胶束
分散性
PEG比率
粒径
化学工程
溶剂
化学
冷冻干燥
400号桩
共聚物
活性成分
材料科学
泊洛沙姆
色谱法
聚乙二醇
高分子化学
有机化学
水溶液
聚合物
药理学
物理化学
医学
工程类
经济
财务
作者
Morteza Rasoulianboroujeni,Lauren Repp,Hye Jin Lee,Glen S. Kwon
标识
DOI:10.1016/j.jconrel.2022.08.032
摘要
A new approach named PEG-assist is introduced for the production of drug-loaded polymeric micelles. The method is based on the use of PEG as the non-selective solvent for PEG-b-PLA in the fabrication procedure. Both hydration temperature and PEG molecular weight are shown to have a significant effect on the encapsulation efficiency of PTX in PEG4kDa-b-PLA2kDa micelles. The optimal procedure for fabrication includes the use of PEG1kDa as the solvent at 60 °C, cooling the mixture to 40 °C, hydration at 40 °C, freezing at -80 °C and freeze-drying at -35 °C, 15 Pa. No significant difference (p > 0.05) in PTX encapsulation, average particle size and polydispersity index is observed between the samples before freeze-drying and after reconstitution of the freeze-dried cake. The prepared PTX formulations are stable at room temperature for at least 8 h. Scaling the batch size to 25× leads to no significant change (p > 0.05) in PTX encapsulation, average particle size and polydispersity index. PEG-assist method is applicable to other drugs such as 17-AAG, and copolymers of varied molecular weights. The use of no organic solvent, simplicity, cost-effectiveness, and efficiency makes PEG-assist a very promising approach for large scale production of drug-loaded polymeric micelles.
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