Bioabsorbable polymeric composition for a medical device
View Patent ↗A biodegradable and biocompatible nontoxic polymeric composition is provided which includes a base material such as a crystallizable polymer, copolymer, or terpolymer, and a copolymer or terpolymer additive. Medical devices manufactured from the composition are also provided.
1. A crystallizable bioabsorbable polymer composition comprising a base polymer comprising a poly(L-lactide) moiety, and/or a poly(D-lactide) moiety, and/or poly L-lactide-co-PEG moiety, and/or poly D-lactide-co-PEG moiety, linked with a modifying copolymer thereof, comprising poly(L-lactide-co-Tri-methylene-carbonate) or poly(D-lactide-co-tri-methylene-carbonate) or poly(L-lactide-co-ε-caprolactone) or poly(D-lactide-co-ε-caprolactone) in the form of block copolymers or blocky random copolymers, wherein the thermal transition temperature of the crystallizable bioabsorbable polymer composition ranges from about 60° C. to about 70° C., and wherein the crystallizable bioabsorbable polymer composition forms at least part of a stent.
2. The crystallizable bioabsorbable polymer composition of claim 1 , wherein the thermal transition temperature of the bioabsorbable polymer ranges from about 61° C. to about 66° C.
3. The crystallizable bioabsorbable polymer composition of claim 1 , wherein the thermal transition temperature of the bioabsorbable polymer is about 61° C.
4. The crystallizable bioabsorbable polymer composition of claim 1 , wherein the thermal transition temperature of the bioabsorbable polymer is about 66° C.
5. The crystallizable bioabsorbable polymer composition of claim 1 , wherein the thermal transition temperature of the bioabsorbable polymer is about 64° C.
6. The crystallizable bioabsorbable polymer composition of claim 1 , wherein the base polymer is poly L-lactide.
7. The crystallizable bioabsorbable polymer composition of claim 1 , wherein the modifying copolymer is poly L-lactide-co-TMC.
8. The crystallizable bioabsorbable polymer composition of claim 1 , wherein a residual monomer concentration of the composition is less than about 0.5%.