降级(电信)
水解
丙交酯
水解降解
共聚物
生物降解
乳酸
无定形固体
苹果酸
化学工程
材料科学
高分子化学
可生物降解聚合物
微观结构
化学
聚合物
有机化学
复合材料
柠檬酸
细菌
工程类
生物
电信
遗传学
计算机科学
作者
Hideko Tamaru Oyama,Daisuke Tanishima,Ryohei Ogawa
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2017-03-09
卷期号:18 (4): 1281-1292
被引量:32
标识
DOI:10.1021/acs.biomac.7b00016
摘要
Although poly(l-lactic acid) (PLLA) is reputed to be biodegradable in the human body, its hydrophobic nature lets it persist for ca. 5.5 years. This study demonstrates that biologically safe lactide copolymers, poly(aspartic acid-co-l-lactide) (PAL) and poly(malic acid-co-l-lactide) (PML), dispersed in the PLLA function as detonators (triggers) for its hydrolytic degradation under physiological conditions. The copolymers significantly enhance hydrolysis, and consequently, the degradation rate of PLLA becomes easily tunable by controlling the amounts of PAL and PML. The present study elucidates the effects of uniaxial drawing on the structural development, mechanical properties, and hydrolytic degradation under physiological conditions of PLLA blend films. At initial degradation stages, the mass loss was not affected by uniaxial drawing; however, at late degradation stages, less developed crystals as well as amorphous chains were degradable at low draw ratio (DR), whereas not only highly developed crystals but also the oriented amorphous chains became insensitive to hydrolysis at high DR. Our work provides important molecular level results that demonstrate that biodegradable materials can have superb mechanical properties and also disappear in a required time under physiological conditions.
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