通过将nt-PE附着在表面,提高海藻酸-壳聚糖纳米颗粒通过上皮的运输效率

RAN Pub Date : 2016-04-01 DOI:10.11159/NDDTE16.111
Ruiying Li, P. D. Bank, R. Mrsny
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引用次数: 1

摘要

纳米技术将给药系统带入了一个崭新的时代——纳米给药系统的出现。它在不同的治疗领域得到了广泛的探索。对于口服蛋白质递送,纳米递送系统在小肠上皮内的运输效率较低,限制了其应用。纳米递送系统通过上皮的有效运输需要优化表面特性和特定的运输途径。本研究选择壳聚糖和海藻酸盐制备纳米颗粒,因为它们具有生物粘附性、可生物降解性,并且可以进行表面修饰。纳米颗粒穿过上皮的途径被设计成模拟病毒在体内的入侵途径。研究表明,无毒形式的假单胞菌外毒素(nt-PE)可以穿过极化细胞(上皮细胞)[1]。我们的假设是海藻酸-壳聚糖纳米颗粒在将nt-PE附着在上皮表面后可以提高其通过上皮的运输效率。采用离子凝胶法制备了海藻酸盐-壳聚糖纳米颗粒,粒径范围为210±18 nm, zeta电位为-7±3 mV。将nt-PE吸附在纳米颗粒表面后,纳米颗粒的尺寸范围为192±17 nm, zeta电位为-10±4 mV。在透射电子显微镜下,Nt-PE修饰的纳米颗粒仍呈球形。该纳米递送系统在体外人肠上皮模型Caco-2细胞上进行了测试。纳米粒子的输运效率是未修饰纳米粒子的2倍。Nt-PE修饰的纳米颗粒已显示出跨越上皮的潜力。体内转运研究正在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increase alginate-chitosan nanoparticles transport efficiency through the epithelium by attaching nt-PE onto surface
Extended Abstract Nanotechnology has brought drug delivery system into a brand new age---the appearance of Nano delivery system. It has been widely explored in different therapeutic areas. For oral protein delivery, the application of Nano delivery system is limited by the low transport efficiency through the epithelium in the small intestine. The efficient transport of nano delivery system through epithelium requires optimized surface characteristics and specific transport pathway. In this study, chitosan and alginate are chosen for making nanoparticles, as they are bioadhensive, biodegradable and can be modified for the surface modification. The pathway of nanoparticles go across the epithelium is designed to mimic the pathway of virus invasion in the body. Study has shown non-toxic form of pseudomonas exotoxin (nt-PE) can go across the polarized cells (epithelial cells) [1]. Our hypothesis is that the transport efficiency of alginate-chitosan nanoparticles through the epithelium can be increased after attaching nt-PE onto the surface. Alginate-chitosan nanoparticles were made by ion gelation, the particle size are in the size range of 210± 18 nm and the zeta potential is -7±3 mV. After attaching nt-PE onto nanoparticle surface, nanoparticles are in the size range of 192±17 nm, and the zeta potential is -10±4 mV. Nt-PE decorated nanoparticles are still in the spherical shape as indicated under Transmission Electron Microscope. This nano-delivery system was tested on Caco-2 cells, an in vitro model of the human intestinal epithelium. The transport efficiency of nt-PE modified nanoparticles are 2 fold more than the unmodified nanoparticles. Nt-PE modified nanoparticles have shown the potential to go across the epithelium. The in vivo transport study is undergoing.
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