Cheng Landi, Bulmer Cody, Margaritis Argyrios
Department of Chemical and Biochemical Engineering, the University of Western Ontario, London, Ontario, N6A 5B9, Canada.
Curr Drug Deliv. 2015;12(3):351-7.
The objective of this research project was to develop a nanoparticle drug delivery system using the biopolymer chitosan as the base component. The nanoparticles were produced through ionotropic gelation by flush mixing chitosan with counterions carrageenan and alginate. The nanoparticles were generated under a range of conditions to determine the effect of pH, chitosan concentration, carrageenan concentration, and alginate concentration on the nanoparticle characteristics of particle diameter, zeta potential, and particle size distribution. The encapsulation and controlled release of BSA from chitosan nanoparticles was also evaluated. The encapsulation of BSA was used as a model system for the controlled drug delivery from composite nanoparticles. The release profile indicated an initial burst in the first few hours of the trial, followed by a slower steady release over time. According to Korsmeyer-Peppas model, the release profile followed fickian diffusion.
本研究项目的目标是开发一种以生物聚合物壳聚糖为基础成分的纳米颗粒药物递送系统。通过将壳聚糖与反离子角叉菜胶和海藻酸盐进行快速混合,利用离子凝胶法制备纳米颗粒。在一系列条件下生成纳米颗粒,以确定pH值、壳聚糖浓度、角叉菜胶浓度和海藻酸盐浓度对纳米颗粒粒径、zeta电位和粒径分布等特性的影响。还评估了牛血清白蛋白从壳聚糖纳米颗粒中的包封和控释情况。牛血清白蛋白的包封被用作复合纳米颗粒控释药物的模型系统。释放曲线表明,在试验的最初几个小时内有一个初始突释,随后随着时间的推移有一个较慢的稳定释放。根据Korsmeyer-Peppas模型,释放曲线遵循菲克扩散。