van de Weert M, Hennink W E, Jiskoot W
Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, The Netherlands.
Pharm Res. 2000 Oct;17(10):1159-67. doi: 10.1023/a:1026498209874.
In this review the current knowledge of protein degradation during preparation, storage and release from poly(lactic-co-glycolic acid) (PLGA) microparticles is described, as well as stabilization approaches. Although we have focussed on PLGA microparticles, the degradation processes and mechanisms described here are valid for many other polymeric release systems. Optimized process conditions as well as stabilizing excipients need to be used to counteract several stress factors that compromise the integrity of protein structure during preparation, storage, and release. The use of various stabilization approaches has rendered some success in increasing protein stability, but, still, full preservation of the native protein structure remains a major challenge in the formulation of protein-loaded PLGA microparticles.
在本综述中,描述了聚乳酸-乙醇酸共聚物(PLGA)微粒在制备、储存和释放过程中蛋白质降解的现有知识,以及稳定化方法。尽管我们专注于PLGA微粒,但这里描述的降解过程和机制对许多其他聚合物释放系统也是有效的。需要使用优化的工艺条件以及稳定化辅料来对抗在制备、储存和释放过程中损害蛋白质结构完整性的几种应激因素。使用各种稳定化方法在提高蛋白质稳定性方面已取得了一些成功,但是,在制备载有蛋白质的PLGA微粒时,完全保留天然蛋白质结构仍然是一个重大挑战。