TY - JOUR
T1 - Rapidly degraded terpolymers of DL‐lactide, glycolide, and ϵ‐caprolactone with increased hydrophilicity by copolymerization with polyethers
AU - Sawhney, Amarpreet S.
AU - Hubbell, Jeffrey A.
PY - 1990/10
Y1 - 1990/10
N2 - A series of 66 terpolymers of dl‐lactide, glycolide, and ϵ‐caprolactone was synthesized for the purpose of identifying those materials which exhibited rapid degradation in vitro. Polymers having half‐lives from a few weeks to several months were identified. The morphology of each material was scanning calorimetry. A terpolymeric composition of 60% glycolide, 30% dl‐lactide, and 10% ϵ‐caprolactone, which exhibited a half‐life of 17 days, was selected for further investigation. The hydrophilicity of this material was increased by performing the polymerization in the presence of a polyether prepolymer, Pluronic F‐68, with the motivation of concomitantly reducing cell and tissue adhesion. An increase in the hydrophilicty of the material was apparent from contact angle measurements. Copolymerization with the prepolymer also resulted in a stronger and partly crystalline material which was mechanically stable at physiological temperature in water. A slight increase was observed in the half‐life of the polymer relative to the base polymer due to the presence of the prepolymer.
AB - A series of 66 terpolymers of dl‐lactide, glycolide, and ϵ‐caprolactone was synthesized for the purpose of identifying those materials which exhibited rapid degradation in vitro. Polymers having half‐lives from a few weeks to several months were identified. The morphology of each material was scanning calorimetry. A terpolymeric composition of 60% glycolide, 30% dl‐lactide, and 10% ϵ‐caprolactone, which exhibited a half‐life of 17 days, was selected for further investigation. The hydrophilicity of this material was increased by performing the polymerization in the presence of a polyether prepolymer, Pluronic F‐68, with the motivation of concomitantly reducing cell and tissue adhesion. An increase in the hydrophilicty of the material was apparent from contact angle measurements. Copolymerization with the prepolymer also resulted in a stronger and partly crystalline material which was mechanically stable at physiological temperature in water. A slight increase was observed in the half‐life of the polymer relative to the base polymer due to the presence of the prepolymer.
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U2 - 10.1002/jbm.820241011
DO - 10.1002/jbm.820241011
M3 - Article
C2 - 2283356
AN - SCOPUS:0025500374
SN - 0021-9304
VL - 24
SP - 1397
EP - 1411
JO - Journal of Biomedical Materials Research
JF - Journal of Biomedical Materials Research
IS - 10
ER -