Park T G
School of Pharmacy, Temple University, Philadelphia, PA 19140, USA.
Biomaterials. 1995 Oct;16(15):1123-30. doi: 10.1016/0142-9612(95)93575-x.
The in vitro degradation behaviour of a wide range of poly(D,L-lactic-co-glycolic acid) (PLGA) has been examined in terms of degree of degradation and morphological change during an incubation period of up to 53 d. Gel permeation chromatography and differential scanning calorimetry were employed to characterize their degradation profiles. It was found that amorphous PLGA exhibited a transient multiple crystallization behaviour of D- or L-lactic acid oligomers during degradation. This indicated that the hydrolytic scission of ester bonds tends to primarily target the linkage between glycolic acid and D- or L-lactic acid or glycolic acid. In addition, two distinctive glass transition temperatures appeared when these crystallization phenomena occurred, suggesting the transient presence of fast and slowly eroding polymer domains within microspheres during the degradation. This study supports the heterogeneous bulk degradation for PLGA microspheres which has been proposed recently for a large specimen.
在长达53天的孵育期内,从降解程度和形态变化方面对多种聚(D,L-乳酸-共-乙醇酸)(PLGA)的体外降解行为进行了研究。采用凝胶渗透色谱法和差示扫描量热法对其降解曲线进行表征。发现无定形PLGA在降解过程中表现出D-或L-乳酸低聚物的瞬时多重结晶行为。这表明酯键的水解断裂倾向于主要针对乙醇酸与D-或L-乳酸或乙醇酸之间的连接。此外,当这些结晶现象发生时出现了两个明显的玻璃化转变温度,这表明在降解过程中微球内存在快速和缓慢侵蚀的聚合物域的瞬时存在。本研究支持了最近针对大尺寸样本提出的PLGA微球的非均相整体降解。