聚乳酸
PLGA公司
乙醇酸
降级(电信)
共聚物
结晶
材料科学
水解
化学工程
热稳定性
生物降解
聚合物
无定形固体
高分子化学
乳酸
水解降解
化学
有机化学
复合材料
纳米技术
纳米颗粒
细菌
工程类
生物
电信
遗传学
计算机科学
作者
Zeyu Chen,Xi Zhang,Ye Fu,Yu Jin,Yunxuan Weng,Xinchao Bian,Xuesi Chen
出处
期刊:Polymers
[MDPI AG]
日期:2024-06-21
卷期号:16 (13): 1765-1765
被引量:15
标识
DOI:10.3390/polym16131765
摘要
Poly(lactic acid) (PLA) and poly(glycolic acid) (PGA) are extensively studied biodegradable polymers. However, the degradation behavior of their copolymer, poly(lactic-co-glycolic acid) (PLGA), in marine environments has not yet been confirmed. In this study, the changes in macroscopic and microscopic morphology, thermal properties, aggregation, and chemical structure of PLA, PGA, PLGA-85, and PLGA-75 (with 85% and 75% LA content) in simulated marine environments were investigated. Results revealed that degradation occurred through hydrolysis of ester bonds, and the degradation rate of PGA was faster than that of PLA. The amorphous region degraded preferentially over the crystalline region, leading to cleavage-induced crystallization and decreased thermal stability of PLA, PLGA-85, and PLGA-75. The crystal structures of PLGAs were similar to those of PLA, and the higher GA content, the faster was the degradation rate. This study provides a deeper understanding of the seawater degradation behaviors of PLA, PGA, and their copolymers, and provides guidance for the preparation of materials with controllable degradation performance.
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