Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin, 777 Highland Avenue, Madison, WI 53705, United States.
Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin, 777 Highland Avenue, Madison, WI 53705, United States.
J Control Release. 2022 Oct;350:350-359. doi: 10.1016/j.jconrel.2022.08.032. Epub 2022 Aug 26.
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 PEG-b-PLA micelles. The optimal procedure for fabrication includes the use of PEG 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.
一种名为 PEG-辅助的新方法被引入用于制备载药聚合物胶束。该方法基于在制备过程中使用 PEG 作为 PEG-b-PLA 的非选择性溶剂。水合温度和 PEG 分子量都对 PTX 在 PEG-b-PLA 胶束中的包封效率有显著影响。最佳制备工艺包括在 60°C 下使用 PEG 作为溶剂,将混合物冷却至 40°C,在 40°C 下水化,在-80°C 下冷冻,在-35°C、15 Pa 下冷冻干燥。在冻干前和冻干后重新配制冻干蛋糕之间,观察到 PTX 包封率、平均粒径和多分散指数没有显著差异(p>0.05)。在室温下,制备的 PTX 制剂至少稳定 8 小时。将批量放大至 25×,PTX 包封率、平均粒径和多分散指数没有显著变化(p>0.05)。PEG-辅助方法适用于其他药物,如 17-AAG 和不同分子量的共聚物。不使用有机溶剂、简单、经济高效,使 PEG-辅助成为大规模制备载药聚合物胶束的一种很有前途的方法。