Synthesis and in vitro degradation of copolymers of glycolide and 6 (R,S)-methylmorpholine-2,5-dione
✍ Scribed by Fusheng Du; Weiping Ye; Zhongwei Gu; Jiyuan Yang
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 214 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
✦ Synopsis
Copolymerization of glycolide (GA) and 6(R,S)-methylmorpholine-2,5-dione (MMD) was carried out in bulk using stannous octoate as an initiator. The effects of temperature, time, concentration of stannous octoate, and the feed composition on the copolymerization were investigated. DSC analysis showed that glass transition temperature ( T g ) of the resulting copolymers (PGM) increased with increase of MMD content in the copolymers, while melting temperature ( T m ) and heat of fusion ( DH) decreased. In vitro degradation was performed in two media: PBS buffer (pH 7.4) and distilled water (pH 6.8). It showed that the erosion rates increased with increasing MMD content in the original copolymers, and the degradation proceeded more rapidly in PBS buffer than in distilled water. Based on the changes of composition and crystallinity of the samples during the degradation, it is suggested that the degradation proceeded through two main stages: first, mainly in amorphous regions and then in crystalline ones.
📜 SIMILAR VOLUMES
## Abstract Cyclic carbonate 9‐phenyl‐2,4,8,10‐tetraoxaspiro‐[5,5]undcane‐3‐one is a six‐membered carbonate monomer with a rigid side group. Novel biodegradable poly(carbonate‐ester), poly(9‐phenyl‐2,4,8,10‐tetraoxaspiro‐[5,5]undecan‐3‐one‐__co__‐D,L‐lactide) P(CC‐__co__‐DLLA), was synthesized by r
ABA type block copolymers with poly[3(S)-isobutylmorpholine-2,5-dione] (PIBMD, A) and poly(ethylene oxide) (M n = 6 000, PEO, B) blocks, PIBMD-b-PEO-b-PIBMD, were synthesized via ringopening polymerization of 3(S)-isobutylmorpholine-2,5-dione in the presence of hydroxytelechelic poly-(ethylene oxide