Marqués-Gallego Patricia, de Kroon Anton I P M
Membrane Biochemistry & Biophysics, Bijvoet Center for Biomolecular Research and Institute of Biomembranes, Utrecht University, Padualaan 8, H.R. Kruyt Building, 3584 CH Utrecht, The Netherlands.
Biomed Res Int. 2014;2014:129458. doi: 10.1155/2014/129458. Epub 2014 Jul 14.
Liposomes have been exploited for pharmaceutical purposes, including diagnostic imaging and drug and gene delivery. The versatility of liposomes as drug carriers has been demonstrated by a variety of clinically approved formulations. Since liposomes were first reported, research of liposomal formulations has progressed to produce improved delivery systems. One example of this progress is stealth liposomes, so called because they are equipped with a PEGylated coating of the liposome bilayer, leading to prolonged blood circulation and improved biodistribution of the liposomal carrier. A growing research area focuses on the preparation of liposomes with the ability of targeting specific tissues. Several strategies to prepare liposomes with active targeting ligands have been developed over the last decades. Herein, several strategies for the functionalization of liposomes are concisely summarized, with emphasis on recently developed technologies for the covalent conjugation of targeting ligands to liposomes.
脂质体已被用于制药目的,包括诊断成像以及药物和基因递送。多种临床批准的制剂已证明脂质体作为药物载体的多功能性。自从首次报道脂质体以来,脂质体制剂的研究已取得进展,以生产出改进的递送系统。这一进展的一个例子是隐形脂质体,之所以这样称呼是因为它们在脂质体双层上配备了聚乙二醇化涂层,从而导致脂质体载体的血液循环时间延长和生物分布得到改善。一个不断发展的研究领域专注于制备具有靶向特定组织能力的脂质体。在过去几十年中,已经开发了几种制备带有活性靶向配体的脂质体的策略。在此,简要总结了脂质体功能化的几种策略,重点是最近开发的将靶向配体与脂质体共价结合的技术。