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通过肺部途径控制蛋白质/肽的释放。

Controlling the release of proteins/peptides via the pulmonary route.

作者信息

Shoyele Sunday A

机构信息

University of Bradford, Bradford, UK.

出版信息

Methods Mol Biol. 2008;437:141-8. doi: 10.1007/978-1-59745-210-6_6.

Abstract

The inhalation route is seen as the most promising non-invasive alternative for the delivery of proteins; however, the short duration of activity of drugs delivered via this route brought about by the activities of alveolar macrophages and mucociliary clearance means there is a need to develop controlled release system to prolong the activities of proteins delivered to the lung. Polymeric materials such as (D,L)-poly(lactic glycolic acid) (PLGA), chitosan and poly(ethylene glycol) (PEGs) have been used for controlled release of proteins. Other systems such as liposomes and microcrystallization have also proved effective. This chapter gives a more detailed understanding of these techniques and the manufacture of the delivery systems.

摘要

吸入途径被视为递送蛋白质最具前景的非侵入性替代方法;然而,通过该途径递送的药物由于肺泡巨噬细胞的活性和黏液纤毛清除作用而导致活性持续时间较短,这意味着需要开发控释系统来延长递送至肺部的蛋白质的活性。诸如(D,L)-聚乳酸乙醇酸共聚物(PLGA)、壳聚糖和聚乙二醇(PEGs)等聚合材料已用于蛋白质的控释。其他系统如脂质体和微晶化也已证明是有效的。本章将更详细地介绍这些技术以及递送系统的制造。

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