受细胞外囊泡启发的新型仿生药物递送纳米颗粒。

IF 8.2
Viswanathan Sundaram, Santosh Aryal
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引用次数: 0

摘要

纳米粒子(NPs)由细胞成分组成,如具有仿生前景的细胞外囊泡(EVs),已成为纳米医学领域的一种革命性方法,为靶向药物给药、免疫治疗、监测治疗反应和诊断应用提供了显著的益处。利用天然细胞膜、膜蛋白和细胞内容物的独特特性,这些仿生NPs从其来源和生物发生中获得必要的生物学功能,包括免疫逃避、延长循环和目标识别,使其成为治疗应用的最佳候选者。本文综述了电动汽车注入合成NP系统的方法的全面检查,以克服各自的缺点。例如,电动汽车具有生物源性,具有细胞靶向性,但其分离率有限,结构和胶体稳定性较弱。然而,我们在大规模生产高度稳定的合成NPs方面有几十年的经验,它们缺乏细胞靶向特性。因此,将这两个系统整合为一个单一的实体在纳米医学领域得到了极大的关注。在这篇综述中,我们强调了各种各样的EVs来源,如红细胞、白细胞、癌细胞和干细胞,每一种都提供独特的生物学益处。在解决可扩展性、膜稳定性和功能保存等问题的同时,研究了包括EV分离、涂层工艺和材料集成在内的关键程序。此外,还分析了它们在定制医疗方面的前景,重点介绍了它们的即时医疗应用。这篇综述旨在阐明现有的方法,它们的局限性,以及在创造ev衍生的用于临床的仿生NPs方面的前瞻性进展。这篇文章被分类为:生物学的纳米技术方法;生物学的纳米系统;治疗方法和药物发现;肿瘤疾病的纳米医学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging Biomimetic Drug Delivery Nanoparticles Inspired by Extracellular Vesicles.

Nanoparticles (NPs) made up of cellular components such as extracellular vesicles (EVs) with a biomimetic outlook have emerged as a revolutionary approach in nanomedicine, providing significant benefits for targeted drug administration, immunotherapy, monitoring therapeutic response, and diagnostic applications. Utilizing the distinctive characteristics of natural cell membranes, membrane proteins, and cellular contents, these biomimetic NPs acquire essential biological functions from their source and biogenesis, including immune evasion, extended circulation, and target recognition, rendering them optimal candidates for therapeutic applications. This review offers a comprehensive examination of the methodologies of EVs infused with synthetic NP systems with the goal of overcoming their respective shortcomings. For instance, EVs are biogenic with cellular targeting features, but their isolation yield is limited, and their structural and colloidal stability are weak. Whereas, we have decades of experience in the mass production of highly stable synthetic NPs, they lack cellular targeting features. Therefore, the integration of these two systems as a single entity in the field of nanomedicine has gained significant attention. In this review, we emphasized the variety of EVs sources, such as erythrocytes, leukocytes, cancer cells, and stem cells, each providing unique biological benefits. Critical procedures encompassing EV's separation, coating processes, and material integration were examined while addressing the issues, including scalability, membrane stability, and preservation of functionality. Additionally, their promise in customized medicine is analyzed, highlighting their immediate medical applications. This review seeks to elucidate the existing methodologies, their constraints, and prospective advancements in the creation of EV-derived biomimetic NPs for clinical use. This article is categorized under: Nanotechnology Approaches to Biology > Nanoscale Systems in Biology Therapeutic Approaches and Drug Discovery > Nanomedicine for Oncologic Disease.

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