Effect of WOW process parameters on morphology and burst release of FITC-dextran loaded PLGA microspheres

多孔性 PLGA公司 扫描电子显微镜 微粒 材料科学 右旋糖酐 形态学(生物学) 聚合物 化学工程 毒品携带者 乳状液 粒径 控制释放 药物输送 化学 色谱法 复合材料 纳米技术 纳米颗粒 工程类 生物 遗传学
作者
Shirui Mao,Jing Xu,Cuifang Cai,Oliver Germershaus,Andreas Schaper,Thomas Kissel
出处
期刊:International Journal of Pharmaceutics [Elsevier BV]
卷期号:334 (1-2): 137-148 被引量:259
标识
DOI:10.1016/j.ijpharm.2006.10.036
摘要

Using fluorescein isothiocyanate labeled dextran (FITC-dextran 40, FD40) as a hydrophilic model compound, microspheres were prepared by a WOW double emulsion technique. Influence of process parameters on microsphere morphology and burst release of FD40 from PLGA microspheres was studied. Internal morphology of microspheres was investigated by stereological method via cryo-cutting technique and scanning electron microscopy (SEM). Drug distribution in microspheres was observed with confocal laser scanning microscopy (CLSM). Polymer nature (RG503 and RG503H) had significant influence on the micro-morphology of microspheres. Increase in continuous water phase volume (W2) led to increased surface porosity but decreased internal porosity. By increasing PVA concentration in the continuous phase from 0.1 to 1%, particle size changed marginally but burst release decreased from 12.2 to 5.9%. Internal porosity of microspheres decreased considerably with increasing polymer concentration. Increase in homogenization speed during the primary emulsion preparation led to decreased internal porosity. Burst release decreased with increasing drug loading but increased with drug molecular weight. Drug distribution in microspheres depended on preparation method. The porosity of microspheres decreased with time in the diffusion stage, but internal morphology had no influence on the release behavior in the bioerosion stage. In summary, surface porosity and internal morphology play a significant role in the release of hydrophilic macromolecules from biodegradable microspheres in the initial release phase characterized by pore diffusion.
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