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用于癌症靶向给药的聚合物基纳米颗粒的制造技术与表面工程

Manufacturing Techniques and Surface Engineering of Polymer Based Nanoparticles for Targeted Drug Delivery to Cancer.

作者信息

Wang Yichao, Li Puwang, Truong-Dinh Tran Thao, Zhang Juan, Kong Lingxue

机构信息

School of Electrical and Computer Engineering, RMIT University, Melbourne, VIC 3000, Australia.

Institute for Frontier Materials, Deakin University, Locked Bag 20000, Geelong, VIC 3220, Australia.

出版信息

Nanomaterials (Basel). 2016 Feb 1;6(2):26. doi: 10.3390/nano6020026.

Abstract

The evolution of polymer based nanoparticles as a drug delivery carrier via pharmaceutical nano/microencapsulation has greatly promoted the development of nano- and micro-medicine in the past few decades. Poly(lactide-co-glycolide) (PLGA) and chitosan, which are biodegradable and biocompatible polymers, have been approved by both the Food & Drug Administration (FDA) and European Medicine Agency (EMA), making them ideal biomaterials that can be advanced from laboratory development to clinical oral and parental administrations. PLGA and chitosan encapsulated nanoparticles (NPs) have successfully been developed as new oral drug delivery systems with demonstrated high efficacy. This review aims to provide a comprehensive overview of the fabrication of PLGA and chitosan particulate systems using nano/microencapsulation methods, the current progress and the future outlooks of the nanoparticulate drug delivery systems. Especially, we focus on the formulations and nano/micro-encapsulation techniques using top-down techniques. It also addresses how the different phases including the organic and aqueous ones in the emulsion system interact with each other and subsequently influence the properties of the drug delivery system. Besides, surface modification strategies which can effectively engineer intrinsic physicochemical properties are summarised. Finally, future perspectives and potential directions of PLGA and chitosan nano/microencapsulated drug systems are outlined.

摘要

在过去几十年中,通过药物纳米/微囊化将基于聚合物的纳米颗粒作为药物递送载体的发展极大地推动了纳米医学和微医学的发展。聚(丙交酯-共-乙交酯)(PLGA)和壳聚糖是可生物降解且具有生物相容性的聚合物,已获得美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)的批准,这使它们成为理想的生物材料,能够从实验室研发推进到临床口服和肠胃外给药。PLGA和壳聚糖包封的纳米颗粒(NPs)已成功开发为具有高疗效的新型口服药物递送系统。本综述旨在全面概述使用纳米/微囊化方法制备PLGA和壳聚糖颗粒系统、纳米颗粒药物递送系统的当前进展和未来展望。特别是,我们关注使用自上而下技术的制剂和纳米/微囊化技术。它还探讨了乳液系统中的有机相和水相在内的不同相如何相互作用,进而影响药物递送系统的性质。此外,总结了能够有效改变固有物理化学性质的表面改性策略。最后,概述了PLGA和壳聚糖纳米/微囊化药物系统的未来前景和潜在方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/add8/5302480/33a7e100a538/nanomaterials-06-00026-g001.jpg

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