College of Pharmacy, Freie Universität Berlin, Kelchstr. 31, 12169 Berlin, Germany.
College of Pharmacy, Freie Universität Berlin, Kelchstr. 31, 12169 Berlin, Germany.
Int J Pharm. 2024 Nov 15;665:124737. doi: 10.1016/j.ijpharm.2024.124737. Epub 2024 Sep 20.
The removal of residual solvents from biodegradable poly(D,L-lactide-co-glycolide) (PLGA) microparticles by fluidized bed drying was investigated. Microparticles were prepared by the O/W solvent extraction/evaporation method and the influence of various process and formulation parameters on the secondary drying was studied. PLGA microparticles and films were characterized for residual organic solvent and water content, recrystallisation, surface morphology, drug loading and in-vitro release of the drugs dexamethasone and risperidone. While alcohol-free fluidized bed drying decreased the residual dichloromethane content only from about 7 % (w/w) to 6.4 % (w/w) (18 °C) or 3.2 % (w/w) (35 °C) within 24 h, 140 mg/L methanol vapor in purge gas facilitated almost complete removal of dichloromethane or ethyl acetate from microparticles (0-0.11 % (w/w) after 6 h). By controlling the alcohol concentration and temperature of the purge gas, the alcohol absorption and complete removal was controlled. Risperidone increased the methanol absorption enhancing the plasticization. A high initial residual water content was identified to promote aggregation and was eliminated by starting fluidized bed drying without alcohol. Alcohol vapor-assisted fluidized bed drying accelerated microparticle manufacturing without affecting the redispersibility, the drug loading and the in-vitro release of risperidone and dexamethasone.
采用流化床干燥法去除可生物降解的聚(D,L-丙交酯-共-乙交酯)(PLGA)微球中的残留溶剂。采用 O/W 溶剂萃取/蒸发法制备微球,并研究了各种工艺和配方参数对二次干燥的影响。对 PLGA 微球和薄膜的残留有机溶剂和水分含量、重结晶、表面形态、药物包封和药物地塞米松和利培酮的体外释放进行了表征。在 24 小时内,无醇流化床干燥仅将二氯甲烷的残留含量从约 7%(w/w)降低至 6.4%(w/w)(18°C)或 3.2%(w/w)(35°C),而在吹扫气体中 140mg/L 的甲醇蒸气有助于从微球中几乎完全去除二氯甲烷或乙酸乙酯(6 小时后为 0-0.11%(w/w))。通过控制吹扫气体的酒精浓度和温度,可以控制酒精的吸收和完全去除。利培酮增加了甲醇的吸收,增强了塑性。高初始残留水分含量被确定为促进聚集,并通过在没有酒精的情况下开始流化床干燥来消除。醇蒸汽辅助流化床干燥加速了微球的制造,而不影响利培酮和地塞米松的再分散性、药物包封和体外释放。