壳聚糖和阿拉伯胶制备胰岛素纳米颗粒的体外评价。

ISRN Pharmaceutics Pub Date : 2011-01-01 Epub Date: 2011-07-10 DOI:10.5402/2011/860109
M R Avadi, A M M Sadeghi, Naser Mohamadpour Dounighi, R Dinarvand, F Atyabi, M Rafiee-Tehrani
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引用次数: 42

摘要

基于纳米颗粒的聚合物递送系统已经成为一种很有前途的经口胰岛素递送方法。本研究的目的是研究胰岛素纳米颗粒系统的释放和体外研究。采用离子凝胶法制备纳米颗粒。测定了纳米颗粒的粒径分布、zeta电位和多分散性指数。结果表明,纳米颗粒带正电荷,尺寸分布在170 ~ 200 nm范围内。壳聚糖的正电荷基团与阿拉伯胶的负电荷基团之间的静电相互作用对胰岛素在纳米颗粒中的结合效率起着重要的作用。体外胰岛素释放研究表明,最初的爆发之后是胰岛素的缓慢释放。利用切除的大鼠空肠评价纳米系统的黏附性。体外研究表明,与游离胰岛素相比,壳聚糖纳米颗粒的存在显著增加了胰岛素的吸收。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ex vivo evaluation of insulin nanoparticles using chitosan and arabic gum.

Polymeric delivery systems based on nanoparticles have emerged as a promising approach for peroral insulin delivery. The aim of the present study was to investigate the release of insulin nanoparticulate systems and ex vivo studies. The nanoparticles were prepared by the ion gelation method. Particle size distribution, zeta potential, and polydispersity index of the nanoparticles were determined. It was found that the nanoparticles carried positive charges and showed a size distribution in the range of 170-200 nm. The electrostatic interactions between the positively charged group of chitosan and negatively charged groups of Arabic gum play an important role in the association efficiency of insulin in nanoparticles. In vitro insulin release studies showed an initial burst followed by a slow release of insulin. The mucoadhesion of the nanosystem was evaluated using excised rat jejunum. Ex vivo studies have shown a significant increase in absorption of insulin in the presence of chitosan nanoparticles in comparison with free insulin.

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