Polyester urethanes

CA 02426740 2007-01-11

Polyester urethanes

The present invention relates to polyester urethanes comprising a specific component of polypentadecalactone (PDL).

Plastic materials are valuable synthetic polymeric materials which have secured a prominent place in many applications in the art. By varying the different components of polymers attempts are made to achieve optimum properties for the desired applications, in order to respond precisely and selectively to specific demands. A class of in particular interesting products are polyurethanes since these materials may be produced by addition reactions of preformed segments, without producing undesired side products. A known class of polyurethanes are polyurethanes comprising two different polyester components, namely a. polycaprolactone segment and a polyparadioxanone segment. These materials, described in WO-A-99-42528 and WO-A-99-42147, do show shape memory effects, wherein the polycaprolactone segment serves as trigger segment and the polyparadioxanone segment serves as so called hard segment. The use of polyparadioxanone segments however is problematic in some applications since this segment provides the polyester urethanes with a rather rapid biodegradability. Furthermore a lot of the known polyester urethanes do not show the desired mechanical properties, so that the use of novel segments is necessary, in order to meet the ever increasing demands concerning the applications of polymeric materials. Finally polymeric materials should preferable enable the controlled adjustment of desired properties over a broad range, preferably by means of modifications with minor chemical amendments, only.

It is the object of the present invention to provide a novel polymeric material which is able to overcome the drawbacks cited above in connection with the known materials.

This object is achieved with a polyester urethane comprising as essential component, segments of polypentadecalactone.

The most basic form of the present invention may be seen in the use of polypentadecalactone segments in polyester urethanes. The polypentadecalactone segments may be the only polyestersegments in the polyester urelhan or further

CA 02426740 2003-04-16 segments, different from polypentadecalactone may be present In a preferred embodiment the polypentadecalactone segments are employed as hard segments in the polyester urethane, which, in addition to the polypentadecalactone segments, do comprise further polyester segments, preferably polycaprolactone segments, as soft segments. These further segments may be selected among a broad variety of chemically different components which are suitable as soft segment Specific examples which may be named comprise partially crystalline segments, comprising polyester segments, polyether ester segments and polyether segments, such as polycaprolactone segments (PCL), polycaprolactone-co-polytetrahydrofurane segments (PCL-co-pTHF), tetrahydrofurane segments (pTHF), polypropyleneglycoi segments (PPG) and polyethylenegiycol segments (PEG), as well as glassy segments, comprising polyester and copolyester, such as poly-L-lactid-co-glycolide (ran) (PLGA) and poly-DL-lactide (PDL-LA). in particular a combination of polypentadecalactone segments and poiyethyleneglycole segments enables intriguing properties of the resulting material due to the combination of hydrophobic and hydrophilic segments.

The polypentadecalactone segment, contained in the polyester urethane used in accordance with the present invention, is usually introduced into the polyester urethane in the form of a macro diol. This segment may be obtained by ring opening polymerisation from œ-pentadecalactone employing tin catalysis and using ethylene diol as initiator. The ratio of initiator to monomer controls the molecular weight of the segment. The molecular weight of the polypentadecalactone segments in the polyester urethane used in accordance with the present invention is not critical. Usually the number average of the molecular weight is however in the range of from 1000 to 20,000 g/mol, preferably to 2000 to 11,000 g/mol, determined by GPCanalysis. The macrodiol from pentadecalactone may be converted to a polyester urethane using those diisocyanates which are typically employed for the preparation of polyurethanes. Preferred diisocyanate are compounds having the formula O=C=N-R-N=C=O wherein R is aromatic or aliphatic. Preferably however R is aliphatic comprising a carbon chain of from 1 to 10, preferably 2 to 8 and in particular preferably 4 to 7 carbon atoms. This carbon chain may be saturated with hydrogen of may show additional substituents. These substituents comprise short chain alkyl groups, in particular methyl groups. A preferred diisocyanate is trimethyl hexane-1,6diisocyanate.

CA 02426740 2003-04-16

By varying the molecular weight of the polypentadecalactone segment the properties of the polyester urethane may be varied. The molecular weight of the polyester urethane is not critical and may be selected in accordance with the desired use. Typical molecular weights (number average, determined by GPC) are in the range of from 60,000 to 250,000 g/mol, preferably within the range of 60,000 to 200,000 g/mol and in particular within tiie range of 62,000 to 196,000 g/mol.

The polyester urethanes in accordance with the present invention which comprise polypentadecalactone segments do show a melting temperature, depending from the molecular weight within the range of about 90°C (preferably 87 _ 95°C). Typical mechanical properties are sche E-Modulus of about 17 MPa, an elongation at break at 70 °C of about 1000% and a tensile strength of about 18 MPa. Polyester urethanes comprising polycaprolactone segments, which are known from the prior art do show values for E-Modulus and tensile strength of only 0,5 and 2 MPa, respectively. The material in accordance with the present invention, although differing with respect to their chemical composition only to a minor extend from the polycaprolactone urethanes, are therefore valuable materials having a great potential for a variety of applications. The slower biodegradability of polypentadecalactone segments, compared with polycaprolactone segments enables the application in fields where an increased stability within a physiological environment is desired, for example implants for long time application. The use of segments made from pentadecaiactone further offers the advantage that this monomer is readily available at moderate costs due ta its use within the cosmetic industry.

Preferably the polyester urethane comprises in addition to the polypentadecalactone segment at least one further polyester segment, such as those named above. In particular this further segment is a polycaprolactone segment. These polyester urethanes are block copolymers comprising polypentadecalactone segments, linked with other polyester segments, preferably polycaprolactone segments. The further segments, in particular the polycaprolactone segments, may, as described above for toe polypentadecalactone segment, be introduced into toe polyester urethane in the form of a macrodiol. This macrodiol may be prepared using toe usual processes known to toe skilled person, such as ring opening polymerisation of ε-caprolactone, in accordance with the process described above.

CA 02426740 2003-04-16

The molecular weight of the additional segments, as described above for the polycaprolactone segments, is not critical. However, typically these segments do show a number average of the molecular weight, determined by GPC, of from 1000 to 20.000 g/mol preferably 2,000 to 11.000 g/mol, wherein the preferred range for the PEG segments is from 2000 to 20,000 g/mol, for the PLGA segments from 4000 to 9000 g/mol and for P-DL-LA from 5000 to 11,000 g/mol. The polyester urethanes comprising additional segments, preferably polycaprolactone segments do show preferably a molecular weight of from 50,000 to 250,000 g/mol (number average, determined by GPC), more preferably of from 60,000 to 200,000 g/moi and in particular preferably from 62000 to 196,000 g/mol (and in some embodiments of from 55,000 to 100,000 g/mol). The content of polypentadecalactone units may be varied over a broad range, preferably the content of pentadecalactone units is in the range of from 10 to 80 wt%, in particularly within the range of from 20 to 60 wt%.

When the above described polyester segments are converted by a polyaddition rection using the above disclosed diisocyanates to polyester urethanes in accordance with the present invention, a variation of toe respective amounts and molecular weights of the polyester segments enables an adjustment of toe profile of properties of the resulting polyester urethanes. This preferred embodiment of the present invention provides a polymeric system which enables, by modifying simple starting materials, a.control of the resulting properties.

The materials in accordance with toe present invention may be used in the form of fibres, such as in wrinkle resistant textiles, in the form of different shaped articles, for example in toe field of medicine, as slowly degrading implants or in toe form of coatings, for example on short term implants, such as cannulae or lead-wires. The use as coating material may increase toe bio compatabiiity of toe coated articles and may therefore protect the user from undesired side reactions during use of the coated articles.

The preferred polyester urethanes of the present invention, which comprise in addition to the polypentadecalactone segments further segments, preferably polycaprolatone segments, do display further preferred profiles of properties.

The introduction of further segments, preferably polycaprolactone segments, into the polyester urethanes of toe present invention introduces a second melting temperature,

CA 02426740 2003-04-16 which may be detected during DSC measurements, into the polyester urethane. This second melting temperature usually lies in the range of above 5O^eC, depending from the molecular weight and the proportion of the further segment, preferably the polycaprolactone segment, in the polyester urethane.

In addition the mechanical properties may be controlled over a broad range. With increasing content of polypentadeclactone the value for E-Modulus may be increased as well. The value for the elongation at break may be adjusted to 600 to 1200% with increasing content of polypentadecalactone and in addition tensile strength may be adjusted in a range of from 4 to 10 MPa with increasing content of the polypentadecalactone segment (all values determined at 70’C). The reduced, i.e. slower biodegradability of the polypentadecalactone segments, compared to polyparadioxanone segments used so far in the prior art, the preferred polyester urethanes of the present invention may also be employed in applications for which the known polyester urethanes were not suitable due to their faster degradability and the therewith associated decreased mechanical stability. Compared with known polyester urethanes comprising polycaprolactone segments and polyparadioxanone segments, the polyester urethanes of the present invention furthermore do display an improved production stability and ability to be granulated, which simplifies the production and the processing of the polyester urethanes of the present invention. The known polyester urethanes having poly-p-dioxanone segments in particular undergo degradation reactions upon extrusion, while the polyester urethanes of the present invention do show an improved stability in this respect The materials of the present invention do show a good biocompatability, which was proven with appropriate evaluations.

The more preferred polyester urethanes of the present invention which do comprise polypentadecalactone segments as well as further segments, preferably polycaprolactone segements furthermore do display shape memory properties, so that accordingly these preferred materials may be designated shape memory polymers (SMP).

Such materials are obtained in particular if, within the polyester urethane of the present invention, the polypentadecalactone segments and the further segments, preferably polycaprolactone segments, are present in specified amounts. These specified amounts may be adjusted by appropriate selection of the molecular weight and content (wt.-%) of the further segments, preferably caprolactone segments, and the pentadecalactone

CA 02426740 2003-04-16 segments. Generally speaking, with similar or equal number average molecular weights, SMP materials may be preferably obtained if the content of further segments, preferably caprolactone segments, within the polyester urethane is higher than the content of pentadecalactone units. Is the molecular weight of the further segments, preferably polycaprolaetone segments, within the polyester urethane however higher than the molecular weight of the polypentadecaiactone units, the content of pentadecalactone units may be higher than the content of further segments, preferably caprolactone units.

Good SMP-materials may in particular be obtained using the following compositions:

Polypentadecaiactone segment: Molecular weight 1000 to 10,000 g/mol (number average), preferably 1500 to 5000, in particular 2000 to 3000 g/mol.

Polycaprolaetone segment Molecular weight 3000 to 11,000 g/mol (number average), preferably 4000 to 10,000 g/mol. .

Polycaproiactone-co-polytetranadrbfurane segment: molecular weight 1000 to 5000 g/mol (number average), preferably 1500 to 3500 g/mol.

Polytetrahydrofurane segment: Molecular weight 1000 to 5000 g/mol (number average), preferably 1500 to 3000 g/mol.

Polypropyleneglacol segment: molecular weight 1000 to 8000 g/mol (number average), preferably 1200 to 4500 g/mol.

Polyethyleneglycol segments: Molecular weight 1000 to 25,000 g/mol (number average), preferably 1500 to 20,0000 g/mol.

Poly-L-lactide-co-glycolide segment (ran): Molecular weight 4000 to 10,000 g/mol (number average), preferably 5000 to 8000 g/mol.

Poly-DL-lactide segment: Molecular weight 4000 to 15,000 g/mol (number average), preferably 5000 to 11,000 g/mol.

Polyesterurethane: Molecular weight 50.000 to 200,000 g/mol (number average), preferably 60,000 to 190,000 g/mol; content of the additional segment 20 to 80 wt%,

CA 02426740 2003-04-16 preferably 45 o 70 wt%, more preferably 50 to 60 wt%, content polypentadecalactone segment 80 to 20 wt%, preferably 55 to 30 wt%, more preferably 40 to 50 wt%.

The polymers of the present Invention may be blended with further components, which further widens their range of application. Fillers, such as silica, barium sulfate and similar materials, medicinal active compounds, such as anti bactericides, fünguzides and similar materials of organic or inorganic nature, such as nano-silver, and colorants may be blended with the polymers of the present invention. The valuable properties of the polymers are usually not affected if the addition amount is within the range up to 25% (based on the weight of the total blend), preferably within the range of from 1 to 10%.

it is furthermore possible to blend the polymers of the present invention with other commercially available polymers, such as polyolefins, in particular polyethylene and polypropylene, or vinyl polymers, such as polystyrene and PVC. It could be shown that with an content of from 50 to 90 wt-% of the polymer in accordance with the present invention, the shape memory properties could be retained. This enables in particular tile preparation of low cost SNIP materials since the commercially available blend components are, compared with the polymers of the present invention, relatively cheap and may be blended in an amount of up to 50 wt.-%.

The blending of the above named additional components may be accomplished in a usual manner known to the skilled person, for example by compounding using suitable kneaders or extruders.

The polyester urethanes of the present invention which comprise only pentadecalactone units in the polyester segments furthermore show the surprising property that these polyester urethanes, blended with other polyesters, preferably PCL and a polyester urethane based on PCL yield a biend showing shape memory properties, although the single blend components do not show such properties, The blend ratio preferably is selected in such a way, so that the polyester urethane of the pentadecalactone segments Is present in the blend in an amount of from 20 to 80 wt-%, preferably 40 to 60 wt-%. Without being bound to this theory it is assumed that a compatabillsation is achieved through the urethane segments which yields a mixture, which corresponds, as far as macroscopic properties are concerned, to the covalently crosslinked shape memory materials.

CA 02426740 2003-04-16

Such blends may be prepared by coprecipitation from a solution or by compounding.

Coprecipitation results in a superior mixing. However coprecipitation has drawbacks due to the use of solvents, in particular regarding costs as well as regarding working safety.

The materials in accordance with the present invention furthermore may be processed in order to obtain interesting products, such as foams (porous structures) as weli as micro canters (micro beads), which may be employed over a broad range of applications. Due to the properties of the materials valuable products in particular in the medicinal field may be obtained.

Production of a foam may be carried out in the usual way, such as compounding with a foaming agent and extruding or by thermally induced phase separation of a polymer solution. The type of foaming agent is not critical and it has been proven that usual foaming agents may be employed using master batch technology.

The foams which may be obtained generate, due to their shape memory properties which are not lost due to foam preparation, controlled forces upon recovery of the permanent shape, which opens up further application fields.

During the production of the foam the pore size as well as the pore size distribution may be controlled in the manner known to the skilled person, by adjusting the geometric configuration of the screw, processing temperature and torque

The micro carriers of the present invention, which may for example be employed for Tissue Engineering, may be produced from the materials of the present invention using usual processes, such as solvent evaporation of an emulsion or by thermally induced phase separation of a solution, in each case comprising at least one polyester urethane of the present invention. The size of the micro earners (av. Diameter) may vary within the range of from 100 nm to 800 pm, preferably 100 to 200 pm, depending from the desired field of application. The particles substantially show a spherical shape and often do show an inner hollow cavity. The surface is predominantly smooth with some structures within the nanometer region.

The present invention is further illustrated with the following examples.

Preparation of polyester macrodiols

CA 02426740 2003-04-16

Caprolactone and pentadecalactone, respectively were polymerised under ring opening using ethylene glycol as initiator and dibutyl tin as catalyst, without addition of any solvent, at 13O°C. The typical reaction time was 5 hours. Selecting the amount of initiator adjusts the molecular weight

I in this manner different macrodiols were prepared having molecular weights (number average) of 10000, 2000 and 3000 g/mol for macrodiols form pentadecalactone and 10000 and 4000 g/mol for makrodiols from caprolactone.

Further polyester urethanes, in which the segments of PCL had molecular weights of 2000, 3000, 4000 and 10000 g/mol and in which the segments of PDL has molecular weights of 2000 and 3000 g/mol were evaluated and it was found that the materials showed a melting point of the PCL segments in the range of from 30 to 55'C, which is preferred in particuiar for many applications in the medicinal field.

Preparation of polyester urethanes

These macrodiols were reacted using a mixture .of 2,2,4- and 2»4,4-frimethylbexane-l ,6diisocyanate to obtain polyester urethanes. This reaction was carried out at 80”C using dioctyl tin as catalyst and 1,2-dichloroethyne as solvent. The average reaction time was two days.

In this manner different polyester urethanes were prepared which are summarized in the following table. PDL describes the amount of pentydecalactone within the polyester urethane (neglecting the diisocyanate linkers) as well as the molecular weight of the polypentadecalactone segments. PCL provides the corresponding values for the caprolactone units. The materials of examples 6, 7 and 8 do show pronounced shape memory properties. It should be noted in this connection that the elongation at break, for the materials exemplified here, increases with increasing PDL content of from 700 to 1200%. This clearly demonstrates the influence, concerning the mechanical properties, exerted by toe type of composition. Generally speaking these illustrative examples show that toe present invention provides a polymeric system enabling the controlled adjustment of desired properties.

CA 02426740 2003-04-16

<td> Example</td><td> PDL</td><td> PCL</td><td> Molecular weight of the polyester urethane</td><td> E-Module (70°C I MPa)</td><td> Tensile strength (MPa)</td>

<td> 1</td><td> 100 wt-% / 10000 g/mol</td><td></td><td> Mn= 192000</td><td> 17</td><td> 18</td>

<td> 2</td><td> 22 wt.-% ! 10000 g/mo!</td><td> 78 wt.-% / 10000 g/mol</td><td> Mn- 120000</td><td> 1,4</td><td> 5</td>

<td> 3</td><td> 41 wt.-% / 1OOOO g/mol</td><td> 59 wt-% / 10000 g/mol</td><td> Mn =196000</td><td> 3</td><td> 10</td>

<td> 4</td><td> 60 wt.-% / 10000 g/mol</td><td> 40 wt-% / 10000 g/mol</td><td> Mn =176000</td><td> 7</td><td> e</td>

<td> 5</td><td> 80 wt-% / 10000 g/mol</td><td> 20 wt-% / 10000 g/mol</td><td> Mn =185000</td><td> 8,5</td><td> 7</td>

<td> 6</td><td> 40 wt-% / 2000 g/mol</td><td> 60 wt.-% / 4000 g/mol</td><td> Mn = 86000</td><td> 3,5 35 (RT)</td><td> 4,5 23 (RT)</td>

<td> 7</td><td> 50 wt-% / 3000 g/mol</td><td> 50 wt-% I 10000 g/mol</td><td> Mn = 75000</td><td> 1.5 70 (RT)</td><td> 1.6 24 (RT)</td>

<td> 8</td><td> 40 wt-% / 3000 g/mol</td><td> 60 wt-% / 10000 g/mol</td><td> Mn = 62000</td><td> 3 45 (RT)</td><td> 9 30 (RT)</td>

In order to evaluate the temperature dependence of the mechanical properties experiments were conducted with the material of example 8. The results of these experiments are given in the following table and demonstrate that the tensile stretch remains almost without change even when heating the material to a temperature close to the melting temperature of the polypentadecalactone segments while E-modulus and tensile strength decrease. Comparable polyester urethanes comprising polyparadioxanone segments in place of th epolypentadecalactone segments do show a significantly lower tensile stretch.

CA 02426740 2003-04-16

<td> o -</td><td> Tensile stretch (%)</td><td> E-Modulus (Mpa)</td><td> Tensile strength (MPa)</td>

<td> 22</td><td> 900</td><td> 45</td><td> 30</td>

<td> 37</td><td> 1000</td><td> 25</td><td> 30</td>

<td> 50</td><td> 1000 Ί</td><td> 12 ^H</td><td> 20</td>

<td> 55</td><td> 1050</td><td> 7</td><td> 15</td>

<td> 60</td><td> 1050</td><td> 3</td><td> 10</td>

<td> 65</td><td> 1000</td><td> 3</td><td> 10</td>

<td> 70</td><td> 1000</td><td> 3</td><td> 9</td>

<td> 75</td><td> 1000</td><td> 3</td><td> 7</td>

<td> 80</td><td> 1000</td><td> 1.5</td><td> 3</td>

Furthermore the material was subjected to experiments for the determination of the shape memory properties. Thermo-cyclic experiments were carried out (for an explanation of such experiments see for example the International Patent Applications described in the introductory part of the present application). Values for shape fixity (Rf) and shape recovery after the coursa of several cycles (Rr) were determined. The results are shown in the following table.

<td> Number of cycles</td><td> Rf(%)</td><td> Rr(%)</td>

<td> 1</td><td> 98</td><td> -</td>

<td> 2</td><td> 98</td><td> 85</td>

<td> 3</td><td> 98</td><td> 98</td>

<td> 4</td><td> 98</td><td> 99</td>

<td> 5</td><td> 98</td><td> 99</td>

The above shown experiments were conducted in such a manner that the shape memory effect was initiated at a temperature of 80*C. Similar results may be obtained if the shape memory effect is initiated at temperatures within the range of from 60 to 90’C.

CA 02426740 2003-04-16

In addition the following copolyester urethanes were produced and several mechanical properties were tested.

PDL-fiOfynttane comprising partially crystalline soft segments

Composition of polyester urethane comprising PDL

PDL= polypentadecadolactone, polyester + PCL = polycaproiactone, polyester + PCL-co-pTHF = polycaprolactone-co-polytetrahydrofuran , polyetherester + pTHF= polytetrahydrofuran, poiyether + PPG= polypropyleneglycol, polyether + PEG= Polyethyleneglycol, polyether ( novel combination hydrophobic (PPDL) hydrophilic (PEG)

Combination with PPL 3000 g/mol

<td> Material</td><td> %</td><td></td><td> %</td><td> Mn</td>

<td> PDL 3000 g/mol</td><td> 100</td><td></td><td></td><td> 69.000</td>

<td> PDL 3000 g/mol</td><td> 50</td><td> PCL 1000 g/mol</td><td> 50</td><td> 72.000</td>

<td> PDL 3000 g/mol</td><td> 50</td><td> PCL 1250 g/mol</td><td> 50</td><td> 105.000</td>

<td> PDL 3000 g/mol</td><td> 50</td><td> PCL 2000 g/mol</td><td> 50</td><td> 83.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PCL 2000 g/mol</td><td> 60</td><td> 76.000</td>

<td> PDL 3000 g/mol</td><td> 50</td><td> PCL 3000 g/mol</td><td> 50</td><td> 75.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PCL 3000 g/mol</td><td> 60</td><td> 89.000</td>

<td> PDL 3000 g/mol</td><td> 50</td><td> PCL 4000 g/mol</td><td> 50</td><td> 85.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PCL 4000 g/mol</td><td> 60</td><td> 95.000</td>

<td> PDL 3000 g/mol</td><td> 50</td><td> PCL 10000 g/mol</td><td> 50</td><td> 87.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PCL 10000 g/moi</td><td> 60</td><td> 103.000</td>

<td> PDL 3000 g/mol</td><td> 30</td><td> PCL 10000 g/mol</td><td> 70</td><td> 89.000</td>

<td> PDL 3000 g/mol</td><td> 60</td><td> PCL 10000 g/moi</td><td> 40</td><td> 73.000</td>

<td> PDL 3000 g/moi</td><td> 40</td><td> PCL-co-pTHF 2000g/mol</td><td> 60</td><td> 79.000</td>

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<td> PDL 3000 g/mol</td><td> 40</td><td> PTHF 2500 g/mol</td><td> 60</td><td> 45.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PPG 1200 g/mol</td><td> 60</td><td> 65.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PPG 4000 g/mol</td><td> 30</td><td> 53.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PEG 2000 g/rnol</td><td> 60</td><td> 28.000</td>

<td> PDL 3000 g/mol</td><td> 40 Ί</td><td> PEG 4000 g/mol</td><td> 60</td><td> 32.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PEG 6000 g/mol</td><td> 60</td><td> 40.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PEG 8000 g/mol</td><td> 60</td><td> 42.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PEG 10000 g/mol</td><td> 60</td><td> 43.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PEG 20000 g/mol</td><td> 60</td><td> 50.000</td>

Combination with PPL 2000 o/mol

<td> Material</td><td> %</td><td></td><td> %</td><td> Mn</td>

<td> PDL 2000 g/mol</td><td> 30</td><td> PCL 2000 g/mol</td><td> 70</td><td> 75.000</td>

<td> pdl 2000 g/mol</td><td> 40</td><td> PCL 2000 g/mol</td><td> 60</td><td> 95.000</td>

<td> PDL 2000 g/mol</td><td> 50</td><td> PCL 2000 g/mol</td><td> 50</td><td> 65.000</td>

<td> PDL 2000 g/moi</td><td> 60</td><td> PCL 2000 g/moi</td><td> 40</td><td> 73.000</td>

<td> PDL 2000 g/mol</td><td> 70</td><td> PCL 2000 g/mol</td><td> 30</td><td> 46.000</td>

<td> PDL 2000 g/mol</td><td> 30</td><td> PCL 3000 g/mol</td><td> 70</td><td> 99.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PCL 3000 g/mol</td><td> 60</td><td> 72.000</td>

<td> PDL 2000 g/mol</td><td> 50</td><td> PCL 3000 g/mol</td><td> 50</td><td> 78.000</td>

<td> PDL 2000 g/mol</td><td> 60</td><td> PCL 3000 g/mol</td><td> 40</td><td> 73.000 .</td>

<td> PDL 2000 g/mol</td><td> 70</td><td> PCL 3000 g/mol</td><td> 30</td><td> 65.000</td>

<td> PDL 2000 g/mol</td><td> 30</td><td> PCL 4000 g/mol</td><td> 70</td><td> 49.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PCL 4000 g/mol</td><td> 60</td><td> 62-000</td>

<td> PDL 2000 g/mol</td><td> 50</td><td> PCL 4000 g/mol</td><td> 50</td><td> 85.000</td>

<td> PDL 2000 g/mol</td><td> 60</td><td> PCL 4000 g/mol</td><td> 40</td><td> 83.000</td>

<td> PDL 2000 g/mol</td><td> 70</td><td> PCL 4000 g/mol</td><td> 30</td><td> 56.000</td>

<td> PDL 2000 g/mol</td><td> 30</td><td> PCL 10000 g/mol</td><td> 70</td><td> 85.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PCL 10000 g/mol</td><td> 60</td><td> 109.000</td>

<td> PDL 2000 g/mol</td><td> 50</td><td> PCL 10000 g/mol</td><td> 50</td><td> 130.000</td>

<td> PDL 2000 g/mol</td><td> 60</td><td> PCL 10000 g/mol</td><td> 40</td><td> 121-000</td>

<td> PDL 2000 g/mol</td><td> 70</td><td> PCL 10000 g/moi</td><td> 30</td><td> 91.000</td>

<td> PDL 2000 g/mol</td><td> 30</td><td> PCL-co-pTHF 2000g/mol</td><td> 70</td><td> 6Q.OOO</td>

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<td> PDL 2000 g/mol</td><td> 40 T</td><td> PCL-co-pTHF 2000g/mol</td><td> 60</td><td> 78.000</td>

<td> pdl 2000 g/mol</td><td> 50</td><td> PCL-co-pTHF 2000g/mol</td><td> 50</td><td> 89.000</td>

<td> PDL 2000 g/mol</td><td> 60</td><td> PCL-co-pTHF 2000g/mol</td><td> 40</td><td> 59.000</td>

<td> PDL 2000 g/mol</td><td> 70</td><td> PCL-CO-pTHF 2000g/mol</td><td> 30</td><td> 55.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PPG 1200 g/mol</td><td> 60</td><td> 65.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PPG 4000 g/mol</td><td> 60</td><td> 53.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PEG 2000 g/mol</td><td> 60</td><td> 28.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PEG 4000 g/mol</td><td> 60</td><td> 32.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> PEG 6000 g/moi</td><td> 60</td><td> 40.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PEG 8000 g/mol</td><td> 60</td><td> 42.000</td>

<td> PDL 3000 g/mol ~</td><td> 40</td><td> PEG 10000 g/mol</td><td> 60</td><td> 43.000</td>

<td> PDL 3000 g/moi</td><td> 40</td><td> PEG 20000 g/mol</td><td> 60</td><td> 50.000</td>

Mechanical properties:

<td> Material</td><td> Temp.</td><td> E-Modulus</td><td> Tensile stretch</td>

<td> PDL-2k-co-PCL1 Ok 40/60</td><td> 20°C</td><td> 35</td><td> 1350 %</td>

<td> PDL-2k-co-PCL1 Ok 40/60</td><td> 70^eC</td><td> 5</td><td> 1000%</td>

<td> PDL-3k-co-PCL1 Ok 40/60</td><td> 20°C</td><td> 145</td><td> 1500 %</td>

PDL-paiyurethane comprising glassy components

Composition of polyester urethanes with PDL

PDL= polypentad^cadolacton, polyester

PLGA= poly-L-lactide-co-glycolide (ran), polyester P-DL-LA = poly-D L-lactide, polyester

CA 02426740 2003-04-16

<td> Material</td><td> %</td><td></td><td> %</td><td> Mn</td>

<td> PDL 3000 g/mol</td><td> 50</td><td> PLGA 7000 g/mol</td><td> 50</td><td> 65.000</td>

<td> PDL 3000 g/mol</td><td> 40</td><td> PLGA 7000 g/mol</td><td> 60</td><td> 55.000</td>

<td> PDL 2000 g/mol</td><td> 50</td><td> P-DL-LA 6000 g/mol</td><td> 50</td><td> 87.000</td>

<td> PDL 2000 g/mol</td><td> 40</td><td> P-DL-LA 6000 g/mol</td><td> 60 .</td><td> 72.000</td>

<td> PDL 2000 g/mol</td><td> 50</td><td> P-DL-LA 10000 g/mol</td><td> 50</td><td> 63.000</td>

Mechanical properties:

<td> Material</td><td> Temp.</td><td> E-Modulus MPa</td><td> Tensile stretch</td>

<td> PDL-3k-co-P-DL-LA6k 50/50</td><td> 20’C</td><td> 279</td><td> 453%</td>

<td> PDL-3k-co-P-DL-LA6k 50/50</td><td> 50°C</td><td> 31</td><td> 303 %</td>

<td> PDL-3k-C0-P-DL-l A6k 50/50</td><td> 55^eC</td><td> 25</td><td> 276 %</td>

PDL-3k-co-P-DL-|_A6k 50/50: copolyester urethane, comprising segments of PDL and P DL-LA having an Mn of 3000 and 6000 g/mol, respectively, and comprising 50 et-% of each of the segments PDL and P-DL-LA, respectively

Shape Memory Properties:

<td> Material</td><td> Number of cycles</td><td> Recovery %</td><td> Fixity %</td>

<td> PDL-3k-co-P-DL-LA6k 50/50</td><td> 1</td><td> 46,5</td><td> 98,4</td>

<td> PDL-3k-CO-P-DL-LA6k 50/50</td><td> 2</td><td> 87,3</td><td> 98,8</td>

<td> PDL-3k-co-P-DL-LA6k 50/50</td><td> 3</td><td> 96,8</td><td> 99,1</td>

<td> PDL-3k-co-P-DL-LA6k 50/50</td><td> 4</td><td> 97,9</td><td> 98,5</td>

<td> PDL-3k-co-P-DL-LA6k 50/50</td><td> 5</td><td> 98,2</td><td> 98,5</td>

Blends

The following blends were prepared and evaluated:

Blends comprising PDL

CA 02426740 2003-04-16

Additives were mixed with a PDL polyester urethane having the composition PDL-3kco-PCL-10k 40/60.

The following additive components were added in amounts of from 0.5 to 25 wt.-%:

Colorant (master batch comprising PDL-3k-co-PCL-10k 40/60 and about 5 to 10 wt.-% colorant) nano-ellver barium sulfate

For a blend comprising 10 wt-% of the colored master batch the following shape memory properties were obtained:

Shape Memory Properties:

<td> Material</td><td> Number of cycles</td><td> Recovery %</td><td> Fixity %</td>

<td> 90% PDL-3k-CO-PCL-10k 40/60 10% master batch blue</td><td> 1</td><td> 30,5</td><td> 98,3</td>

<td> 90% PDL-3k-CO-PCL-10k 40/60 10% master batch blue</td><td> 2</td><td> 93,3</td><td> 98,5</td>

<td> 90% PDL-3k-CO-PCL-10k 40/60 10% master batch blue</td><td> 3</td><td> 96,5</td><td> 99,5</td>

<td> 90% PDL-3k-co-PCL-10k 40/60 10% master batch blue</td><td> 4</td><td> 98,6</td><td> 98,6</td>

<td> 90% PDL-3k-co-PCL-10k 40/60 10% master batch blue</td><td> 5</td><td> 99,2</td><td> 98,9</td>

Also blends with commercially available polymers, such as PE or PVC, when using of from 50% to 90% PDL-poiyurethane satisfactory shape memory properties, which correspond to those given above.

Shape Memory Giends

CA 02426740 2003-04-16

These blends are mixtures of pure PDL-polyurethanes with PCL and PCLpolyurethanene, respectively. Only after a combination of the two materials yields a shape memory material. For preparing those blends both materials, the PDLpolyurethane and PCL or PCL-polyurethane are dissolved together and are subsequently precipitated (co-precipitation). In addition blends were prepared in the melt using a compounder (twin screw extruder).

Components employed:

A: PDL-3k-poiyurethane , Mn 95.000 B: PCL-1 Ok-polyurethane, Mn 102.000 C: PCL; Mn 80.000

With a content of the PDL-component of from 20% - 80 % good shape memory properties were obtained. In particular using blend compositions with blend ratios of 40/60 ; 50/50; 60/40 correspond, as far as shape memory properties are concerned, to PDL-co-PCL-polyurethanes,

<td> Material</td><td> Number of cycles</td><td> Recovery %</td><td> Fixity %</td>

<td> 40% PDL-3k-polyurethane 60% PCL-1 Ok-poiyurethane</td><td> 1</td><td> 55,5</td><td> 98,2</td>

<td> 40% PDL-3k-polyurethane 60% PCL-1 Ok-polyurethane</td><td> 2</td><td> 97,3</td><td> 98,2</td>

<td> 40% PDL-3k-polyurethane 60% PCL-1 Ok-polyurethane</td><td> 3</td><td> 98,5</td><td> 99,1</td>

<td> 40% PDL-3k-poiyurethane 60% PCL-1 Ok-polyurethane</td><td> 4</td><td> 98,6</td><td> 98,6</td>

<td> 40% PDL-3k-polyurethane 60% PCL-1 Ok-polyurethane</td><td> 5</td><td> 99,1</td><td> 98,9</td>

PDL-Polvester urethanes: bio compatabiKty/degradation behaviour

CA 02426740 2003-04-16

Experiments were carried out regarding the degradation behaviour of the resorbable materials. Degradation studies were conducted at body temperature (37®C) in aqueous buffered solutions (phosphate buffer, pH 7, comprising NazHPCL, K2HPO4 and NaNa). in order to obtain estimates above long term behaviour so called accelerated degradation studies were carried out at 70°C. For the purpose of this evaluation samples are taken at defined times and molecular weight (Mn) as welt as relative weight loss (%) are determined.

In the following table the results of evaluations for the material PDL-2k-co-PCL-iOk are listed.

<td></td><td></td><td> T 70^eC</td>

<td> Week</td><td> Mn [g/moi]</td><td> Weight loss [%]</td>

<td> 0</td><td></td><td> 185.000</td>

<td> 1</td><td> 0,08</td><td> 175.000</td>

<td> 2</td><td> 0.11</td><td> 152.000</td>

<td> 3</td><td> 0,16</td><td> 134.000</td>

<td> 4</td><td> 0,19</td><td> 76.314</td>

<td> 6</td><td> 0,24</td><td> 27.054</td>

<td> 8</td><td> 0,29</td><td> 8,769</td>

<td> 12</td><td> 5,90</td><td> 2.178</td>

<td> 16</td><td> 22,65</td><td> 2.469</td>

<td> 21</td><td> 41,61</td><td> 2.123</td>

<td> 25</td><td> 49.36</td><td> 3.061</td>

<td> 29</td><td> 53,06</td><td> 2.976</td>

<td></td><td></td><td> T = 37’C</td>

<td> iuaqL· WvCR</td><td> Mn [g/mol]</td><td> Weight loss [%]</td>

<td> 0</td><td> 185.000</td><td> 0</td>

<td> 2</td><td> 184.000</td><td> 0,06</td>

<td> 6</td><td> 183,000</td><td> 0,12</td>

<td> 10</td><td> 184.000</td><td> 0,15</td>

<td> 18</td><td> 182.000</td><td> 0,17</td>

<td> 29</td><td> 180.000</td><td> 0,20</td>

<td></td><td></td><td></td>

<td></td><td></td><td></td>

<td></td><td></td><td></td>

<td></td><td></td><td></td>

<td></td><td></td><td></td>

<td></td><td></td><td></td>

CA 02426740 2003-04-16

In the following table the results of the degradation experiment using the material PDL3k-co-PCL-10kare listed.

<td></td><td colspan="2"> T = 70°C</td><td></td><td></td><td></td><td> T = 37°C</td>

<td> week</td><td> Mn [g/mol]</td><td> Weight loss [%]</td><td></td><td> week</td><td> Mn (g/mol]</td><td> Weight loss [%]</td>

<td> 0</td><td> 185.000</td><td> 0</td><td></td><td> 0</td><td> 185.000</td><td> 0</td>

<td> 1</td><td> 182.000</td><td> 0,05</td><td></td><td> 2</td><td> 184.000</td><td> 0,08</td>

<td> 2</td><td> Ï60.000</td><td> 0,11</td><td></td><td> 6</td><td> 183,000</td><td> 0.15</td>

<td> 3</td><td> .123.000</td><td> 0,15</td><td></td><td> 10</td><td> 184.000</td><td> 0,18</td>

<td> 4</td><td> 112.000</td><td> 0.18</td><td></td><td> 18</td><td> 182.000</td><td> 0,20</td>

<td> 6</td><td> 49.000</td><td> 0,21</td><td></td><td> 29</td><td> 180.000</td><td> 0,22</td>

<td> 8</td><td> 17.500</td><td> 0,41</td><td></td><td></td><td></td><td></td>

<td> 12</td><td> Ϊ0.000</td><td> 6.47</td><td></td><td></td><td></td><td></td>

<td> 16</td><td> 7.300</td><td> 23,98</td><td></td><td></td><td></td><td></td>

<td> 21</td><td> 4.200</td><td> 43,54</td><td></td><td></td><td></td><td></td>

<td> 25</td><td> 3.500</td><td> 50,46</td><td></td><td></td><td></td><td></td>

<td> 29</td><td> 2.500</td><td> 54,15</td><td></td><td></td><td></td><td></td>

In addition the samples were evaluated under a microscope regarding possible surface modifications. A distinct change in the morphology of the surface could be detected.

Bio compatability studies:

For selected materials (PDL-3k-co-PCL-10k; PDL^k-co-PCL-IOk) experiments were carried out regarding the biological evaluation far medicinal products in accordance with ISO/EN/DIN 109Ô3-5 (cytotoxicity). Samples were sterilised, prior to these experiments with ethylene oxide (EO).

Cytotoxicity evaluations were carried out using direct contact with the murine fibroblast cell line L929 (BioWrthaker BE71-131F). Control of membrane integrity was carried out

CA 02426740 2003-04-16 by PA 17 vital coloration (vital cells are colored green). Morphology of the cells after 24h incubation was evaluated using Pa 13 hamaiaun coloration.

Evaluation:

For bith samples membrane integrity was not affected by the materials of the present invention.

The morphology of the cells on the samples Is, compared with the negative control, not changed. Cell apparence of the culture and the seeding efficience on the material correspond to that of the negative control

Processing of PDL-poivester urethanes

Fo.am ejawion:

After extruding and pelletizing the polymer, the polymer, in a second work up, is mixed with a master batch in a double srew extruder (chemical foaming agent Hydrocerol CT 572, product of Clariant), in order to obtain a foam (5% foaming agent, 95% PPDL-3k-coPCL10k). The material, in the form of the rod in the temporary shape is comprssed to 25 % of the initial diameter. Subsequently the rod is expanded again by heating the compressed rod. The initial (permanent) shape is recovered, during this recovery a force of SON is exerted by the material.

Foams by TIPS

A further method for producing porous structures is the «thermally indiced phase separation’ (TIPS) eingesetzt A polymer solution (dioxan, 1 to 25 wt.-% polymer) is cooled at a defined gradient (from 60’C to 3^eC). During cooling a liquid-liquid separation occurs first. Further cooling solidifies the formed phase structure. Using the material PDL-3k-co-PCL1 Ok a foam could be produced. The solvent was removed using a high vacuum.

.Prp_a.r3tion of micro carriers (d 100 nm - 800 urrt

Preparation of microbeads from PDL-3k-co-PCL!0k. Using an emulgator (PVA) an oil-inwater emulsion was prepared. By carfuiiy removing the solvent spherical micro earners were obtained. Using SEM a broad distribution of the particle size was found, as well as a non-uniformity regarding the particle shape. On average the particle size was in the

CA 02426740 2003-04-16 range of from 100 to 200 pm, with the most part of the carriers showing a sperical shape. SEM evaluations furthermore showed that most of the carriers were hollow an collapsing under toe electron beam. Evaluations of single carriers revealed that they showed a smooth surface having some sort of structure within toe nanometer range.

The present invention provides novel polyester urethanes, which enable a controlled adjustment of desired profile of properties. The starting materials to be used are usual compounds, which are available without to much effort The reactions to be used for preparing toe prepolymers (macrodiols) are typical operations in toe field of polymer chemistry, so that the polyester urethanes of the present invention may be obtained in a simple and efficient manner. The present invention enables to overcome the drawbacks of the known materials described above.