AU2005223917B2 - Biodegradable polyurethane and polyurethane ureas - Google Patents

Description

WO 2005/089778 PCT/AU2005/000436 1 BIODEGRADABLE POLYURETHANE AND POLYURETHANE UREAS FIELD OF THE INVENTION The present invention relates to biodegradable processable and preferably thermoplastic polyurethanes or polyurethane/ureas and processes for their 5 preparation. The polymers are biodegradable, processable and preferably thermoplastic which makes them useful in biomedical applications including, for example, in the fabrication of scaffolds for tissue engineering applications. The invention particularly relates to the use of such polyurethanes and polyurethane/ureas in fabricating scaffolds using rapid prototyping techniques. 10 BACKGROUND TO THE INVENTION Biodegradable synthetic polymers offer a number of advantages over other materials in various biological applications including tissue repair. For example, in relation to the development of scaffolds in tissue engineering, the key advantages include the ability to tailor mechanical properties and degradation 15 kinetics to suit various applications. The simple and routine fabrication of scaffolds with a size and shape similar to organs or parts of organs would, for example, help tissue engineering technology to develop such organs in vivo or in vitro using bioreactors. Likewise, scaffolds with appropriate mechanical properties can be fabricated and implanted in the body to help repair damaged tissues such 20 as those in coronary arteries and other blood vessels. For example, biodegradable scaffolds fabricated as coronary stents can support the vessel during the healing process and degrade and be released from the body after the vessel is repaired. Synthetic polymers are also attractive in tissue engineering applications 25 because they can be fabricated into various shapes with desired pore morphologic features conducive to tissue in-growth. Furthermore, polymers can be designed with chemical functional groups that can, for example, induce tissue in-growth, or be utilised to adapt the polymers to the application in question. A vast majority of biodegradable polymers studied in these fields belong to 30 the polyester family. Among these, poly(a-hydroxy acids) such as poly(glycolic acid), poly(lactic acid) and a range of their copolymers have historically comprised the bulk of published material on biodegradable polyesters and have a long history of use as synthetic biodegradable materials in a number of clinical WO 2005/089778 PCT/AU2005/000436 2 applications. Poly(glycolic acid), poly(lactic acid) and their copolymers, poly-p dioxanone, and copolymers of trimethylene carbonate and glycolide have been the most widely used as scaffolds. Their major applications include as resorbable sutures, drug delivery systems and orthopaedic fixation devices such as pins, 5 rods and screws. Among the families of synthetic polymers, the polyesters have been attractive for these applications because of (i) their ease of degradation by hydrolysis of the ester linkage, (ii) degradation products are resorbed through the metabolic pathways in some cases and (iii) the potential to tailor the structure to alter degradation rates. 10 The recent interest in finding tissue-engineered solutions to repair damaged tissues and organs due to injury/disease has led to the development of new degradable polymers that meet a number of demanding requirements. These requirements range from the ability of the polymer scaffold to provide mechanical support during tissue growth and gradual degradation to 15 biocompatible products, to more demanding requirements such as the ability to incorporate drugs, cells and growth factors, for example, and provide cell conductive and inductive environments as well as promotion of the healing process. Drugs to suppress inflammatory response and promote the healing process can be incorporated within the biodegradable polymer scaffold or as a 20 drug-eluting coating on the surface of the scaffold. Many of the currently available degradable polymers do not meet all of the requirements to be used in such applications. Most biodegradable polymers in the polyester and ester family, for example, are hydrophobic in nature and as such, only a limited number of drugs can be incorporated into such polymers. 25 In particular, biodegradable synthetic polymers with appropriate mechanical properties are sought after for the development of biodegradable stents and stent coatings for the treatment of coronary artery disease by percutaneous intervention. Stents provide mechanical support for the vessel and keep the lumen open to its normal diameter while tissue growth takes place to 30 repair the affected vessel wall. Current stents are fabricated using metals such as stainless steel or nickel-titanium alloys, and once deployed these stents remain permanently within the vessel. Biodegradable polymers have the advantage of being removable from the vessel through polymer degradation and resorption WO 2005/089778 PCT/AU2005/000436 3 once the vessel is repaired. This leaves the repaired vessel free of foreign material and allows re-stenting if needed in the future. Biodegradable polymers can also be useful in delivering drugs such as sirolimus, everolimus and paclitaxel D-actinomycin, all of which help to inhibit the formation of neointimal hyperplasia 5 by suppression of platelet activation, suppression of inflammatory response, and promotion of the healing. Scaffolds made from synthetic and natural polymers, and ceramics have been investigated extensively for orthopaedic repair. The use of scaffolds has advantages such as the ability to generate desired pore structures and the ability 10 to match size, shape and mechanical properties to suit a variety of applications. However, shaping these scaffolds to fit cavities or defects with complicated geometries, to bond to bone tissue, and to incorporate cells, drugs and growth factors, and the requirements of open surgery are a few major disadvantages of the use of known scaffold materials. 15 The most common synthetic polymers used in fabricating scaffolds for growing cells and for biodegradable stents and stent coatings belong to the polyester family. For example, poly(glycolic acid) and poly(lactic acid) have been the most commonly used polymers because of their relative ease of degradation under hydrolytic conditions and the resorption of the degradation products into the 20 body. However, these polymers have a number of disadvantages, including rapid loss of mechanical properties, long degradation times, difficulty in processing, and the acidity of degradation products resulting in tissue necrosis. These polymers, when used in biodegradable stents, have to be heated during the deployment process to temperatures as high as 70'C which can cause cell damage. 25 Common methods that are currently employed for the synthesis of three dimensional biodegradable tissue engineering scaffolds include: porogen leaching, gas foaming, phase separation and the use of non-woven mesh. All of these methods have disadvantages including that: e they require a mould to shape the scaffold - this is costly and can 30 only produce a single shape; * these methods offer little or no control over the orientation of the pores and degree of interconnectivity; WO 2005/089778 PCT/AU2005/000436 4 e usually a polymer skin forms on a moulded scaffold (even if it is porous) which can require extensive post-synthesis treatment; and * some of the methods of scaffold fabrication such as phase separation and porogen leaching often involve the use of toxic 5 organic solvents which is undesirable. A controlled rapid prototyping method can address these problems. The shape of the mould can be quickly altered by computer design, the direction and degree of porosity can be specified to exact levels, a polymer skin is not formed in production, and the process is solvent free. When fabricating scaffolds such as 10 stents for example, the process can be modified to deposit a grid like layout with polymer strands to dimensions and patterns specific to the stent design. The grid structure can then be used to fabricate the stent. Alternatively, the grid structure could be deposited on a rotating mandrel to fabricate the stent in one operation. There are a number of different rapid prototyping machines available in the 15 marketplace. Synthetic polymers that can be used in such rapid prototyping apparatus need to meet specific property requirements which include melt processing characteristics, mechanical properties and other properties. For example, in fused deposition modelling (FDM) applications, the polymer must be able to be 20 melt-processed into a filament of appropriate diameter for the rate of extrusion of the particular FDM apparatus. Most synthetic biodegradable polymers do not meet the requisite property requirements. A review of the literature indicates that among the biodegradable polymers only poly-(E-caprolactone) meets some of the requirements. Hutmacher 25 et al at the National University of Singapore (Biomaterials, 24: 4445-4448, 2003) have reported the use of poly-(E-caprolactone) (PCL) (MW 80,000) to fabricate tissue engineering scaffolds. They have also reported the use of hydroxyapatite as a filler (Schantz et al, Materials Science and Engineering 20: 9-17, 2002) in PCL to fabricate 3D constructs for bone tissue applications. A report by a group 30 from the University of Nottingham (Christian et al, Composites: Part A, 32: 969 976, 2001), discusses PCL impregnated with long glass fibre in a MDM (Material Deposition Modelling) process to fabricate scaffolds. Commercially the market for biodegradable structures with interconnected pores is very large and growing 5 rapidly. One product available is Degrapol* foam which is based on polyurethanes but they have much less control of the degree of porosity, orientation of pores and pore morphology, and it is available only as small foam discs (except on special order). 5 Polymers that can be used to fabricate biodegradable scaffolds using rapid prototyping techniques such as FDM need to meet a set of criteria including that: - the polymer must be thermoplastic; * the polymer must be extrudable; - the filament must be mechanically stiff and have a low melt viscosity 10 (a high Melt Flow Index); and - the polymer must be biodegradable and biocompatible (eg. contain groups that are liable to hydrolyse and have degradation products that are non-toxic). In short, the use of rapid prototyping machines to make porous, highly 15 controlled and interconnected tissue engineering structures requires a complex combination of various techniques including polymer chemistry, polymer processing, rapid prototyping and tissue engineering and, accordingly, is particularly complex. Accordingly, there is a need for biocompatible and biodegradable polymers that can be processed using methods including rapid 20 prototyping as well as thermal and solvent based methods to fabricate scaffolds and coatings for various biomedical applications including tissue engineering. It is thus one object of this invention to develop polymers with properties suited to use in rapid prototyping techniques which will, in turn, enable the fabrication of three dimensional scaffolds with complicated structures for use in tissue growth 25 and repair therapies and technologies, including the fabrication of stents, and coatings for stents useful in drug delivery. SUMMARY OF THE INVENTION To this end, there is provided a biocompatible biodegradable polyurethane or polyurethane/urea comprising isocyanates, polyol and a conventional chain 30 extender and/or a chain extender having a hydrolysable linking group and wherein the chain extender is free of amino or carboxylic functionalities. Preferably the isocyanates are diisocyanates. The polyurethane or polyurethane/urea may also be prepared using only a diisocyanate and a chain extender wherein the WO 2005/089778 PCT/AU2005/000436 6 chain extender in this instance has dual functionality both as a conventional chain extender and as a polyol. Preferably the polyurethanes or polyurethane/ureas are thermoplastic. Preferably the biocompatible, biodegradable polyurethanes or 5 polyurethane/ureas of the invention are of the general formula H H H H N O O y N -'N O O N R1 R R R 0 2 o 3 0 where R, is from the isocyanate, R 2 is from the chain extender and R 3 is from the 10 soft segment polyol. The pronumeral 'n' represents the average number of repeat units in the hard segment. The pronumeral 'p' is proportional to the molecular weight of the polymer and includes both the hard segment repeat units and the soft segment. Throughout this specification, the term "polyol" should be taken to mean a 15 molecule which has at least two or more functional hydroxyl groups that can react with isocyanate groups to form urethane groups. Examples of polyols include but are not limited to diols, triols, and polyols such as macrodiols. Preferably the polyol has a molecular weight of 200-1000, more preferably 200-600, and even more preferably 200-400. The polyol may be terminated by, for example, a 20 hydroxyl, thiol or carboxylic acid group. Isocyanates suitable for preparation of the polyurethanes or polyurethane/ureas of the invention are those which are selected from the group consisting of optionally substituted aliphatic, aromatic and hindered isocyanates. Throughout this specification, the term "chain extender" should be taken to 25 mean a low molecular weight compound having two or more functional groups that are reactive towards isocyanate and having a molecular weight of less than 350. Chain extenders include functional monomers with degradable arms. The chain extender may be employed to introduce easily degradable hard segment components into the polyurethane or polyurethane/urea structure. Incorporating 30 such chain extenders allows preparation of easily degradable polyurethanes with fewer degradation products. For example, polyurethane based on ethyl-lysine WO 2005/089778 PCT/AU2005/000436 7 diisocyanate and glycolic acid based polyol and chain extender degrades to bioresorbable glycolic acid, lysine, ethylene glycol and ethanol. "Degradable arms" according to the invention are any molecular moiety which may be part of the chain extenders and the molecular moiety structure is 5 preferably biocompatible and bioresorbable on in vivo degradation of the biocompatible, biodegradable polyurethanes or polyurethane/ureas. A "hard segment" polymer according to the invention is one which imbues the copolymer with its physical strength which arises from the nature of the chain extender and the isocyanate selected. 10 According to a preferred embodiment of the invention, the hard segment represents 20 to 100% by weight of the polyurethane or polyurethane/urea. Where the hard segment represents 100% by weight, the chain extender has a dual functionality of being both a conventional chain extender and a polyol. Throughout this specification the term "comprises/comprising" when used 15 is taken to specify the presence of stated features, integers, steps or components but does not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof. It has been found that the polyurethanes and polyurethane/ureas according to the invention form porous or non-porous cross-linked or linear 20 polymers which can be used as tissue engineering scaffolds, and may be used in rapid prototyping techniques including FDM. It has also been found that certain of the biodegradable polyurethanes according to the invention exhibit a glass transition between room temperature and 370C. This property can be used to extrude hard materials on FDM apparatus (going in at 200C) which will soften and 25 even become elastomeric in vivo or while growing cells on scaffolds in a bioreactor at physiological temperatures of 370C. This is also a very useful property for soft tissue applications. The polyurethanes and polyurethane/ureas can be sterilized without risk to their physical and chemical characteristics, preferably using gamma radiation to 30 ensure sterility. The polyurethanes and polyurethane/ureas may incorporate biological and inorganic components selected for their ability to aid tissue repair in vivo, or to create certain physical characteristics for rapid prototyping purposes. When WO 2005/089778 PCT/AU2005/000436 8 cured, the polyurethanes and polyurethane/ureas according to the invention form a biodegradable biocompatible scaffold which may be porous and contain interpenetrating polymer networks so as to enable the inclusion of biological and inorganic components. These biological and inorganic components which are 5 preferably selected from the group consisting of cells, progenitor cells, growth factors, other components for supporting cell growth, drugs, calcium phosphate, hydroxyapatite, hyaluronic acid, nanoparticulate tricalcium phosphate and hydroxyapatite type fillers, adhesives including fibrin, collagen and transglutaminase systems, surfactants including siloxane surfactants, silica 10 particles, powdered silica, hollow fibres which may be used to seed cells in the polyurethanes, and other porogens including, for example, gelatin beads. The biological and inorganic components may be present in quantities according to need, especially in the case of the living additives such as cells and progenitor cells. Amounts of up to at least 20% w/w may be acceptable. 15 The invention also provides a biodegradable, biocompatible polymeric scaffold comprising a cured biocompatible, biodegradable polyurethane or polyurethane/urea being the reaction product of isocyanate, polyol and a conventional chain extender and/or a chain extender having a hydrolysable linking group. 20 In the biodegradable, biocompatible polymeric scaffolds according to this aspect of the invention the isocyanates are preferably diisocyanates. The scaffolds may also be prepared using a diisocyanate and a chain extender wherein the chain extender has the dual functionality of a conventional chain extender and a polyol. Preferably the isocyanate is selected from the group 25 consisting of optionally substituted aliphatic, aromatic and hindered isocyanates. The scaffolds may preferably incorporate biological and inorganic components which are desirably selected from the group consisting of cells, progenitor cells, growth factors, other components for supporting cell growth, drugs, calcium phosphate, hydroxyapatite, hyaluronic acid, nanoparticulate 30 tricalcium phosphate and hydroxyapatite type fillers, adhesives including fibrin, collagen and transglutaminase systems, surfactants including siloxane surfactants, silica particles, powdered silica, hollow fibres which may be used to seed cells in the polyurethanes, and other porogens including, for example, WO 2005/089778 PCT/AU2005/000436 9 gelatin beads. The biological and inorganic components may be present in quantities according to need, especially in the case of the living additives such as cells and progenitor cells. Amounts of up to at least 20% w/w may be acceptable. Preferably the cured scaffolds according to this aspect of the invention 5 have a compressive strength in the range of 0.05-100 MPa. The compressive strength of the scaffold will vary according to its porosity and according to the biological components added. Preferably the scaffolds have pores in the size range of 100-500 micron, more preferably 150-300 micron. More preferably the porous scaffolds are seeded with living biological 10 components or drugs selected so as to aid the tissue repair process in the patient being treated. The biological components so selected may be cells, progenitor cells, growth factors and other components for supporting cell growth. Suitable cells may include osteoblasts, chondrocytes, fibroblasts or other precursor cells. Suitable drugs are any which assist in the tissue engineering application of 15 interest. In one preferred embodiment of the invention, the scaffold is a biodegradable stent useful in treatment of coronary heart disease. In another aspect of the invention, the biodegradable biocompatible polyurethanes or polyurethane/ureas of the invention are utilized as stent 20 coatings in the treatment of coronary heart disease. In another aspect of the invention, there is provided a use of polyurethanes and polyurethane/ureas according to the invention in rapid prototyping techniques such as fused deposition modeling. In another aspect of the invention, there is provided a use of polyurethanes 25 and polyurethane/ureas according to the invention in tissue repair or engineering in a patient requiring such treatment the use comprising inserting in said patient a scaffold which is the cured end product of said biocompatible, biodegradable polyurethane or polyurethane/urea according to the invention prepared by rapid prototyping techniques such as, but not limited to, fused deposition modelling. 30 The polyurethane or polyurethane/urea may preferably include additives or drugs to assist for example in the repair of the damaged bone or cartilage such as cells, progenitor cells, growth factors, or other suitable materials or other additives, such as pharmaceuticals for use in drug delivery. Biological additives used may WO 2005/089778 PCT/AU2005/000436 10 preferably include osteoblasts, chondrocytes, fibroblasts, fibrin, collagen, transglutaminase systems and the like. The invention also provides for the use of biocompatible, biodegradable polyurethanes and polyurethane/ureas according to the invention as a tissue 5 engineering scaffold for assistance in tissue engineering applications such as bone and cartilage repair. Other embodiments of the invention will be evident from the following detailed description of various aspects of the invention. BRIEF DESCRIPTION OF THE FIGURES 10 FIGURE 1 shows the SEM of a polyurethane scaffold made according to Example 1. FIGURE 2 shows the SEM of a polyurethane scaffold made according to Example 1 but under higher magnification. FIGURE 3 shows the scaffold of Example 1 and demonstrates stratified design 15 and overlap in the z axis. FIGURE 4 shows the scaffold of Example 1 showing the interconnected pores in a regular section. FIGURE 5 shows the scaffold of Example 1 under light microscopy and demonstrates optical clarity and fusion. 20 FIGURE 6 shows the scaffold of Example 1 under light microscopy and demonstrates the proliferation of primary ovine fibroblast therein. FIGURE 7 shows the scaffold of Example 9 under optical microscopy after 9 weeks cell culture. FIGURE 8 shows the scaffold of Example 9 under scanning electron 25 microscopy and demonstrates confluent cell growth. FIGURE 9 shows the scaffold of Example 9 under scanning electron microscopy and demonstrates confluence and some bridging. FIGURE 10 shows the scaffold of Example 9 under scanning electron microscopy and demonstrates the bridging of a corner of the 30 scaffold by cell growth. FIGURE 11 shows the scaffold of Example 9 under scanning electron microscopy and shows a dose up of unsupported cells demonstrating a fibrous extra-cellular matrix.

WO 2005/089778 PCT/AU2005/000436 11 DETAILED DESCRIPTION OF THE INVENTION The present invention provides polyurethanes and polyurethane/ureas which are particularly suited to rapid prototyping techniques such as fused deposition modelling and therefore have specific characteristics as described in 5 the preamble of this specification. In a preferred form, this invention provides a biocompatible biodegradable polyurethane or polyurethane/urea comprising diisocyanates, polyol of molecular weight 200-600 and a conventional chain extender and/or a chain extender having a hydrolysable linking group. 10 Isocyanates suitable for preparing polyurethanes and polyurethane/ureas according to the invention include but are not limited to the following: o

O

OCN NCO MLDI - lysine diisocyanate methyl ester 15 O O" OCN NCO ELDI - lysine diisocyanate ethyl ester OCN NCO BDI - Butane diisocyanate 20 OCN NCO HDI - hexamethylene diisocyanate OCN C NCO -4H 2 25 H 1 2 MDI - 4,4'-methylene-bis(cyclohexyl isocyanate) WO 2005/089778 PCT/AU2005/000436 12 Polyols or "soft segments" which may be used to prepare the polyurethanes and polyurethane/ureas of the invention are most preferably those having a molecular weight of 200-400. The structure of the polyol in the present invention is preferably: 5 R" -O'R' oO+R R'O~ R'O,g R'"1 0 0 where h and/or k can equal 0 (as is the case of the dimer, eg, h = 0, j = 1 and k 1) or are integers as is j and R" and R~ independently of each other are hydrogen, hydroxy alkyl, aminoalkyl (both primary and secondary) or carboxy alkyl and R 10 and R' cannot be hydrogen, but can be a linear or branched alkyl, alkenyl, aminoalkyl, alkoxy or aryl. The molecular weight of the entire structure is more preferably 120 to 400. Less preferably the molecular weight can be up to 2000 and much less preferably above 2000. Four examples of suitable soft segments are as follows: 15 0 Poly(E-caprolactone) diol, MW 400 (from Example 1): where R is (CH 2 CH 2 ), R' is (CH 2

)

5 , R" and R' are both H, and j = 1 and (h + k) = 2.96 * (Glycolic acid - ethylene glycol) dimer (from Example 8): where R is (CH 2 CH 2 ), R' is (CH 2 ), R" and R"' are both H, j = 1 and (h + k) 1 * Poly(ethylene glycol), MW 400 (from Example 4): h = 0, k = 0, j = -13, R is 20 (CH 2

-CH

2 ), and R" and R"' are both H " Poly(ethylene glycol) bis(3-aminopropyl) terminated (Aldrich): where R is

(CH

2

-CH

2 ), R" and R.' are both -(CH 2

)

3

NH

2 , j = 34 and (h + k) = 0 Either or both of R and R' can contain nonlinear structures, for example where R' = (CH 2

CHCH

3 ) which is lactic acid. However, the R and R' should preferably not 25 contain groups such as OH and NH 2 which are likely to cause crosslinking. Suitable compounds include but are not limited to the following polyester polyols: 0 0 H+ O- R O-- HF'-'~ 13 PGA - Poly-(glycolic acid) diol, where R is typically - (CH 2

CH

2

)

HOh-- 0 R O H PLA - Poly-(lactic acid) diol, where R is typically - (CH 2

CH

2

)

0 0 5 PCL - Poly-(e-caprolactone) diol, where R is typically - (CH 2

CH

2

)

H+O -- kOH PEG - Poly-(ethylene glycol) 10 Examples of other polyols which may act as soft segments include poly-(4 hydroxybutyrate) diol (P4HB diol), poly-(3-hydroxybutyrate) diol (P3HB diol), polypropylene glycol and any copolymers of the aforesaid including PLGA diol, P(LA/CL) diol, P(3HB/4HB) diol. 15 Chain extenders according to the invention are any low molecular weight molecule having two or more functional groups which when reacted with diisocyanates form a urethane or urea linkage. Preferably the chain extender is difunctional and examples of such chain extenders are diols and dithiols. Diols are also relatively non-toxic and can be resorbed or excreted from the body upon 20 degradation and examples include ethylene glycol, diethylene glycol, tetraethylene glycol, 1,3-propane diol, 1,4-butane diol, 1,6-hexane diol, GA-EG dimer, LA-EG dimer, trimers including a combination of LA and/or GA and EG, and oligomeric diols such as dimers and trimers. Incorporated into the hard segment, these 25 WO 2005/089778 PCT/AU2005/000436 14 chain extenders increase degradation. Esters in the hard segment degrade much faster than urethane linkages. The following chain extenders are illustrated: 0 OH HO-,-----'O L-OH 5 A degradable diol chain extender EG-GA diol, MW ~ 120 0 HO,,-------O J T OH

CH

3 A degradable chain extender EG-LA diol, MW ~ 134 0 10 A degradable diol chain extender EG-4HB diol, MW - 148 Preferred polyurethane and polyurethane/ureas prepared according to the invention may utilise PCL diol, PGA diol, PLA diol or PEG diol and HDI/EG as the 15 hard segment. Another preferred polyurethane or polyurethane/urea according to the invention includes a diol of poly(4-hydroxybutyrate) or copolymers therewith to give an improved range of properties and degradation rates. According to the present invention, the monomeric units of the polyurethanes or polyurethane/ureas of the invention are preferably reacted by 20 bulk polymerisation to form a straight-chain poly-(ester-urethane) block copolymer. Catalysts such as titanium butoxide, Tyzor-LA, stannous octoate, ferric acetyl acetonate, magnesium methoxide, zinc octoate, manganese 2-ethyl hexanoate, amine catalyst may, if desired, be used in such polymerisation. The general form of the repeat units in the polymer after polymerisation is: 25 H H H H 1 1 NLRIO R0 N O OyN} 0 2 0 3 0 WO 2005/089778 PCT/AU2005/000436 15 Where R 1 is from the diisocyanate e.g. hexamethylene diisocyanate. R 2 is from a low molecular weight diol chain extender e.g. ethylene glycol. R 3 is from a soft segment diol e.g. PCL diol (MW 400). The pronumeral 'n' represents the average 5 number of repeat units in the hard segment. The pronumeral 'p' is proportional to the molecular weight of the polymer and includes both the hard segment repeat units and the soft segment. In a preferred embodiment of the invention, the hard segment represents 20 to 100% by weight of the polyurethane / polyurethane/urea. More preferably 10 the hard segment represents 60 to 70% by weight. The polyol and chain extender may be the same compound and this corresponds to the embodiment where the hard segment corresponds to 100% by weight of the polyurethane / polyurethane/urea. It has been found that there must be a reasonably high proportion of hard segment for the materials to have adequate properties to 15 extrude through FDM as well as a reasonably high melt flow index. EXAMPLES The following examples are not intended to limit the invention but rather illustrate the nature of the broad invention and its applicability. Example 1 - Preparation of 12TM4 (65% Hard Segment, 35% PCL DIOL 400). 20 Materials: The PCL diol (molecular weight 402.1) from ERA Polymer Pty was dried at 900C for 4 hours under vacuum (0.1 torr). Ethylene glycol (Aldrich) was degassed at 900C under vacuum (0.1 torr) for three hours and HDI (Aldrich) was used as received. A polyurethane composition based on a mixture of PCL diol, EG and HDI was prepared by a one-step bulk polymerisation procedure. 25 Stannous octoate (Aldrich) was kept moisture-free and used as received. A mixture of PCL (25.000 g) and EG (9.696 g) and stannous octoate (0.0714 g) was placed in a 100 ml predried polypropylene beaker, covered with aluminium foil and heated to 700C under nitrogen in a laboratory oven. HDI (36.732 g) was weighed in a separate wet-tared predried polypropylene beaker 30 and added to the PCL/EG/stannous octoate beaker and stirred manually until gelation occurred (90 seconds), at which time the viscous mixture was poured onto a Teflon coated metal tray to cure at 1000C for a period of about 18 hours. The resulting polymer was clear, colourless and tough.

WO 2005/089778 PCT/AU2005/000436 16 A sample of the polymer after curing was compression moulded at 1750C to a 1 mm thick flat sheet for tensile testing. Dumbbells punched from the sheet were tensile tested using an Instron Model 5568 Universal Testing Machine. The mechanical properties of the materials prepared in EXAMPLE 1 were 5 examined and the results are shown in Table 1. Example la - Post-Synthesis Processing The solid polymer sheet was chopped into about 1 cm 3 pieces with clean tin-snips, cooled in liquid nitrogen and ground into a powder using a cryogrinder. The polymer powder was then dried at 1000C under vacuum overnight. The 10 polymer was extruded on a mini-extruder equipped with a 1.7 mm die at 1800C and 40 rpm. The polymer was taken off by a belt conveyor and cooled at ambient temperature in air without water bath. The filament was spooled and kept under nitrogen in a moisture-free environment for at least one week prior to use. The polymer filament was fed though the FDM apparatus and a small 15 lattice was made to show that the material was suitable for FDM. The scaffolds were characterised by light microscopy and SEM and were shown to have very good precision and weld. It has been shown to work with a number of commercially available nozzle diameters. The operating envelope temperature inside the machine was 250C and the 20 heating zone was set at 1680C. SEM micrographs and optical microscopy of FDM scaffolds are shown in Figures 1-6. Example 2 - Preparation of 12TM1 (A softer material than Example 1, 60% HARD SEGMENT, 40% PCL DIOL 400) Materials: The PCL diol (molecular weight 402.1) from ERA Polymer Pty 25 was dried at 900C for 4 hours under vacuum (0.1 torr). Ethylene glycol (Aldrich) was degassed at 900C /0.1 torr for 3 hours and HDI (Aldrich) was used as received. A polyurethane composition based on a mixture of PCL diol, EG and HDI was prepared by a one-step bulk polymerisation procedure. Stannous octoate (Aldrich) was kept moisture-free and used as received. 30 A mixture of PCL (40.0 g) and EG (11.663 g) and stannous octoate (0.100 g) was placed in a 100ml predried polypropylene beaker, covered with aluminium foil and heated to 700C under nitrogen in a laboratory oven. HDI (48.337 g) was WO 2005/089778 PCT/AU2005/000436 17 weighed in a separate wet-tared predried polypropylene beaker, covered and then added to the PCL/EG/stannous octoate beaker and stirred manually until gelation occurred (90 seconds). The viscous mixture was poured onto a Teflon coated metal tray to cure at 700C for a period of about 18 hours. The resulting 5 polymer was clear, colourless and tough. A sample of the polymer after curing was compression moulded at 1700C to a 1 mm thick flat sheet for tensile testing. Dumbbells punched from the sheet were tensile tested using an Instron Model 5568 Universal Testing Machine. The mechanical properties of the materials prepared in EXAMPLE 2 were 10 examined and the results are shown in Table 1. Example 2a - Post-Synthesis Processing The solid polymer sheet was chopped into about 1 cm 3 pieces with clean tin-snips, cooled in liquid nitrogen and ground into powder using a cryogrinder. The polymer powder was then dried at 700C under vacuum overnight. The 15 polymer was extruded on the mini-extruder equipped with a 1.7 mm die at 1750C and 35-40 rpm. The polymer was taken off on a rotating shaft and cooled at ambient temperature in air without water bath. The filament was spooled and kept under nitrogen in a moisture-free environment for at least one week prior to use. 20 The polymer filament was fed though the FDM apparatus and a small lattice was made to show that the material was suitable for FDM. Example 3 - Preparation of 12TM6 (A harder material than Example 1, 70% HARD SEGMENT, 30% PCL DIOL 400) Materials: The PCL diol (molecular weight 402.1) from ERA Polymer Pty 25 was dried at 900C for 4 hours under vacuum (0.1 torr). Ethylene glycol (Aldrich) was degassed at 900C /0.1 torr for 3 hours and HDL (Aldrich) was used as received. A polyurethane composition based on a mixture of PCL diol, EG and HDI was prepared by a one-step bulk polymerisation procedure. Stannous octoate (Aldrich) was kept moisture-free and used as received. 30 A mixture of PCL (21.0 g) and EG (10.840 g) and stannous octoate (0.070 g) was placed in a 100ml predried polypropylene beaker, covered with aluminium foil and heated to 700C under nitrogen in a laboratory oven. HDI (38.160 g) was weighed in a separate predried polypropylene beaker and added to the WO 2005/089778 PCT/AU2005/000436 18 PCL/EG/stannous octoate beaker and stirred until gelation occurred (60 seconds), at which time the viscous mixture was poured onto a Teflon coated metal tray to cure at 1000C for a period of about 18 hours. The resulting polymer was clear, colourless and tough. 5 A sample of the polymer after curing was compression moulded at 1750C to a 1 mm thick flat sheet for tensile testing. Dumbbells punched from the sheet were tensile tested using an Instron Model 5568 Universal Testing Machine. The mechanical properties of the materials prepared in EXAMPLE 3 were examined and the results are shown in Table 1. 10 Example 3a - Post-Synthesis Processing The solid polymer sheet was chopped into about 1 cm 3 pieces with clean tin-snips, cooled in liquid nitrogen and ground into powder using a cryogrinder. The polymer powder was then dried at 700C under vacuum overnight. The polymer was extruded on the mini-extruder equipped with a 1.7 mm die at 1750C 15 and 40 rpm. The polymer was taken off on a rotating shaft and cooled at ambient temperature in air without water bath. The filament was spooled and kept under nitrogen in a moisture-free environment for at least one week prior to use. The polymer filament was fed though the FDM apparatus and a small lattice was made to show that the material was suitable for FDM. 20 Example 4 - Preparation of 14TM12 (Changing the soft segment to PEG DIOL) Materials: The PEG diol (molecular weight 394.7) from Aldrich was dried at 900C for 4 hours under vacuum (0.1 torr). Ethylene glycol (Aldrich) was degassed at 900C /0.1 torr for three hours and HDI (Aldrich) was used as 25 received. A polyurethane composition based on a mixture of PCL diol, EG and HDI was prepared by a one-step bulk polymerisation procedure. Stannous octoate (Aldrich) was kept moisture-free and used as received. A mixture of PEG (20.000 g) and EG (7.715 g) and stannous octoate (0.0571 g) was placed in a 100 ml predried polypropylene beaker, covered with 30 aluminium foil and heated to 700C under nitrogen in a laboratory oven. HDI (29.428 g) was weighed in a separate predried polypropylene beaker, and added to the PEG/EG/stannous octoate beaker and stirred until gelation occurred (150 seconds), when the viscous mixture was poured onto a Teflon coated metal tray WO 2005/089778 PCT/AU2005/000436 19 to cure at 700C for a period of about 18 hours. The resulting polymer was clear, colourless and tough. A sample of the polymer after curing was compression moulded at 1500C to a 1 mm thick flat sheet for tensile testing. Dumbbells punched from the sheet 5 were tensile tested using an Instron Model 4032 Universal Testing Machine. Example 4a - Post-Synthesis Processing The solid polymer sheet was chopped into about 1 cm 3 pieces with clean tin-snips, cooled in liquid nitrogen and ground into powder using a cryogrinder. The polymer powder was then dried at 1000C under vacuum overnight. The 10 polymer was extruded on the mini-extruder equipped with a 1.7 mm die at 1500C and 40 rpm. The polymer was taken off by a belt conveyor and cooled at ambient temperature in air without water bath. The filament was spooled and kept under nitrogen in a moisture-free environment for at least one week prior to use. The polymer filament was fed though the FDM apparatus and a small 15 lattice was made to show that the material was suitable for FDM. The scaffolds were characterised by light microscopy and SEM and were shown to have very good precision and weld. It has been shown to work with a number of commercially available nozzle diameters. The operating envelope temperature inside the machine was 250C and the 20 heating zone was set at 1680C. Example 5 - Preparation of 14TM3-1 (using a different diisocyanate - MLDI) Materials: The PEG diol (molecular weight 394.7) from Aldrich was dried at 900C for 4 hours under vacuum (0.1 torr). Ethylene glycol (Aldrich) was degassed at 900C /0.1 torr for 3 hours. Methyl ester of Lysine diisocyanate MLDI 25 (Kyowa Hakko Kogyo CO. Ltd) was used as received. A polyurethane composition based on a mixture of PCL diol, EG and HDI was prepared by a one step bulk polymerisation procedure. Stannous octoate (Aldrich) was kept moisture-free and used as received. A mixture of PEG (12.814 g) and EG (16.380 g) and stannous octoate 30 (0.0992 g) was placed in a 100 ml predried polypropylene beaker, covered with aluminium foil and heated to 700C under nitrogen in a laboratory oven. MLDI (70.00 g) was measured in a separate predried polypropylene beaker and added WO 2005/089778 PCT/AU2005/000436 20 to the beaker containing mixture of PEG/EG/stannous octoate and stirred until gelation occurred (-300 seconds), at which time the viscous mixture was poured onto a Teflon coated metal tray to cure at 700C for a period of about 18 hours. The resulting polymer was clear, slightly golden in colour and tough. 5 A sample of the polymer after curing was compression moulded at 1750C to a 1 mm thick flat sheet for tensile testing. Example 6 - Preparation of 16TM9 (100% hard segment using MLDI and EG) Materials: The EG (Aldrich) was degassed at 90)C/0.1 torr for three hours. MLDI (Kyowa Hakko Kogyo CO. Ltd) was used as received. A polyurethane 10 composition based on a 1 to 1 ratio of MLDI and EG was prepared by a one-step bulk polymerisation procedure. Stannous octoate (Aldrich) was kept moisture free and used as received. EG (22.000 g) and stannous octoate (0.0972 g) were weighed into a 100 ml predried polypropylene beaker, covered with aluminium foil and heated to 15 700C under nitrogen in a laboratory oven. MLDI (75.214 g) was measured in a separate predried polypropylene beaker, covered with aluminium foil and also heated under nitrogen at 700C before being added to the EG/stannous octoate and stirred until gelation occurred (-700 sec), at which time the viscous mixture was poured onto a Teflon coated metal tray to cure at 700C overnight for a period 20 of about 18 hours. The resulting polymer was clear, golden in colour, very hard and brittle. Example 6a - Post-Synthesis Processing The melt flow index of the material prepared was measured to be 136 g/1 0 min with a 2.16 kg load. 25 Example 7 - Preparation of 12TM19 illustrating shape memory effects (100% hard segment using MLD1 and 2-ethyl-1,3-hexanediol) Materials: The 2-ethyl-1,3-hexanediol (Fluka) was degassed at 900C /0.1 torr for 3 hours. MLDI (Kyowa Hakko Kogyo CO. Ltd) was used as received. A polyurethane composition based on a 1 to 1 ratio of MLDI and 2-ethyl-1,3 30 hexanediol was prepared by a one-step bulk polymerisation procedure. Stannous octoate (Aldrich) was kept moisture free and used as received. 2-ethyl-1,3-hexanediol (8.269 g) and stannous octoate (0.021 g) were weighed into a 100 ml predried polypropylene beaker, covered with aluminium foil WO 2005/089778 PCT/AU2005/000436 21 and heated to 700C under nitrogen in a laboratory oven. MLDI (12.000 g) was measured in a separate predried polypropylene beaker, covered with aluminium foil and also heated under nitrogen at 700C before being added to the 2-ethyl-1,3 hexanediol /stannous octoate and stirred until gelation occurred (-30 min), at 5 which time the viscous mixture was poured onto a Teflon coated metal tray to cure at 700C overnight for a period of about 18 hours. The resulting polymer was clear, golden in colour, very hard and brittle. Example 7a - Post-Synthesis Processing DSC was taken on a Mettler DSC 30 and showed the Tg to be - 3 0*C. 10 When left at room temperature it was hard and brittle but it reversibly softened in the hand and became elastic. Example 8 - Preparation of a hydrolysable chain extender (15TM7, GA-EG diol) 22.19 g of glycolic acid (GA) (Sigma) was heated at 2000C under nitrogen 15 outgassing in a round bottomed flask equipped with a stillhead sidearm and condenser to collect the water runoff. After 18 hours the nitrogen was stopped and vacuum applied (0.1 torr), by which stage the GA had polymerised to a white solid (PGA). Dry ethylene glycol (EG) (Aldrich) (106 g) was added to the PGA in an approximate ratio of 5:1 in order to transesterify the polymer. This was 20 refluxed for a period of 8 hours in total and was followed by GPC until there were three major products: EG, EG-GA and some EG-GA-GA. The EG was removed under vacuum and heat and the resulting chain extender was used to make a polyurethane (16TM7). Example 8a - Preparation of a polyurethane using a hydrolysable chain 25 extender (16TM7 from Example 8) Materials: The 15TM7 (GA-EG diol chain extender) was degassed at 900C /0.1 torr for three hours, as was the PCL diol (MW400). HDI (Aldrich) was used as received. A polyurethane composition based on an 80% hard segment composition was prepared by a one-step bulk polymerisation procedure. 30 Stannous octoate (Aldrich) was kept moisture free and used as received. 15TM7 (30.73 g) and PCL diol (MW402.099) (20.05 g) and stannous octoate (0.100 g) were weighed into a 100 ml predried polypropylene beaker, covered with aluminium foil and heated to 700C under nitrogen in a laboratory WO 2005/089778 PCT/AU2005/000436 22 oven. HDI (49.47 g) was measured in a separate predried polypropylene beaker, covered with aluminium foil and also heated under nitrogen at 70'C before being added to the PCL diol / 15TM7 /stannous octoate mixture and stirred until gelation occurred when the viscous mixture was poured onto a Teflon coated metal tray to 5 cure at 700C overnight for a period of about 18 hours. The resulting polymer was slightly cloudy, hard but flexible. Table 1 - Mechanical properties of some PCL-based polyurethanes with different hard segment percentages Hard segment Y. Mod UTS Shore Code (Wt %) Elong (%) (MPa) (MPa) (D) 12TM1 60 899±189 103±5 41±1 44 12TM4 65 1300±42 112±3 54±5 52 12TM6 70 1537±141 143±7 56±6 57 10 Table 2 - Melt flow index of various materials The Melt Flow Index of various materials according to the present invention was calculated, along with the readily available commercial materials: acrylonitrile butadiene styrene (ABS), polyamide and investment casting wax 15 (ICW). In order to be suitable for FDM, the materials of the present invention preferably should have a MFI which is similar or higher than that of the commercial samples, without significant degradation of the material. Material Temperature ("C) MFI (g/10min), 2.16kg weight ABS 270 8.5 Polyamide 140 75 ICW 73 9.5 14TM3-1 160 7.64 12TM4-6 165 10.43 16TM9 160 136 WO 2005/089778 PCT/AU2005/000436 23 It will be appreciated that the scope of the invention is not limited to the specific examples described herein but extends to the general inventive concepts defined. None of the examples should be considered limiting. Example 9 - cell compatability of sacffolds 5 This example illustrates the cell compatibility of scaffolds fabricated using polymers prepared according to the invention. Polymers were prepared according to the procedure disclosed in Example 1 and 3D scaffolds were fabricated using the procedure described in EXAMPLE 1A. 10 Three dimensional scaffolds similar to those shown in Figures 1 to 3 were seeded with primary ovine fibroblasts explanted from the aortic heart-valve leaflet. The cells were grown in Dulbecco's Modified Eagle's Medium (DMEM) in static culture for a period of nine weeks. The temperature was 37*C and incubator contained 5% C0 2 (g). The DMEM was replaced every five days. At the end of the 15 nine weeks the scaffolds were cross linked using glutaraldehyde and then dehydrated progressively through ethanol and dried. SEM micrographs and optical microscopy of the cell-seeded FDM scaffolds are shown in Figures 7-11. Example 10 20 This example illustrates the preparation of polyurethanes by varying the weight percentage of hard segment, the molecular weight of the soft segment polyol and the type of polyol. The quantities of the diisocyanate, polyol and the chain extender used are summarised in Table 3. The following example illustrates the procedure used in making sample with code TM 1-9 in Table 3. Other materials in 25 the Table were prepared accruing the same one-step polymerisation procedure. Preparation of TM1-9 (50% hard segment, 50% PCL diol 1000). Materials: The PCL diol (molecular weight 1000) from ERA polymer Pty Ltd was dried at 90*C for four hours under vacuum (0.1 torr). Ethylene glycol (Aldrich) was distilled and degassed at 90LC under vacuum (0.1 torr) for three hours. Ethyl 30 LDI was distilled before use. Stannous octoate (Aldrich) was used as received. A polyurethane composition based on a mixture of PCL diol, EG and eLDI was prepared by a one-step bulk polymerisation procedure.

WO 2005/089778 PCT/AU2005/000436 24 A mixture of PCL diol (20.000g) and EG (3.336g) and stannous octoate (0.040g) were placed in a 100ml predried glass beaker, covered with aluminium foil and heated to 70'C under nitrogen in a laboratory oven. ELDI (16.665g) was weighed in a separate wet-tared predried polypropylene beaker and added to the 5 PCL/EG/stannous octoate beaker, covered with aluminium foil and heated to 700C under nitrogen in a laboratory oven. ELDI was then added to the PCUEG/stannous octoate beaker and stirred manually until gelation occurred at which time the viscous mixture was poured onto Teflon coated metal tray to cure at 1000C for a period of about 18 hours. The resulting polymer was clear, 10 colourless and rubbery. The molecular weight of the polymer was determined by gel permeation chromatography and the results reported in Table 3 are relative to polystyrene standards. Table 3. Formulation details of various polyurethanes prepared. Diisocyanate Chain Extenders Soft Segments GPC Results (in THF) Hard PCL PCL PEG Code Segment eLDI HDI EG EG-LA TETEG 1000 2000 1000 Mn Mw PD (%) (g) (g) (g) (g) (g) (g) (g) (g) TM1-11 30 10.778 - 1.222 - 28.000 - - 97,196 1.65 TM1-9 50 16.665 - 3.336- - 20.000 94,673 172,649 1.82 TM1-14 70 22.551 - 5.449 - - 12.000 - 55,398 92,696 1.67 TM1-15 70 18.587 - 9.413 12.000 - 57,847 115,357 1.99 TM1-16 100 25.111 - - 14.889 - - 28,242 51,038 1.81 TM1-22 50 15.305 1.266 3.429 - - 20.000 - 56,742 94,031 1.66 TM1-23 50 13.889 2.584 3.527 - 20.000 - - 39,369 73,452 1.87 TM1-24 50 12.846 - - - 7.154 20.000 - - 53,266 96,737 1.82 TM1-25 70 16.313 - - - 12.000 - - 50,059 89,809 1.79 TM1-27 33.33 11.759 - 1.574 - 13.333 - 13.333 55,398 97,045 1.75 TM1-28 33.33 - 9.410 - 3.923 13.333 - 13.333 47,625 63,464 1.33 TM1-30 50 16.665 - 3.335 - 10.000 - 10.000 43,770 72,845 1.66 TM1-31 50 14.238 - - 5.762 10.000 - 10.000 30,631 50,196 1.64 TM1-29 50 16.178 - 3.822 - - 20.000 - 59,057 101,750 1.72 TM1-32 50 13.397 - 6.603 - - 20.000 36,466 61,103 1.68 15 Abbreviations: eLDI: lysine diisocyanate ethyl ester, HDI: hexamethylene diisocyanate, EG-LA: ethylene glycol-lactic acid ester diol: TETEG: tetraethylene glycol, PCL: polycaprolactone diol, PEG: poly(ethylene glycol), PD: polydispersity. 20 WO 2005/089778 PCT/AU2005/000436 25 Example 11- use as stent coatings This example illustrates that the polymers could be easily dissolved in solvents such as tetrahydrofuran and coated on stainless steel surfaces. The polymers TM1-9, TM1-11, TM1-14, TM1-15 and TM1-16 were 5 dissolved separately in tetrahydrofuran to make 5%, 10% and 20% solutions. The solutions were used to coat stainless steel coupons by dip-coating and by spin coating (Spin coater: Model WS-400B-6NIPP/Lite, Laurell Technologies Corporation). The coatings adhered well to the stainless steel showing their suitability for coating metallic surfaces. These polymers were also soluble in 10 solvents such as chloroform, dichloromethane, dimethyl formamide and dimethyl acetamide. Example 12 The following example illustrates the preparation of strands, fibres and tubes using a reactive extruder (Prism Model) 15 Polyurethanes were produced on a Prism 16mm twin screw extruder of L/D = 26:1 via liquid feed of the diisocyanate, polyester polyol, ethylene glycol and catalyst. Methyl ester Lysine diisocyanate (m-LDI), polycaprolactone diol GMW 426 ( ERA 2043), chain extender ethylene glycol, and catalyst stannous 2 ethyl 20 hexanoate were used as reagents to prepare polyurethanes with hard segment weight percentage of 65 and 95%. The ratio of isocyanate to hydroxyl was kept at 1:1 and the catalyst loading was 0.1 wt%. The throughput rate was ~ 2g/min and the reaction was controlled via extruder screw speed (for mixing control) and via the temperature settings 25 across the 6 individual barrel sections and the dies. Materials based on 95 and 65% hard segment produced good tubes and filaments. A cross-linked polyurethane was produced using this technique by replacing 40 % of the ethylene glycol with trimethylol propane in the 65% hard segment polyurethane formulation.

26 Example 13 - 15RA40: ELDI/PEG/EG/TMP -80% HS: A cross linked polyurethane material was produced following a one-step procedure as described below. A mixture of pre-dried (degassed) macrodiol PEG (2.5g, MW 394.75), Ethylene glycol (18.77g), Trimethylol propane (1.50g, 5 40 mol% of EG) and catalyst Dibutyltin dilaurate (0.1 wt%) were weighed in a polypropylene beaker. The polymer mixture was then degassed at 70*C for about an hour under a vacuum of 1 torr at 700C. ELDI (7.10g) was weighed in a syringe and added to the polyol mixture and stirred rapidly for about 3 minutes and then poured into a Teflon-coated metal pan and pressed under a nominal 10 load of 8 tonn for 2 hours at 1000C followed by further curing in a nitrogen circulating oven 16 hours. The polymer showed maximum tensile stress (34 ±3 MPa), Youngs Modulus (1.0 +0.2 MPa) and elongation at break 156±32 %). Example 14 A mixture of pre-dried (degassed) macrodiol PEG (10.0g, MW 394.75), 15 Ethylene glycol (7.17g) and catalyst Dibutyltin dilaurate (0.1 wt%) was weighed in a polypropylene beaker. The polymer mixture was then degassed at 700C for about an hour under a vacuum of 1 torr at 70*C. ELDI (32.82g) was weighed in a syringe and added to the polyol mixture and stirred rapidly for about 3 minutes and then poured into a Teflon-coated metal pan and pressed under a nominal 20 load of 8 tonne for 2 hours at 1000C followed by further curing in a nitrogen circulating oven 16 hours. GPC showed molecular weight (MP) 112,000 and had maximum tensile stress (10 ±0.5 MPa), Young's Modulus (3.7 +0.4 MPa) and elongation at break 301±6 %). Comprises/comprising and grammatical variations thereof when used in 25 this specification are to be taken to specify the presence of stated features, integers, steps or components or groups thereof, but do not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof. 30

Claims (18)

1. A biocompatible biodegradable processable polyurethane or polyurethane/urea comprising isocyanate, polyol and a conventional chain extender and/or a chain extender having a hydrolysable linking group, wherein 5 the chain extender is free of amino or carboxylic functionalities.

2. A polyurethane or polyurethane/urea according to claim 1 wherein said isocyanate is a diisocyanate, said polyol is of molecular weight 200 - 1000 and said chain extender is a compound having two or more functional groups that are reactive towards said diisocyanate and has a molecular weight of less than 350. 10

3. A biocompatible biodegradable processable polyurethane or polyurethane/urea comprising isocyanates and a chain extender wherein said chain extender has a dual functionality being both a conventional chain extender and a soft segment polyol, and wherein said chain extender is free of amino or carboxylic functionalities. 15

4. A polyurethane or polyurethane/urea according to claim 1 wherein said isocyanate is selected from the group consisting of lysine diisocyanate methyl ester, lysine diisocyanate ethyl ester, butane diisocyanate, hexamethylene diisocyanate and 4,4'-methylene-bis(cyclohexyl isocyanate).

5. A polyurethane or polyurethane/urea according to claims 1 or 2 wherein 20 said polyol is of the formula: R' O.0-R' g--f O RO ]-[R'-Og R'" 0 0 where h and/or k can equal 0 or are integers as is j and R" and R" independently of each other are hydrogen, hydroxy alkyl, aminoalkyl (both primary and secondary) or carboxy alkyl and R and R' cannot be hydrogen, but can be a linear 25 or branched alkyl, alkenyl, aminoalkyl, alkoxy or aryl. 28

6. A polyurethane or polyurethane/urea according to claim 5 wherein said polyol is selected from the group consisting of polyglycolic acid, poly(lactic acid) diol, poly(E - caprolactone) diol and polyethylene glycol.

7. A polyurethane or polyurethane/urea according to claims 1 or 3 wherein 5 said chain extender is selected from the group consisting of ethylene glycol, diethylene glycol, tetraethylene glycol, 1,3-propane diol, 1,4-butane diol, 1,6 hexane diol, GA-EG dimer, LA-EG dimer, trimers including a combination of LA and/or GA and EG, and oligomeric diols.

8. A polyurethane or polyurethane/urea according to claim 1 wherein said 10 isocyanate is selected from the group consisting of lysine diisocyanate, ethyl ester or hexamethylene diisocyanate; said chain extender is selected from the group consisting of ethylene glycol, ethylene glycol - lactic acid diol, or tetraethylene glycol; and said polyol is selected from the group consisting of poly(s - caprolactone) diol and polyethylene glycol. 15

9. A biocompatible biodegradable polymeric scaffold comprising a cured polyurethane or polyurethane /urea according to any one of claims 1 - 8.

10. A polymeric scaffold according to claim 9 which has a compressive strength of 0.05 - 100 MPa.

11. A polymeric scaffold according to claim 9 or 10 which has pores in a size 20 range of 100 - 500 micron.

12. A polymeric scaffold according to claim 9, 10 or 11 which incorporates biological and/or inorganic components selected for their ability to aid tissue repair in vivo or to create physical characteristics for rapid prototyping purposes.

13. A polymeric scaffold according to claim 12 which incorporates drugs. 25

14. A polymeric scaffold according to any one of claims 9 - 13 which is a stent for use in the treatment of coronary heart disease. 29

15. A polyurethane or polyurethane/urea according to claims 1 - 8 which is a stent coating.

16. A use of polyurethanes or polyurethane/ureas according to any one of claims 1 - 8 in rapid prototyping techniques such as fused deposition modelling. 5

17. A use of polyurethanes or polyurethane/ureas according to any of the claims 1 - 8 in tissue repair or engineering in a patient requiring such treatment the use comprising inserting in said patient a scaffold which is the cured end product of said biocompatible, biodegradable polyurethane or polyurethane/urea prepared by rapid prototyping techniques. 10

18. A biocompatible, biodegradable processable polyurethane or poly urethane/urea substantially has hereinbefore described with reference to the Examples. POLYNOVO BIOMATERIALS PTY LIMITED WATERMARK PATENT & TRADE MARK ATTORNEYS P23872AUPC