PLGA公司
微球
药物输送
纳米技术
膜乳化
药品
控制释放
毒品携带者
材料科学
药理学
体内
生物医学工程
加药
喷雾干燥
封装(网络)
输送系统
纳米医学
医学
靶向给药
化学
微粒
粒径
翻译(生物学)
作者
Sai Qian,Lan Ma,Chenlu Liu,Yuxi Lin,Jianmin Wu,Xiaolian Wang
摘要
Poly(lactic-co-glycolic acid) (PLGA) microspheres are a clinically established platform for sustained and controlled drug delivery, offering tunable degradation and reduced dosing frequency. This review critically appraises PLGA microsphere technology, linking materials science with clinical translation. We examine how molecular parameters-molecular weight, lactide-to-glycolide ratio, and terminal group chemistry-affect degradation and release kinetics. Key fabrication methods (emulsion-solvent evaporation, spray drying, membrane emulsification, and microfluidics) are compared for their control over encapsulation efficiency, particle size, and scalability. Release mechanisms, including diffusion, swelling, and erosion, are discussed alongside strategies to mitigate burst release. The review also addresses in vivo pharmacokinetics, recent clinical progress in oncology and vaccine delivery, regulatory challenges, manufacturing hurdles, and future directions such as stimuli-responsive microspheres and AI-guided formulation design.
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