The present invention relates to biodegradable copolyesters with molecular weight Mn from 10 000 to 100 000 measured by GPC, obtainable via reaction of i) from 51 to 84% by weight, based on the copolyester, of a branched polyester middle block produced from aliphatic or aliphatic and aromatic dicarboxylic acids and from aliphatic dihydroxy compounds with molecular weight Mn from 5000 to 25 000 measured by .sup.1H NMR with from 15.9 to 48.9% by weight, based on the copolyester, of a lactide in the presence of a catalyst, and then the resultant polyester triblock with molecular weight Mn measured by .sup.1H NMR from 5800 to 49 500 with ii) from 0.1 to 3% by weight, based on the copolyester, of a diisocyanate.

The present invention further relates to a process for the production of, and to the use of, the abovementioned biodegradable copolyesters.

Phase segregated block-copolymer based on repeating structural elements represented by formula I ##STR00001## wherein PHA represents at least one block based on one or more α-hydroxy acids, PDAS represents a central block based on a dialkylsiloxane, the PDAS block has a weight average molecular weight in the range of from 4000 to 10000, the blocks PHA have a weight average molecular weight in the range of from 2000 to 10 000, the phase segregated block copolymer has a weight average molecular weight of from 40 000 to 120 000.

A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethylenic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups. Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

The present invention relates to shape-memory polymers, a method for providing said shape-memory polymers, uses and precursors thereof. More precisely, shape-memory polymers according to the present invention comprise end-capped urethane- and/or urea-based polymers having an amorphous backbone. Shape-memory polymers described herein provide for improved properties.

Bioactive liquid formulations are formed of combinations of absorbable, segmented aliphatic polyurethane compositions and liquid polyether for use as vehicles for the controlled release of at least one active agent for the conventional and unconventional treatment of different forms of cancer and the management of at least one type of bacterial, fungal, and viral infection.

The present disclosure provides a crosslinking agent, the preparation process and uses thereof, a hydrogel and a biodegradable cryogel including the crosslinking agent.

A polylactic acid resin composition, which comprises: a hard segment containing a polylactic acid repeat unit; and a soft segment containing a polyurethane polyol repeat unit in which polyether-based polyol repeat units are linearly connected to each other via a urethane linkage, can be processed at low temperatures and at high rates, has a high solidification rate, and is eco-friendly, due to a low melting point thereof, and thus is useful for 3D printing.

A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethyl enic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups, Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

The present invention relates to a polyurethane which is the reaction product of a polyisocyanate and polyester, wherein said polyester is formed from a dimer fatty acid, a C.sub.2 to C.sub.4 diol, and a C.sub.8 to C.sub.16 dicarboxylic acid or C.sub.6 to C.sub.12 lactide. The inventions also relates to a polyester for use in forming the polyurethane of the first aspect, said polyester formed from a dimer fatty acid, a C.sub.2 to C.sub.4 diol, and a C.sub.8 to C.sub.16 dicarboxylic acid or C.sub.6 to C.sub.12 lactide.

Provided are oriented biodegradable thermoplastic polyurethane films. The films may be prepared by extruding and drawing biodegradable polyurethane films. The polyurethanes may be prepared from biodegradable polyols and/or biodegradable chain extenders. The films possess high tensile strength yet are degradable under biological conditions. The films may be utilized in the fabrication of devices, particularly implantable medical devices.