Mao Shirui, Xu Jing, Cai Cuifang, Germershaus Oliver, Schaper Andreas, Kissel Thomas
Department of Pharmaceutics and Biopharmacy, Philipps Universität Marburg, Ketzerbach 63, D-35032 Marburg, Germany.
Int J Pharm. 2007 Apr 4;334(1-2):137-48. doi: 10.1016/j.ijpharm.2006.10.036. Epub 2006 Oct 28.
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.
以异硫氰酸荧光素标记的葡聚糖(FITC - 葡聚糖40,FD40)作为亲水性模型化合物,采用W/O/W双乳液技术制备微球。研究了工艺参数对微球形态以及FD40从聚乳酸 - 羟基乙酸共聚物(PLGA)微球中的突释的影响。通过冷冻切片技术和扫描电子显微镜(SEM)的体视学方法研究了微球的内部形态。用共聚焦激光扫描显微镜(CLSM)观察了微球中的药物分布。聚合物性质(RG503和RG503H)对微球的微观形态有显著影响。连续水相体积(W2)的增加导致表面孔隙率增加,但内部孔隙率降低。将连续相中聚乙烯醇(PVA)的浓度从0.1%提高到1%时,粒径变化不大,但突释从12.2%降至5.9%。微球的内部孔隙率随聚合物浓度的增加而显著降低。初乳制备过程中匀化速度的增加导致内部孔隙率降低。突释随载药量的增加而降低,但随药物分子量的增加而增加。微球中的药物分布取决于制备方法。在扩散阶段,微球的孔隙率随时间降低,但在生物侵蚀阶段,内部形态对释放行为没有影响。总之,在以孔隙扩散为特征的初始释放阶段,表面孔隙率和内部形态对亲水性大分子从可生物降解微球中的释放起着重要作用。