细胞膜包覆的纳米药物在肿瘤治疗中的研究进展
Research progress of cell membrane-coated nanoparticles in tumor therapy
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摘要: 传统的化疗手段缺乏肿瘤靶向性, 且会造成明显的全身毒副反应。纳米药物递送系统开启了癌症精准治疗的新篇章, 由于肿瘤内血管异常造成的增强渗透滞留效应, 纳米药物被动地靶向肿瘤组织。然而, 大多数纳米颗粒被单核吞噬系统迅速清除, 限制了其抗肿瘤疗效。近年来, 细胞膜纳米药物(cell membrane-coated nanoparticles, CNPs) 在肿瘤治疗方面展现出广阔的应用潜力。CNPs是被细胞膜包裹的纳米药物颗粒, 不仅具有良好的生物相容性, 还能保留原细胞膜的生物特性: 红细胞膜CNPs能延长药物体内循环时间; 血小板膜CNPs、免疫细胞膜CNPs、干细胞膜CNPs均表现出趋向肿瘤的能力, 免疫细胞膜CNPs还能调节抗肿瘤免疫; 肿瘤细胞膜CNPs因其良好的同源靶向性得到广泛研究。本文概述了CNPs的构建过程, 分别介绍了基于各类细胞膜的CNPs在肿瘤治疗中的作用, 并讨论了其未来应用前景和挑战。Abstract: Traditional chemotherapy methods lack tumor targeting and cause obvious systemic adverse reactions. The development of nano-drug particles delivery systems has ushered in a new chapter in precision tumor treatment. Due to the enhanced permeability and retention (EPR) effect caused by anomalous tumor blood vessels, nanoparticles can passively target tumor tissues. However, most nanoparticles are rapidly cleared by the mononuclear phagocytic system, limiting their anti-tumor efficacy. In recent years, cell membrane-coated nanoparticles (CNPs) have shown great potential for application in tumor therapy. CNPs are nano-drug particles wrapped by cell membranes, which can not only exhibit excellent biocompatibility, but also retain some of the biological characteristics of the original cell membrane. CNPs from erythrocyte can extend the blood circulation duration of drugs. CNPs from platelet, CNPs from immunocyte, and CNPs from stem cell all demonstrate a tumor-targeting capability, CNPs from immunocyte can also regulate anti-tumor immunity. CNPs from tumor cell have been extensively researched for their excellent homogenous targeting properties. In this review, we outline the construction process of CNPs, and introduce the roles of CNPs based on various cell membranes in tumor therapy, and discuss their future application prospects and challenges.
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