AU2004284836B2

AU2004284836B2 - Drip tray tablet

Info

Publication number: AU2004284836B2
Application number: AU2004284836A
Authority: AU
Inventors: Steven Kritzler; Alex Sava
Original assignee: Novapharm Research Australia Pty Ltd
Current assignee: Novapharm Research Australia Pty Ltd
Priority date: 2003-10-24
Filing date: 2004-10-20
Publication date: 2010-08-05
Anticipated expiration: 2024-10-20
Also published as: AU2004284836A1

Description

WO 2005/041659 PCT/AU2004/001438 DRIP TRAY TABLET Field of the invention 5 This invention relates to a tablet for use in preventing biofilm growth in a drip tray and drainage tube from said drip tray and to a method of manufacture thereof. The invention extends to include use of the tablet for prevention of biofilm growth, for example in a drip tray. 10 Background of the Invention Drip trays are widely used in industrial and domestic environments where water condenses. For example, in air conditioning systems and the like, it is usual to provide a 15 drip tray under condensation or refrigeration coils. Condensate falling from the coils is collected in a drip tray which is provided with a drain connected to a water waste system or recirculation system. Other situations in which a drip tray is used are commonplace. A problem with drip trays is that biofilm grows on wet surfaces in the tray. 20 Excessive biofilm growth can result in the drain becoming blocked which in turn can cause the tray to overflow, and cause flooding. It has been proposed to treat the water or tray surfaces with biocides to inhibit such growth but such systems have been excessively costly in use. The biocides have 25 been non-oxidizing, and have been provided in tablet form. Since non-oxidising biocides are not wide spectrum, i.e. are not effective against certain genera or strains of biofilm-forming organisms, the efficacy of the biocides is reduced over a period of time. Also the microorganisms present in the environment of the non-oxidising biocide over an extended period give rise to increasing resistance of the microorganism to the biocide. 30 Prior art treatments require the tray to be thoroughly cleaned before use and to date no satisfactory answer to the problem in terms of efficacy, biofilm remediation and bacterial resistance has been found. A further difficulty in many cases relates to the trays not being removable and thus being unable to be cleaned since the clearance -2 between the bottom of the coils and the drip tray is normally too limited to allow clear access. In commercial air conditioning systems, drip trays are usually located in an air 5 treatment plant of the building - an area with restricted access. Often the trays are positioned at a height of up to 5m, requiring use of a ladder, and their servicing is done by highly qualified technicians, i.e. expensive and time-consuming. It is not uncommon to find a tray that is serviced once every 12-24 months, if at all. 10 Any discussion of the prior art throughout the specification should in no way be considered as an admission that such prior art is widely known or forms part of common general knowledge in the field. It is an object of preferred embodiments of the present invention to provide an 15 improved method for controlling biofilm in a drip tray and its drainage line or the like, and to provide a tablet for use in the method, and a method of manufacture of such tablets. It is an object of the present invention to overcome or ameliorate at least one of 20 the disadvantages of the prior art, or to provide a useful alternative. Brief statement of the invention The present inventors have conceived the idea of incorporating an enzyme in a 25 drip tray tablet containing a biocide. This has been found not merely to kill microorganisms, but also to remove biofilm and prevent biofilm drain blockage. According to a first aspect the invention provides a tablet for use in a drip tray, the tablet including: 30 an excipient selected so that the tablet will not fully dissolve in water at ambient temperature for a period of at least one month; at least 500 ppm of a biocide; at least one enzyme; and - 2a enzyme preserving means for maintaining enzyme activity in a moist environment. By "slowly soluble" is meant an excipient such that the tablet will not fully 5 dissolve in water at ambient temperature for a period of at least one month, and preferably, will not fully dissolve for a period of more than 6 months, or even more preferably, will not fully dissolve for a period of more than 12 months. In other preferred embodiments, the tablet will not fully dissolve in water at ambient temperature for a 10 WO 2005/041659 PCT/AU2004/001438 -3 period of 1 to 12 months. In alternate embodiments the period is 1 to 6 months or 6 to 12 months. An example of a suitable excipient is Poly Vinyl Alcohols (PVAs). Other excipients may be selected from high molecular weight polyethyleneglycols, high molecular weight polypropyleneglycols, esters or partial esters of said 5 polyethyleneglycols or polypropyleneglycols, high molecular weight thermoplastic surfactants such as polyoxyethylenecondensates, polyoxypropelene condensates or polyoxyethylenepolyoxypropylene copolymers with appropriate hydrophobes or blends of these and/or other appropriate compounds. 10 The enzyme may be a single enzyme or a combination of enzymes and preferably is selected from proteolytic and/or hydrolase enzymes. Incorporating an enzyme into a drip tray tablet is problematic in practice because in use the tablet in the drip tray becomes saturated with water. This destroys the enzyme 15 activity in the non-dissolved part of the tablet in days or weeks, thus reducing the biofilm destroying properties of the enzymes. According to a second aspect the invention provides a tablet for use in a drip tray including a slowly soluble excipient, a biocide, at least one enzyme, and enzyme 20 preserving means for maintaining enzyme activity in a moist environment wherein the means for preserving the enzyme activity is inclusion in the tablet composition of a boron compound in a concentration sufficient to maintain some enzyme activity for at least three months during use. 25 A preferred boron compound is borax, which the present inventors have found acts to preserve the enzyme activity in use for at least 3 months in the non-dissolved part of the tablet. The present invention thus provides matching between the enzyme activity and tablet dissolution parameters. 30 The invention may preferably contain excipient in an amount of from 2 to 95%, more preferably from 10 to 80%, even more preferably from 20 to 60% by weight of the tablet. The biocide may be preferably be present in an amount of from 0.1 to 20%, more preferably 0.5 to 10%, and most preferably from 1 to 5% by weight of the tablet. The WO 2005/041659 PCT/AU2004/001438 -4 enzyme may preferably be present in an amount of up to 10%, more preferably up to 5% and most preferably up to 3% by weight of the tablet. The inhibitor is preferably present in an amount of from 0.1 to 10%, more preferably 0.2 to 5% and most preferably I to 3% by weight of the tablet. The enzyme preserving means is present in an amount of 5 from 0.1 to 10% by weight of the tablet, preferably in an amount of from 0.1% to 3% by weight of the tablet. According to a third aspect the invention provides a tablet for use in a drip tray including a slowly soluble excipient, a biocide, at least one enzyme, enzyme preserving 10 means for maintaining enzyme activity in a moist environment and a surfactant. According to a fourth aspect the invention provides a tablet for use in a drip tray including a slowly soluble excipient, a biocide, at least one enzyme, enzyme preserving means for maintaining enzyme activity in a moist environment wherein the means for 15 preserving the enzyme activity is inclusion in the tablet composition of a boron compound in a concentration sufficient to maintain some enzyme activity for at least three months during use and a surfactant. For preference tablets according to the invention are made in a tablet press. 20 Alternatively, the tablets may be made by extrusion and cutting, by pouring into moulds, or by providing in a slow release encapsulation. For example, a suitable pressure is applied at ambient temperature to a suitable powdered mixture to prepare a tablet according to the invention. The mixture is pressed 25 into a tablet mould (pretreated with a releasing agent if required) to obtain the tablet. Unless the context clearly requires otherwise, throughout the description and the claims, the words 'comprise', 'comprising', and the like are to be construed in an inclusive sense as opposed to an exclusive or exhaustive sense; that is to say, in the 30 sense of "including, but not limited to".

WO 2005/041659 PCT/AU2004/001438 -5 Preferred embodiments of the invention A preferred embodiment of the invention will now be described by way of example only. 5 Example 1 A tablet according to the invention is formulated as follows; Chemical Name Commercial Cas No Supplier %w/w Name C16-C18 Fatty Alcohol Luhtensol AT50 102-60-3 Langdons 33 Polyethylene Glycol Ether (50EO) Polyvinyl alcohol Gohsenol G105 Nippon Gohsei 40 Sodium sulfate 7757-82-6 APS Chem. 20 Calcium stearate APS Chem 3 2 Bromo-2-nitropropane-1,3-diolBronopol/Canpres Canpoint 2 BNPD Subtilsn-Protease Enzyme Savinase 0.9T 52-51-7 Novozymes 2 Borax Spectrum 1.5 10 The inclusion of a C 16-C18 fatty alcohol or other surfactant is optional and depending on water quality may vary from 0.5 to 50% w/w. Different levels of saponification hydrolysis of Poly Vinyl Alcohol may be employed depending on the desired tablet solubility in cold or hot water. For the lowest solubility tablets higher degrees of saponification hydrolysis (e.g. Gohsenol N-500) should be used, while lower 15 saponification hydrolysis of Poly Vinyl Alcohol (e.g. Gohsenol G105) will result in fast solubilising in cold water. The amount of sodium sulfate may be varied from about 5 to 70%w/w and acts as a densifier. The calcium stearate is an optional solubility modifier and mould release 20 agent. Other biocides may be substituted for the 2 Bromo-2-Nitropropane-1,3 Diol and WO 2005/041659 PCT/AU2004/001438 -6 the concentration may be varied according to the biocide selected and conditions of use. Similarly other enzymes may be substituted for Savinase 0.9T. Boric acid or other suitable compounds may be substituted for borax and at least 5 0.2%w/w will generally be needed. A tablet according to the invention may be manufactured by the following procedure: 10 Example 2 20 -100 atm pressure is applied at ambient temperature to a powdered mixture having a composition according to Example 1 . The mixture is pressed into a tablet mould, pre-treated with a releasing agent if required. 15 A suitable (accelerated) test method is as follows: A tablet to be tested is placed into a 1L plastic tray filled with water. A thin jet of cold (approx 20'C) tap water is introduced in the tray to allow full replacement of 20 water every 10 minutes. The rate of dissolution of the tablet is observed and results are reported every 24 hours. Each 24-hr period of the above test corresponds roughly to 45 days under field conditions. A tablet prepared in accordance with example 2 has a dissolution rate of 94 hours 25 in the above test. When Gohsenol N500 (low cold water solubility) is used instead of Gohsenol Gl 05, the dissolution rate increases to 227 hours in the above test (equivalent to around 15 months in the field). 30 The rate of dissolution of the tablet is preferably maintained at between 4 and 10 days in the above test to correspond to 6-15 months in the field. While it is possible to extend the dissolution rate even further, to do so has been found to compromise biocidal WO 2005/041659 PCT/AU2004/001438 -7 and biofilm removal performance in some cases. Conditions in the field vary and biocide molecules may undergo some changes at extreme temperatures that may be encountered. 5 Comparison with prior art A commercially available drip tray tablet which is composed of surfactants and biocide was inserted into a first metal drip tray with a flexible, transparent PVC tubing drain line that both had visible biofilm. The plant was situated in the locked plant room 10 of an upper floor of a commercial building. The tablet was placed adjacent to the drain line. Over the ensuing six weeks the tablet not only did not remove the biofilm but the biofilm continued to develop to the extent that the drainage line from the drip tray became blocked. With the only available drainage from the tray closed off the water overflowed from the tray causing water damage to the floor below. 15 A second identical drip tray sited immediately adjacent to the first tray into which drained the condensate from an identically sized air conditioning cooling coil was at the same time fitted with a tablet with a composition matching that described in example 1. This tray and drain line also had visible biofilm at the time of tablet addition 20 both adjacent to and in the drain line. When the drip trays were inspected after four weeks this drip tray was found to have no biofilm whatsoever in the immediate vicinity of the tablet and a lessened amount nearby. Most notably the biofilm in the drain line had visibly decrease almost to the point of complete removal. 25 The rate of dissolution of the tablet is largely dependant upon the temperature and humidity. At times of high temperature and humidity the tablet dissolves significantly faster due to the much greater amount of water dripping onto the tablet and may dissolve within four to eight weeks. At the other extreme, if temperatures and humidity are low, a tablet may not dissolve within twenty five to fifty weeks. 30 The rate of dissolution of the tablet can be largely controlled by varying the soluble high molecular weight components of the formulation, i.e. by increasing the molecular weight and the proportion of this slow dissolving component the tablet will WO 2005/041659 PCT/AU2004/001438 -8 last longer. Alternatively the size of the tablet can be increased. However the rate of solution must be sufficiently high to ensure the efficacy of the enzyme and biocide combination contained in the tablet. 5 Formulations and methods of manufacture herein disclosed may be altered to an extent which will be apparent to those skilled in the art from the teaching hereof without departing from the inventive concept herein disclosed.

Claims

1. A tablet for use in a drip tray, the tablet including: an excipient selected so that the tablet will not fully dissolve in water at 5 ambient temperature for a period of at least one month; at least 500 ppm of a biocide; at least one enzyme; and enzyme preserving means for maintaining enzyme activity in a moist environment. 10

2. A tablet according to claim I wherein the excipient is selected such that the tablet will not fully dissolve in water at ambient temperature for a period of at least 6 months.

3. A tablet according to claim 1 wherein the excipient is selected such that the tablet 15 will not fully dissolve in water at ambient temperature for a period of at least 12 months.

4. A tablet according to any one of the preceding claims wherein the excipient includes one or more compounds selected from the group consisting of poly vinyl alcohols, high molecular weight polyethylene glycols, high molecular weight 20 polypropylene glycols, esters or partial esters of polyethylene glycols or of polypropylene glycols, and high molecular weight thermoplastic surfactants.

5. A tablet according to claim 4 wherein the excipient includes one or more high molecular weight thermoplastic surfactants compounds selected from the group 25 consisting of polyoxyethylene condensates, polyoxypropylene condensates, polyoxyethylene-polyoxypropylene copolymers with appropriate hydrophobes, and combinations thereof.

6. A tablet according to any one of the preceding claims wherein the at least one 30 enzyme is selected from the group consisting of proteolytic and hydrolase enzymes.

7. A tablet according to any one of the preceding claims wherein the enzyme preserving means includes a boron compound. - 10

8. A tablet according to claim 7 wherein the boron compound is present in a concentration sufficient to maintain enzyme activity for at least three months during use.

9. A tablet according to any one of the preceding claims wherein the excipient 5 comprises 2% to 95% by weight of the tablet.

10. A tablet according to any one of claims 1 to 9 wherein the excipient comprises 20% to 60% by weight of the tablet. 10

11. A tablet according to any one of the preceding claims wherein the at least one enzyme comprises up to 20% by weight of the tablet.

12. A tablet according to any one of claims I to 11 wherein the at least one enzyme comprises up to 5% by weight of the tablet. 15

13. A tablet according to any one of claims I to 1 wherein the at least one enzyme comprises up to 3% by weight of the tablet.

14. A tablet according to any one of the preceding claims wherein the enzyme 20 preserving means is present in an amount of from 0.1% to 10% by weight of the tablet.

15. A tablet according to any one of the preceding claims wherein the enzyme preserving means is present in an amount of from 0.1% to 3% by weight of the tablet. 25

16. A tablet according to any one of the preceding claims wherein the biocide is present in an amount of from 0.1% to 20% by weight of the tablet.

17. A tablet according to any one of claims 1 to 16 wherein the biocide is present in an amount of from 1% to 5% by weight of the tablet. 30

18. A tablet according to any one of the preceding claims further including a surfactant. - 11

19. A tablet according to any one of the preceding claims when made in a tablet press.

20. A tablet according to any one of the claims I to 18 when made by a process including the step of moulding or the step of extrusion. 5

21. A tablet according to any one of the claims 1 to 18 when provided with slow release encapsulation.

22. A method for inhibiting the growth of a biofilm in a drip tray or the like, including 10 the step of adding to the tray, a tablet according to any one of the preceding claims.

23. A tablet or method substantially as herein described with reference to any one of the examples but excluding any comparatives.