Department of Chemistry, College of Arts and Sciences, Washington State University, Pullman, WA 99164, USA.
Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602, USA.
Int J Mol Sci. 2023 Apr 1;24(7):6615. doi: 10.3390/ijms24076615.
Since their first discovery in the 1960s by Alec Bangham, liposomes have been shown to be effective drug delivery systems for treating various cancers. Several liposome-based formulations received approval by the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA), with many others in clinical trials. Liposomes have several advantages, including improved pharmacokinetic properties of the encapsulated drug, reduced systemic toxicity, extended circulation time, and targeted disposition in tumor sites due to the enhanced permeability and retention (EPR) mechanism. However, it is worth noting that despite their efficacy in treating various cancers, liposomes still have some potential toxicity and lack specific targeting and disposition. This explains, in part, why their translation into the clinic has progressed only incrementally, which poses the need for more research to focus on addressing such translational limitations. This review summarizes the main properties of liposomes, their current status in cancer therapy, and their limitations and challenges to achieving maximal therapeutic efficacy.
自 20 世纪 60 年代 Alec Bangham 首次发现以来,脂质体已被证明是治疗各种癌症的有效药物递送系统。几种基于脂质体的制剂已获得美国食品和药物管理局 (FDA) 和欧洲药品管理局 (EMA) 的批准,还有许多其他制剂正在临床试验中。脂质体具有多种优点,包括改善包裹药物的药代动力学特性、降低全身毒性、延长循环时间以及由于增强的通透性和保留 (EPR) 机制而在肿瘤部位的靶向分布。然而,值得注意的是,尽管脂质体在治疗各种癌症方面具有疗效,但它们仍然存在一些潜在的毒性,并且缺乏特异性靶向和分布。这部分解释了为什么它们向临床的转化进展缓慢,这就需要更多的研究来集中解决这些转化限制。本综述总结了脂质体的主要性质、它们在癌症治疗中的现状以及实现最大治疗效果的限制和挑战。