碳酸三甲烯
丙交酯
降级(电信)
聚酯纤维
自催化
聚合物
动力学
材料科学
高分子化学
碳酸盐
可生物降解聚合物
共聚物
化学工程
聚合物降解
化学分解
摩尔质量分布
化学
有机化学
催化作用
复合材料
分解
工程类
物理
计算机科学
电信
量子力学
作者
Lihuang Wu,Zixiang Wu,Yuqi Wang,Lu Han,Hongli Mao,Zhongwei Gu
标识
DOI:10.1016/j.polymdegradstab.2022.110183
摘要
Biodegradable poly(trimethylene carbonate) (PTMC) and its copolymers have been widely used in the biomedical field. However, the unclear degradation behavior and kinetics of these biodegradable polymers are major obstacles to their practical application. The precise control of their degradation kinetics remains a challenge, and the relationship between chemical structure and degradation behavior requires further elucidation. In this work, poly(trimethylene carbonate-co-L-lactide) (PTLA) with different chemical compositions at a high number average molecular weight (Mn, ∼550 kDa) has been prepared via ring-opening copolymerization. The in vitro enzymatic degradation and in vivo degradation of PTLA were investigated and the degradation behaviors were found to change from surface to bulk degradation with the increase of lactide content. PTLA with lactide content of 10–30 mol% followed a surface degradation similar to PTMC, with a linear decrease of mass loss rate constant from 1.49 to 0.51 mg/cm2/d, and thickness loss from 15.08 to 4.06 μm/d. PTLA with lactide content > 30 mol% showed typical bulk degradation behaviors similar to aliphatic polyesters, with the polymer chain experiencing an autocatalytic scission occurring prior to the matrix collapse. Therefore, the in vivo degradation kinetics of PTLA with tunable degradation behaviors by chemical composition was finally obtained.
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