School of Chemical and Biomedical Engineering, Nanyang Technological University, 70 Nanyang Drive, Singapore, 637457, Singapore.
NTU-Northwestern Institute of Nanomedicine, Interdisciplinary Graduate School, Nanyang Technological University, 50 Nanyang Avenue, Singapore, 639798, Singapore.
Nanoscale Res Lett. 2016 Dec;11(1):9. doi: 10.1186/s11671-015-1222-7. Epub 2016 Jan 8.
Core-shell alginate-poly (lactic-co-glycolic) acid (PLGA) microparticles are potential candidates to improve hydrophilic drug loading while facilitating controlled release. This report studies the influence of the alginate core size on the drug release profile of alginate-PLGA microparticles and its size. Microparticles are synthesized through double-emulsion fabrication via a concurrent ionotropic gelation and solvent extraction. The size of alginate core ranges from approximately 10, 50, to 100 μm when the emulsification method at the first step is homogenization, vortexing, or magnetic stirring, respectively. The second step emulsification for all three conditions is performed with magnetic stirring. Interestingly, although the alginate core has different sizes, alginate-PLGA microparticle diameter does not change. However, drug release profiles are dramatically different for microparticles comprising different-sized alginate cores. Specifically, taking calcein as a model drug, microparticles containing the smallest alginate core (10 μm) show the slowest release over a period of 26 days with burst release less than 1 %.
核壳结构的海藻酸钠-聚(乳酸-共-乙醇酸)(PLGA)微球是提高亲水性药物载量同时实现药物控制释放的潜在候选材料。本报告研究了海藻酸钠核大小对海藻酸钠-PLGA 微球及其粒径的药物释放特性的影响。微球通过双乳液法制备,采用离子凝胶化和溶剂萃取同步进行。当第一步乳化方法分别为均化、涡旋或磁力搅拌时,海藻酸钠核的大小分别约为 10、50 和 100μm。对于所有三种条件,第二步乳化均采用磁力搅拌。有趣的是,尽管海藻酸钠核具有不同的大小,但包含不同大小海藻酸钠核的海藻酸钠-PLGA 微球的直径没有变化。然而,药物释放特性对于具有不同大小海藻酸钠核的微球有显著差异。具体来说,以钙黄绿素为模型药物,含有最小海藻酸钠核(10μm)的微球在 26 天的时间内显示出最慢的释放,突释小于 1%。