Extracellular vesicles-based drug delivery system for cancer treatment

Banuja Balachandran, Y. Yuana
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引用次数: 41

Abstract

Abstract The decrease in cancer mortality indicates an improvement in cancer treatment and management. One strategy that has been a focus in cancer treatment is development of drug delivery systems (DDS). Lipid-based nanoparticles (e.g. liposomes or micelles) has been used in current DDS as vehicles to transport active molecules. Extracellular vesicles (EVs), a new player in DDS, consist of lipid and thus, can be categorized as lipid-based nanoparticles. EVs are derived from cells and harbour various targeting molecules from their origin cells. Therefore, EVs are not foreign to the host immune system and may be more effective and efficient than other synthetic nanoparticles to target solid tumours with a minimum adverse effect, providing an exciting alternative for lipid-based DDS. Active molecules can be loaded into EV endogenously by exposing cells with active molecules to generate EVs carrying these molecules, or exogenous loading using physical or chemical methods. In this review, we summarise the recent developments of EV-based DDS where the choice of donor cells, drug cargo, loading methods, and administration routes are discussed. Further, consideration of the bioavailability and biodistribution of EVs, as well as current challenges concerning the potential biosafety issue and standardized up-scale production of EVs are highlighted.
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基于细胞外囊泡的肿瘤药物输送系统
癌症死亡率的下降表明癌症治疗和管理的改善。药物输送系统(DDS)的发展一直是癌症治疗的一个重点。基于脂质的纳米颗粒(如脂质体或胶束)已被用于当前的DDS作为运输活性分子的载体。细胞外囊泡(EVs)是DDS中的一个新参与者,它由脂质组成,因此可以归类为基于脂质的纳米颗粒。电动汽车来源于细胞,并含有来自其原始细胞的各种靶向分子。因此,ev对宿主免疫系统并不是外来的,并且可能比其他合成纳米颗粒更有效和高效地靶向实体肿瘤,副作用最小,为基于脂质的DDS提供了令人兴奋的替代方案。活性分子可以内源性加载到EV中,通过暴露具有活性分子的细胞来产生携带这些分子的EV,或者通过物理或化学方法外源性加载。在这篇综述中,我们总结了基于ev的DDS的最新进展,其中讨论了供体细胞的选择,药物货物,装载方法和给药途径。此外,还强调了电动汽车的生物利用度和生物分布,以及潜在的生物安全问题和标准化规模化生产等当前挑战。
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