Gatto Matthew S, Johnson McNeely P, Najahi-Missaoui Wided
Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602, USA.
Life (Basel). 2024 May 24;14(6):672. doi: 10.3390/life14060672.
In drug development, it is not uncommon that an active substance exhibits efficacy in vitro but lacks the ability to specifically reach its target in vivo. As a result, targeted drug delivery has become a primary focus in the pharmaceutical sciences. Since the approval of Doxil in 1995, liposomes have emerged as a leading nanoparticle in targeted drug delivery. Their low immunogenicity, high versatility, and well-documented efficacy have led to their clinical use against a wide variety of diseases. That being said, every disease is accompanied by a unique set of physiological conditions, and each liposomal product must be formulated with this consideration. There are a multitude of different targeting techniques for liposomes that can be employed depending on the application. Passive techniques such as PEGylation or the enhanced permeation and retention effect can improve general pharmacokinetics, while active techniques such as conjugating targeting molecules to the liposome surface may bring even further specificity. This review aims to summarize the current strategies for targeted liposomes in the treatment of diseases.
在药物研发过程中,活性物质在体外显示出疗效但在体内缺乏特异性到达靶点的能力,这种情况并不罕见。因此,靶向给药已成为药学领域的主要研究重点。自1995年多柔比星脂质体(Doxil)获批以来,脂质体已成为靶向给药领域的领先纳米颗粒。其低免疫原性、高通用性以及充分记录的疗效使其被用于治疗多种疾病。话虽如此,每种疾病都伴随着一组独特的生理条件,每种脂质体产品在配方时都必须考虑到这一点。根据应用的不同,可以采用多种不同的脂质体靶向技术。诸如聚乙二醇化或增强渗透与滞留效应等被动技术可以改善一般药代动力学,而诸如将靶向分子偶联到脂质体表面等主动技术可能会带来更高特异性。本综述旨在总结目前靶向脂质体治疗疾病的策略。