to the ptic cap 82. Then, gripping the tip cap 620, one places the antiseptic cap 82 on the access point and pushes and/or twists the antiseptic cap 82 onto the access point. Once the antiseptic cap 82 is attached to the access point, the tip cap 620 can be removed such that the antiseptic cap 82 is withdrawn from the distal chamber 642 and remains attached to the access point where it disinfects and protects the access point until the next time the access point is accessed. shows another aspect of a tip cap 720 wherein a distal chamber 742 is conﬁgured to receive a cap holder assembly 780 having an antiseptic cap. The tip cap 720 has a al end 721 and a distal end 741. In this aspect, the distal r 742 is conﬁgured in accordance with the ration of the chamber of the plunger equipped antiseptic cap previously described and receives the cap holder assembly 780 n. The antiseptic cap can be used as discussed previously, or the cap holder assembly 780 can be removed from the tip cap 720 and used directly. shows another aspect of a tip cap 820 wherein a distal chamber 842 is conﬁgured to receive a cap holder assembly 880 having an antiseptic cap. The tip cap 820 has a proximal section 821 and a distal section 841. As illustrated, the proximal section 821 and the distal section 841 can be two discrete ns of varying shape and size. For example, the proximal section 821 could have a cylindrical or tapered side wall, as shown.

The discrete ns of varying shape or size can accommodate chambers of ent sizes. Further, the discrete sections, e.g., the proximal section 821 and the distal section 841, could include ribs 843 or gripping surfaces to facilitate handling thereof. In this aspect, the tip cap 820 is conﬁgured to change geometry from the proximal section 821 to the distal section 841. Speciﬁcally, the proximal section 821 is shown to have a truncated conical shape and red to attach to the access point connection 618 of a syringe 612, while the distal section 841 is designed and conﬁgured to receive the cap holder assembly 880. The cap holder assembly 880 may have ribs 845 that coact with ribs 843 on the distal chamber 842 to prevent rotation of the cap holder assembly 880 with respect to the tip cap 820. The antiseptic cap can be used as discussed previously, or the cap holder assembly 880 can be removed from the tip cap 820 and used directly.

A is a cross-sectional view showing a syringe with an antiseptic cap assembly 9803 disposed thereon generally indicated at 910. The syringe 912 includes a barrel 914 having a forward end 916. The forward end 916 of the syringe 912 is conﬁgured with an access point connection 918 and a rical wall 919 for attachment to an access point to deliver a ﬂuid or medicament to a patient. Prior to use, the syringe access point connection 918 is covered with a cap assembly 98021 that engages the cylindrical wall 919. The cap assembly 980a includes an antiseptic cap 982a and a ﬂexible ring 984a. The ﬂexible ring 9843 could be formed by an extension of the outer surface 983 of the cap assembly 980 or, the ﬂexible ring 984a could be in the form of a ﬂexible cap having a top 985b and a circular ring 987b with a cap assembly 980b attached to the top 985b, as shown in B. The cap assembly 980 is attached to the cylindrical wall 919 of the e 612 by stretching the ﬂexible ring 984 around the cylindrical wall 919 such that the ﬂexible ring 984 forms around and engages the cylindrical wall 919. The ﬂexible ring 984 is biased s a normal er that is smaller than, or equal to, the diameter of the cylindrical wall 919, such that the cap assembly 980 is secured to the syringe 912. is a side view g a syringe with an antiseptic cap assembly attached to a tip cap disposed n generally ted at 1010. The syringe 1012 includes a barrel 1014 having a forward end 1016. The forward end 1016 of the syringe 1012 is red with an access point connection for attachment to an access point to deliver a ﬂuid or medicament to a patient. Prior to use, the syringe access point connection is covered with a tip cap 1020. The tip cap 1020 has a al end 1021 that is attached to the access point connection of the syringe 1012. The tip cap 1020 also has a distal end 1041 comprising a snap—ﬁt ﬂange 1042. A cap holder assembly 1080 s an antiseptic cap 1082 and includes a snap-ﬁt chamber 1084 located at a bottom thereof. The snap—ﬁt chamber 1084 is conﬁgured to mate with the snap-ﬁt ﬂange 1042. In use, the antiseptic cap 1082 could be applied while the antiseptic cap holder assembly 1080 is attached to tip cap 1020 or the antiseptic cap holder assembly 1080 can be removed from the tip cap 1020 and used separately.

Referring to FIGS. 69-72, a tip cap and cap holder assembly combination are generally indicated at 1110. The tip cap 1120 has a proximal end 1121 that is attached to the access point connection of a syringe and a distal end 1141 comprising a distal end wall 1149 having a distal locking chamber 1142 disposed therein. A cap holder assembly 1180 has a proximal end 1181. The proximal end 1181 of the cap holder assembly 1180 es a locking protrusion 1160 comprising a stem 1162 and a locking ﬂange 1164, discussed in greater detail below.

Referring to FIGS. 71 and 72, it can be seen that the tip cap 1120 es a proximal chamber 1122 and the distal locking chamber 1142 positioned within a cylindrical or tapered side wall 1124. The side wall 1124 could e ribs or gripping es to facilitate handling thereof. The proximal chamber 1122 is conﬁgured for attachment to an access point connection on a forward end of a barrel of a syringe as is known. The conﬁguration of the al chamber 1122 can be varied in accordance with what is known in the art.

The distal locking chamber 1142 comprises a circular chamber having an oblong or oval entrance 1154. The locking ﬂange 1164 on the locking protrusion 1160 of the cap holder assembly 1180 has an oblong or oval shape conﬁgured to match the shape of the ce 1154 of the distal locking chamber 1142. The stem 1162 preferably has a wall thickness that s the distal end wall 1149 of the tip cap 1120. This conﬁguration allows the locking ﬂange 1164 to be inserted into the distal locking chamber 1142. After the locking ﬂange 1164 is inserted into the distal locking chamber 1142, the cap holder assembly 1180 can be rotated, such as by 90 degrees, such that the locking ﬂange 1164 rotates in the ar distal locking chamber 1142, to retain the locking ﬂange 1164 in the chamber 1142 such that the locking ﬂange 1164 cannot be pulled therefrom because of the oblong or oval entrance 1154. In such an arrangement, the cap holder ly 1180 is locked to the tip cap 1120 until it is rotated an additional 90 degrees. antly, other locking ﬂange 1164 and ce or cut out 1154 geometries are contemplated, and they are not limited to solely oblong or oval geometries. Instead, the locking ﬂange 1164 and the entrance or cut out 1154 may be ng asymmetrical designs, rectangular, triangular, or any other geometric arrangement. In use, the antiseptic cap 1182 could be applied while WO 66742 2012/062078 the antiseptic cap holder ly 1180 is ed to the tip cap 1120 or the antiseptic cap holder assembly 1180 can be removed from the tip cap 1120 and used separately.

Referring to FIGS. 73-76, a syringe assembly having a plunger conﬁgured for removably receiving an antiseptic cap is shown generally at 1210. As shown in FIGS. 73 and 74, the syringe 1210 has a barrel 1214 and a plunger 1240. The plunger 1240 has a proximal end 1242 that includes a chamber 1260, sized to receive and removably hold a cap holder assembly 1220. Referring to , the chamber 1260 is deﬁned by a bottom wall 1261, and an annular sidewall 1262 that has a peripheral proximal end 1266 that deﬁnes an opening 1268 through which the cap holder assembly 1220 can be inserted into the chamber 1260.

The cap holder ly 1220, as previously discussed herein, comprises a cap holder 1222, an antiseptic cap 1282, a sponge 1286 in some cases, an antiseptic material, and a cover or ﬁlm 1250. A pull tab 1252 could be ed for facilitating removal of the ﬁlm 1250 from the cap holder 1222 to e access to the ptic cap 1282. The cap holder 1222 could have a distal end 1224 and one or more bulges 1228 on the outer surface 1226 to secure the cap holder assembly 1220 in the chamber 1260.

The sidewall 1262 of the plunger 1240 includes one or more apertures 1270 deﬁned by edges 1272. The one or more apertures 1270 provide access to the chamber 1260 and facilitate removal of the cap holder assembly 1220 from the plunger 1240 as will be described hereinafter.

The cap holder assembly 1220 can be removed from the plunger 1240 and the process thereof is shown in FIGS. 75 and 76. As shown in , removal of the cap holder assembly 1220 from the r 1240 involves placing one’s thumb or ﬁnger through the one or more apertures 1270 against a lower surface of the the cap holder assembly 1220. As shown in , one thereafter pushes against the cap holder assembly 1220 with a ﬁnger or thumb to urge the cap holder assembly 1220 out of the chamber 1260. Ultimately, the cap holder assembly 1220 is ejected from the chamber 1260. In this way, the antiseptic cap 1282 could be conveniently used at a different time than the syringe 1210.

FIGS. 77-80 show another embodiment of a chamber 1360 of a plunger 1340 wherein an interior surface 1374 of the chamber 1360 of the plunger 1340 could have a plurality of circumferentially spaced ribs 1376 that contact the cap holder assembly 1320 to secure the cap holder assembly 1320 in the chamber 1360. As shown in FIGS. 77-80, the ribs 1376 could each contain a ﬁrst groove 1378 shaped to accept the bulge 1328 of the cap holder 1322 to further secure the cap holder assembly 1320 within the chamber 1360.

As such, applying pressure to the cap holder assembly 1320, disengages the bulge 1328 from the groove 1378, as shown in . Further pressure against the cap holder assembly 1320 continues the removal process. The ribs 1376 could also be tapered to facilitate the lled removal of the cap holder assembly 1320, and prevent the cap holder assembly 1320 from ejecting too rapidly. The ribs 1376 can provide a decreasing amount of resistance against the bulge 1328 of the cap holder 1322 as the cap holder assembly 1320 is urged out of the chamber 1360.

FIGS. 81-83 show another embodiment of a chamber 1460 of a plunger 1440.

Like the chamber 1360 of the plunger 1340, the chamber 1460 includes a plurality of ribs 1476. In this embodiment the ribs 1476 of the chamber 1460 could each contain a ﬁrst groove 1478 and a shallower second groove 1480 closer to the proximal end 1466 of the chamber 1460 and shaped to accept the bulge 1428 of the cap holder 1422 of the cap holder assembly 1420. As shown in FIGS. 82 and 83, as the cap holder assembly 1420 is urged out of the chamber 1460, the bulge 1428 disengages the ﬁrst groove 1478, and then, after continued pressure, engages the second groove 1480, and then is removed entirely.

The second groove 1480 facilitates the controlled ejectment of the cap holder assembly 1420 from the chamber 1460 because less force is required to disengage the cap holder assembly 1420 from the second groove 1480 than from the ﬁrst groove 1478. is a ctive View showing a plunger 1540 having four support walls 1530 extending at 90 degree angles with respect to each other from a common point.

Towards the proximal end 1542 of the plunger 1540, one or more support walls 1530 has a recessed area 1532 proximal the one or more apertures 1570 to facilitate removal of the cap holder assembly by providing more clearance for a user to place his or her thumb beneath the cap holder assembly as previously shown in FIGS. 75 and 76. The ost edge of the recessed area 1532 is closer to the common point than the outermost edge of the rest of the ll 1530. The recessed area 1523 could be deﬁned by a ﬂat edge 1532a, sloped edge 1532b, or both, as shown in . shows a plunger 1640 having a ﬁrst set of four support walls 1630 at 90 degrees with t to each other positioned at a distal portion of the plunger, and a second set of four support walls 1634 at a proximal n 1642, some of which are spaced apart at a r angle with t to each other to allow a wider aperture 1670 in WO 66742 the sidewall 1662 of the chamber 1660. At least two of the support walls ﬂank the aperture of the r, which facilitates access to, and removal of, the cap holder assembly by providing more clearance for a user’s ﬁnger or thumb or other removal too], if any.

Shown in FIGS. 86 and 87 is a syringe having a gripping ﬂange 1715 with one or more storage acles. Speciﬁcally, the gripping ﬂange 1715 of the syringe 1710 includes one or more fully or partially bounded apertures 1717 capable of receiving and g a cap holder assembly 1720 and/or a pre-cleaner 1721. The pre-cleaner 1721 could be used where an access site was not previously disinfected by an antiseptic cap of the present invention, if at all. In such a circumstance, the pre—cleaner 1721 would disinfect the access site, the access site would be used, and then the antiseptic cap would be applied. The cap holder assembly 1720 can be attached within the aperture by a friction ﬁt and the ﬂange about the cap opening can contact the syringe gripping ﬂange 1715, or the cap holder ly could be otherwise engaged within the aperture.

Referring to FIGS. 88-95, ﬂange tor panels for receiving a cap holder assembly can be attached to standard gripping ﬂanges of syringes. As shown in FIGS. 88 and 89, a ﬂange connector panel 1846 could have an aperture capable of ing and holding a cap holder ly. As shown, the aperture 1817 could have a portion along the outer edge of the ﬂange connector panel 1846 that is unbounded, or the aperture could be completely bounded by the ﬂange connector panel 1846 (not shown). The ﬂange connector panel 1846 includes a slot 1856 in a sidewall 1854 providing access to a sleeve portion 1848. The sidewall 1854 and sleeve portion 1848 are red to receive a portion of a gripping ﬂange 1815 of a syringe and thereby attach the connector panel 1846 to the syringe. For example, the gripping ﬂange 1815 is curved, and sleeve n 1848 is similarly curved. This attachment could be maintained by a friction ﬁt, or other means.

FIGS. 90 and 91 show a similar device having an re 1917, where the slot 1956 providing access to the sleeve portion 1948 to receive a portion of the gripping ﬂange 1915 is on another sidewall of the connector panel 1946.

In another embodiment, shown in FIGS. 92 and 93, a ﬂange connector panel 2046 comprises an aperture 2019 completely d by the ﬂange connector panel 2046, and capable of receiving and holding a cap holder assembly. The ﬂange connector panel 2046 includes a slot 2056 providing access to a sleeve portion 2048 having sockets 2049. The sockets 2049 correspond in shape and on to engagement teeth 2023 on a gripping ﬂange 2015 extending from the perimeter of the gripping ﬂange 2015. In this way, when the ﬂange connector panel 2046 is engaged with the gripping ﬂange 2015, the engagement teeth 2023 are received by the sockets 2049 to retain the ﬂange connector panel 2046 on the gripping ﬂange 2015. The teeth 2023 of the gripping ﬂange can have two different sides: a gradually angled side 2029a, farthest from the r 2040, and a sharply angled side 2029b. The sockets 2049 can have corresponding angles. The gradually angled sides 20293 of the teeth 2023 and s 2049 provide for easy engagement of the connector panel 2046 to the gripping ﬂange 2015, which the sharply angled sides 2029b of the teeth 2023 and s 2049 prevent disengagement, y locking the connector panel 2046 to the gripping ﬂange 2015.

In a further embodiment, shown in FIGS. 94 and 95, a gripping ﬂange 2115 includes a lip 2125 along its outer perimeter. A ﬂange connector panel 2146 that includes an re 2119, a ﬁrst pair of ﬁngers 2149a, and a second pair of ﬁngers 2149b extending from the bottom of the connector 2146 and conﬁgured to connect to the lip 2125 of the gripping ﬂange 2115. The distance between the ﬁrst pair of ﬁngers 2149a and second pair of ﬁngers 2149b could correspond to the width of the lip 2125 of the gripping ﬂange 2115, such that the ﬁrst and second pair of ﬁngers 2149a, 2149b bear against the lip 2125 of the gripping ﬂange 2115. The ﬁrst pair of ﬁngers 2149a could contact the top surface of the gripping ﬂange 2125. The second pair of ﬁngers 2149b could be longer than the ﬁrst pair of ﬁngers 2149a and comprise ﬂanges 2151 conﬁgured to extend down and contact the bottom surface of the of the gripping ﬂange 2115. Additionally, as shown, the four ﬁngers 2149a, 2149b are in a rectangular formation. However, the ﬁngers could be of varying numbers, sizes (e.g., length or width), and/0r ions, such as two , six ﬁngers, or a trapezoidal ion.

FIGS. 96 and 97 show a cap holder assembly 2220 connected to the proximal end 2242 of plunger 2240 by a frangible attachment 2236. The frangible ment 2236 can be made of plastic, and a user can remove the cap holder assembly 2220 from the plunger 2240 by breaking the frangible attachment 2236, such as by bending or twisting. In this way, the cap holder assembly 2220 could be conveniently used at a different time than the syringe 2210. The cap holder 2222 could have an annular protrusion 2238 extending from its distal end 2224 and encircling the frangible attachment 2236 to protect a user from contact and potential injury from the frangible attachment 2236 after breaking the frangible attachment 2236.

WO 66742 is a perspective view of a plunger 2340 having a receptacle 2333 extending transverse to the plunger 2340. As in previous embodiments, the plunger 2340 has four support walls 23303, 2330b, 2330c, and 2330d extending at 90 degree angles with respect to each other from a common point. One t wall 2330b has a discontinuance deﬁned by end walls 2335a and 2335b. The support wall 2330d on the opposite sides has an internal recess deﬁned by distal end wall 23350, lateral end wall 2335d, and proximal end wall (not shown). Transverse support walls 2330a and 23300 have an inner circular wall 23350 forming an aperture that extends through walls 2330a and 23300 between the tinuance in wall 2330b and the recess in wall 2330d, creating a receptacle in the plunger. The receptacle is shaped to e a cap holder assembly 2320. Arrow A illustrates the path of insertion of the cap holder assembly 2320 into the receptacle in the plunger. As shown, the receptacle is circular, but the receptacle could be a variety of shapes. The lateral end wall 2335d of the cutout provides structure and rigidity and prevents over insertion of the cap holder ly 2320. The cap holder assembly 2320 can be retained in the plunger 2340 by a friction ﬁt, or other means.

Shown in FIGS. 99-101 is a plunger 2440 having a receptacle 2433 at a proximal end extending transverse to the plunger 2440. The plunger 2440 has four support walls 2430a, 2430b, 2430c, and 2430d ing at 90 degree angles with respect to each other from a common point. Support walls 2430a and 24300 deﬁne the receptacle 2433 and could be square or rectangular to odate a square or rectangular cap holder of the cap holder assembly 2420. Arrow B illustrates the path of ion of the plunger cap holder ly 2420. Support wall 2430b has a break providing clearance for engagement of the cap holder assembly 2420 with the receptacle 2433. The support walls 2430 could include a cutout deﬁning sidewalls 2435a and a bottom wall 2435b. As with the previous embodiment, the sidewalls 2435a of the cutout provide clearance for engagement of the cap holder ly 2420 with the receptacle 2433. The bottom wall 2435b of the cutout provides structure and rigidity to the plunger 2440 and prevents over insertion of the cap holder assembly 2420. As with the previous embodiment, the cap holder assembly 2420 can be secured in the receptacle by a friction ﬁt, or other means.

Referring to FIGS. 102-105, another embodiment of the present invention is shown where a al end 2542 of a plunger 2540 comprises a al end wall 2543 having a proximal locking chamber 2547 disposed therein. The proximal locking chamber 2547 comprises a recessed circular chamber having an oblong or oval entrance 2549. The WO 66742 sidewall 2545 could include ribs or gripping surfaces (not shown) to facilitate handling thereof.

The distal end 2524 of the cap holder 2522 comprises a locking protrusion 2588 having a circular stern 2590 and an oblong or oval locking ﬂange 2592 that s the shape of the entrance 2549 of the distal locking chamber 2547. The stem 2590 preferably has a wall ess that matches the proximal end wall 2543 of the plunger 2540. This conﬁguration allows the locking ﬂange 2592 to be aligned with the entrance and inserted into the proximal locking chamber 2547. After the locking ﬂange 2592 is inserted into the proximal lockng chamber 2547, the cap holder assembly 2520 can be rotated (e.g., 90 degrees), as illustrated by Arrow C, such that the locking ﬂange 2592 rotates in the ar proximal locking chamber 2547, to retain the locking ﬂange 2592 in the chamber 2547 such that the locking ﬂange 2592 cannot be pulled therefrom because of the oblong or oval entrance 2549. A friction fit could be provided to prevent accidental rotation/disengagement. In such an arrangement the cap holder assembly 2520 could lock to the r 2540 until it is rotated an additional 90 degrees with respect to the plunger.

Importantly, other locking ﬂanges 2592, entrances 2549, and cutout geometries are contemplated, and they are not limited to solely oblong or oval geometries. Instead, the locking ﬂange 2592 and the entrance 2549 or cutout may be matching asymmetrical s, rectangular, triangular, or any other geometric arrangement. In use, the antiseptic cap 2582 could be d while the cap holder assembly 2520 is attached to the plunger 2540 or the cap holder assembly 2520 can be removed from the plunger 2540 and used separately.

Another embodiment of the present invention is shown in FIGS. 106-108. A sidewall 2662 of a chamber 2660 of a plunger 2640 comprises a locking lever 2664 having a proximal end 2668 and a distal end 2672, and is connected to the sidewall 2662 by a living hinge 2666, which acts as a fulcrum. The proximal end 2668 comprises a locking protrusion 2670 that s a groove in the cap holder 2622 of the cap holder assembly 2620, thus locking it when the cap holder 2622 is secured within the r 2660 of the plunger 2640. By pushing on the distal end 2672 of the g lever 2664, the proximal end 2668 rotates about the living hinge 2666, illustrated by lines D, causing the locking protrusion 2670 to disengage from the groove in the cap holder 2622, thereby ng removal of the cap holder assembly 2620 from the chamber 2660.

Moreover, shown in FIGS. 109 and 110, the distal end 2772 of the locking lever 2764 could have a toe 2773 to facilitate removal of the cap holder assembly 2720 from the chamber 2760 of the plunger 2740. When the distal end 2772 of the locking lever 2764 is d and the proximal protrusion 2770 of the proximal end 2768 s about the living hinge 2766, rated by lines E, and disengages from the cap holder 2722, the toe 2773 pushes against the cap holder assembly 2720 and the shape of the toe 2773 urges the cap holder assembly 2720 out of the r 2760, illustrated by line F. ing to 1, r embodiment of the present invention is shown where a ﬁrst adhesive material 2894a is ﬁxed to the distal end 2824 of a cap holder assembly 2820 and a second adhesive material 2894b is ﬁxed to the proximal end 2842 of the r 2840 of the syringe. The two adhesive materials 2894a, 2894b are removably attachable to one another. The adhesive materials 2894a, 2894b could be any suitable adhesive or could be another type of material that can form a connection, such as hook and loop fasteners where material 2894a could be comprised of hooks, and material 2894b could be comprised of loops. In this way, the cap holder assembly 2820 could be edly attached to the plunger 2840. Further, when the cap assembly 2820 is attached to the plunger 2840, the cap may be removed from the cap assembly 2820, without ﬁrst having to remove the cap holder assembly 2820 from the plunger 2840.

Another embodiment is shown in FIGS. 112 and 113, where a proximal end of the plunger comprises an axially compressible material 2998, such as foam or accordion folded c, deﬁning a cavity. As shown in 2, a cap holder assembly 2920 could be inserted into the cavity, such as by the path illustrated by Arrow G, and secured therein by the frictional radial force of the compressible material 2998 against the outer surface 2926 of the cap holder 2922. As shown in 3, when the compressible material 2998 is compressed, as rated by Arrows H, the cap holder assembly 2920 is easily gripped and removed.

Referring to 4, another embodiment of the present invention is shown. A plunger 3040 could have an annular ﬂange 3067 at a peripheral proximal end 3066 of a chamber 3060 and a cap holder 3022 could have an annular ﬂange 3027. When the cap holder assembly 3020 is fully inserted into the chamber 3060 of the plunger 3040 the two ﬂanges 3027, 3067 are spaced apart by a distance. The spaced distance allows a user to grip the ﬂange 3027 of the cap holder 3022, and thus easily remove the cap holder assembly 3020 from the chamber 3060.

FIGS. 115-118 show another embodiment of the t invention comprising a ly compressible locking ring 3174 attached to a peripheral proximal end 3166 of a plunger 3140. The locking ring comprises press tabs 3178 and diametrically opposed locking tabs 3176. As shown in 6, the distance between the g tabs 3176 is less than the diameter of the cap holder 3122, thus securing the cap holder assembly 3120 in the chamber 3160 of the plunger 3140. When a diametrically opposed force is d at the press points 3178, as shown by Arrows I, the locking ring 3174 s and the locking tabs 3176 separate from each other, shown by Arrows J, sufﬁcient to allow the removal of the cap holder ly 3120 from the chamber 3160 of the plunger 3140. 8 shows another embodiment of the locking ring 3274 sing locking tabs 3276 where the locking ring 3274 is generally circular in shape, and where a force applied, illustrated by lines K, results in the tabs 3276 separating, illustrated by lines L.

From the foregoing, it will be observed that numerous variations and modiﬁcations may be effected without departing from the spirit and scope of the invention. It is to be understood that no limitation with respect to the speciﬁc apparatus illustrated herein is intended or should be inferred. It is, of course, intended to cover by the appended claims all such modiﬁcations as fall within the scope of the claims.

Claims

CLAIMS What is claimed is:

1. An antiseptic cap and syringe combination comprising: a cap holder assembly sing an antiseptic cap disposed in a cap holder and enclosed therein by a cover; and a syringe plunger having a chamber at a proximal end, the chamber defined by a sidewall having a eral proximal end defining an opening, and a distal bottom, and n an interior edge in the sidewall and bottom defines at least one aperture ing access to the chamber.

2. The antiseptic cap and e combination of claim 1, wherein the chamber of the syringe plunger comprises a plurality of circumferentially spaced ribs.

3. The antiseptic cap and e combination of claim 2, wherein the cap holder comprises a bulge in an outer surface of the cap holder, and the ity of circumferentially spaced ribs comprise at least one groove for removably receiving the bulge.

4. The antiseptic cap and syringe ation of claim 3, wherein the plurality of circumferentially spaced ribs further comprise a second groove positioned between the first groove and a proximal end of the chamber.

5. The antiseptic cap and syringe combination of claim 1, wherein the plunger comprises a plurality of support walls extending longitudinally along the plunger, and wherein one or more of the support walls has a recessed area extending longitudinally along a peripheral edge thereof.

6. The ptic cap and syringe combination of claim 1, wherein the r r comprises a first set of support walls at a distal portion of the plunger, and a second set of support walls at a proximal portion of the plunger, the second set of support walls including two walls flanking the aperture in the chamber, the two walls spaced apart by an angle greater than 90 degrees.

7. A method of using an antiseptic cap disposed on a plunger of a syringe having a chamber at a proximal end, comprising: contacting a cap holder of a cap holder assembly, at a bottom surface thereof, through an aperture in the chamber; urging, through the aperture, the cap holder assembly out of the chamber; removing the cap holder assembly from the syringe plunger; and 1001407751 storing the cap holder assembly for use in the future.

8. The method of claim 7, further comprising the step of using the cap holder assembly by removing the cover of the cap holder assembly, and applying the ptic cap to an access site.

9. The method of claim 8, further comprising the step of gripping the cap holder to position the antiseptic cap on the access site, turning the cap holder to thread the antiseptic cap onto the access site, and pulling the cap holder to withdraw the antiseptic cap from the cap .

10. The method of claim 7, wherein the step of urging comprises pushing on the bottom of the cap holder to move a bulge of the cap holder out of a first groove in circumferentially spaced ribs in the chamber of the plunger.

11. The method of claim 10, wherein the ribs have a second groove that receives the bulge of the cap holder as the cap holder assembly progresses out of the chamber, and wherein the step of urging the cap holder assembly out of the chamber further comprises pushing the bulge past the second groove.

12. A method of using an antiseptic cap disposed on a plunger of a syringe having a chamber at a al end, comprising: contacting a cap holder of a cap holder assembly, at a bottom surface thereof, through an re in the chamber; urging, through the aperture, the cap holder ly out of the chamber; removing the cap holder assembly from the syringe plunger; and applying the ptic cap to a l implement.

13. The method of claim 12, further comprising the step of using the cap holder assembly by removing the cover of the cap holder assembly prior to applying the antiseptic cap to the medical implement.

14. The method of claim 13, further comprising the step of ng the cap holder to position the antiseptic cap on the medical implement, turning the cap holder to thread the antiseptic cap onto the medical implement, and pulling the cap holder to withdraw the antiseptic cap from the cap holder.

15. The method of claim 12, wherein the step of urging comprises pushing on the bottom of the cap holder to move a bulge of the cap holder out of a first groove in circumferentially spaced ribs in the chamber of the plunger. 1001407751

16. The method of claim 15, wherein the ribs have a second groove that receives the bulge of the cap holder as the cap holder assembly progresses out of the chamber, and wherein the step of urging the cap holder assembly out of the chamber further comprises pushing the bulge past the second groove.

17. A method of providing an antiseptic cap and e combination, comprising: providing a cap holder assembly comprising an antiseptic cap disposed in a cap holder and enclosed therein by a cover; and ing a syringe plunger having a chamber at a proximal end, the chamber defined by a sidewall having a peripheral proximal end defining an opening, and a distal bottom, and wherein an interior edge in the sidewall and bottom defines at least one aperture providing access to the chamber.

18. The method of claim 17, wherein the chamber of the provided syringe plunger comprises a plurality of circumferentially spaced ribs.

19. The method of claim 18, wherein the provided cap holder comprises a bulge in an outer surface of the cap holder, and the plurality of circumferentially spaced ribs comprise at least one first groove for removably receiving the bulge.

20. The method of claim 19, wherein, in the ed plunger, the plurality of circumferentially spaced ribs r comprise a second groove positioned between the first groove and a proximal end of the chamber.

21. The method of claim 17, wherein the provided syringe plunger comprises a plurality of support walls extending longitudinally along the plunger, and wherein one or more of the support walls has a recessed area ing udinally along a eral edge f.

22. The method of claim 17, wherein the provided syringe plunger further comprises a first set of t walls at a distal portion of the plunger, and a second set of support walls at a proximal portion of the plunger, the second set of support walls including two walls flanking the aperture in the r, the two walls spaced apart by an angle greater than 90 degrees. 1001407751