PLGA公司
乙醇酸
纳米颗粒
乳状液
化学工程
化学
乳酸
可生物降解聚合物
控制释放
溶剂
丙交酯
核化学
材料科学
高分子化学
有机化学
聚合物
纳米技术
共聚物
工程类
生物
细菌
遗传学
作者
Rezaul Haque Ansary,Mohd Shukrimi Awang,M. M. Rahman
标识
DOI:10.4314/tjpr.v13i7.24
摘要
Biodegradable poly(D, L-lactide-co-glycolide) (PLGA) and PLGA-based polymeric nanoparticles are widely used for sustained release of protein and peptide drugs.These formulations are usually prepared by water/oil/water (W/O/W) and solid/oil/water (S/O/W) double emulsion solvent evaporation method.Other methods of preparation are nanoprecipitation, emulsion solvent diffusion and salting-out.This review attempts to address the effects of PLGA molecular weight, lactide to glycolide ratio, crystallinity, hydrophilicity as well as nanoparticles preparation variables (e.g., homogenizer speed, surfactants nature and concentration) on the size, morphology, drug encapsulation efficiency and release profile of PLGA mico/nanoparticles.The current knowledge of protein instability during preparation, storage and release from PLGA micro/nanoparticles and protein stabilization approaches has also been discussed in this review.
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