壳聚糖
生物利用度
胰岛素
纳米颗粒
体内
化学
口服
致电离效应
粒径
化学工程
材料科学
聚电解质
生物物理学
核化学
纳米技术
药理学
内科学
医学
聚合物
生物化学
有机化学
生物技术
受体
物理化学
工程类
生物
NMDA受体
作者
Piyasi Mukhopadhyay,Souma Chakraborty,Sourav Bhattacharya,Roshnara Mishra,Patit Paban Kundu
标识
DOI:10.1016/j.ijbiomac.2014.08.040
摘要
Chitosan-alginate (CS/ALG) nanoparticles were prepared by formation of an ionotropic pre-gelation of an alginate (ALG) core entrapping insulin, followed by chitosan (CS) polyelectrolyte complexation, for successful oral insulin administration. Mild preparation process without harsh chemicals is aimed at improving insulin bio-efficiency in in vivo model. The nanoparticles showed an average particle size of 100–200 nm in dynamic light scattering (DLS), with almost spherical or sub-spherical shape and ∼85% of insulin encapsulation. Again, retention of almost entire amount of encapsulated insulin in simulated gastric buffer followed by its sustained release in simulated intestinal condition proved its pH sensitivity in in vitro release studies. Significant hypoglycemic effects with improved insulin-relative bioavailability (∼8.11%) in in vivo model revealed the efficacy of these core-shell nanoparticles of CS/ALG as an oral insulin carrier. No systemic toxicity was found after its peroral treatment, suggesting these core-shell nanoparticles as a promising device for potential oral insulin delivery.
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