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pH-Sensitive Polymeric Poly (ε-caprolactone) Core-Chitosan/Alginate Shell Particle System for Oral Insulin Delivery

机译:pH敏感的聚合物聚(ε-二甲酰胺)核心壳聚糖/藻酸盐壳颗粒系统,用于口服胰岛素递送

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摘要

Oral administration of the drugs is considered as one of the most convenient and comfortable routes. However, an effective oral delivery of insulin still remains a challenging and elusive goal, due to bioavailability problem. The aim of our work is to develop a pH sensitive polymeric system for the oral delivery of insulin based on a poly (e-caprolactone) (PCL) core and shells of chitosan (CS) and alginate (ALG). The particles were prepared based on the double emulsion (water/oil/water) solvent evaporation method. The effect of blending Pluronic127 (F127) into the hydrophobic PCL matrix to improve its water permeability by increasing specific surface area. ALG have been chosen to provide the needed pH-sensitivity to the system. However, to coat the PCL surface with this anionic ALG layer a cationic CS layer has been added. The influence of each of the CS and ALG layers on the nanoparticle’s physiochemical properties as well as on the encapsulation efficiency and the drug release behavior of the nanoparticles was investigated. The results showed that CS and ALG shells increased the stability of the nanoparticles. The in vitro release studies using two different pH environments (1.2 and 6.8) to simulate the physiological conditions in the gastrointestinal tract (GIT) showed that, the particles have pH-responsive release patterns. The kinetics studies showed that, the insulin release from all the particles formulations obey the Korsmeyer-Peppas kinetic model.
机译:口服药物被认为是最方便,最舒适的路线之一。但是,由于生物利用度问题,有效的口服胰岛素仍然仍然是一个具有挑战性和难以捉摸的目标。我们工作的目的是开发一个pH敏感的聚合物系统,用于基于聚(E-Caprolactone)(PCL)核心和壳聚糖(CS)(CS)和藻酸盐(ALG)壳的胰岛素递送。根据双重乳液(水/油/水)溶剂蒸发法制备颗粒。将Pluronic127(F127)混合到疏水性PCL基质中的影响,通过增加特定表面积来改善其水的渗透性。已选择ALG为系统提供所需的pH值。但是,要用该阴离子ALG层覆盖PCL表面,已经添加了阳离子CS层。研究了每个CS和ALG层对纳米颗粒的生理化学特性以及封装效率和纳米颗粒的药物释放行为的影响。结果表明,CS和ALG壳增加了纳米颗粒的稳定性。使用两个不同的pH环境(1.2和6.8)模拟胃肠道(GIT)的生理条件的体外释放研究表明,颗粒具有pH响应性释放模式。动力学研究表明,胰岛素从所有颗粒制剂中释放出遵守Korsmeyer-Peppas动力学模型。

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