聚合
己内酯
共聚物
聚合物
材料科学
开环聚合
丙交酯
可生物降解聚合物
高分子化学
纳米技术
复合材料
作者
Chenmin Luo,Shengyang Liu,Wei Luo,Jing Wang,Hongyan He,Can Chen,Lan Xiao,Changsheng Liu,Yulin Li
标识
DOI:10.1002/mabi.202200507
摘要
Abstract Biodegradable materials are pivotal in the biomedical field, where how to precisely control their structure and performance is critical for their translational application. In this study, poly(L‐lactide‐ b ‐ ε ‐caprolactone) block copolymers (bPLCL) with well‐defined segment structure are obtained by a first synthesis of poly(ε‐caprolactone) soft block, followed by ring opening polymerization of lactide to form poly(L‐lactide acid) hard block. The pre‐polymerization allows for fabrication of bPLCL with the definite compositions of soft/hard segment while preserving the individual segment of their special soft or hard segment. These priorities make the bPLCL afford biodegradable polymer with better mechanical and biodegradable controllability than the random poly(L‐lactide‐co‐ε‐caprolactone) (rPLCL) synthesized via traditional one‐pot polymerization. 10 mol% ε ‐caprolactone introduction can result in a formation of an elastic polymer with elongation at break of 286.15% ± 55.23%. Also, bPLCL preserves the unique crystalline structure of the soft and hard segments to present a more sustainable biodegradability than the rPLCL. The combinative merits make the pre‐polymerization technique a promising strategy for a scalable production of PLCL materials for potential biomedical application.
科研通智能强力驱动
Strongly Powered by AbleSci AI