间充质干细胞衍生的细胞外囊泡:最新疗法和靶向给药进展

Anjali Bhat, Anshu Malik, Poonam Yadav, Wend-Pingda Jessica Ware, Pratiksha Kakalij, Subhash Chand
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引用次数: 0

摘要

靶向给药领域正在迅速发展,其重点是开发生物相容性纳米粒子,以满足无毒性、生物相容性和有效释放封装分子的严格标准。传统的合成纳米粒子(SNPs)面临着免疫反应升高、合成方法复杂和毒性等复杂问题,限制了它们在治疗和药物输送方面的应用。细胞外囊泡(EVs)凭借其穿越生物屏障的能力、生物相容性、低毒性和天然来源,已成为有前途的 SNP 替代品。值得注意的是,间充质干细胞衍生的EVs(间充质干细胞-EVs)因其在治疗和药物递送方面的潜力而备受关注。研究表明,间充质干细胞-EVs是间充质干细胞的核心旁分泌物,可复制间充质干细胞的治疗效果。这篇综述探讨了间充质干细胞-EV 的特点,强调了它们在治疗和药物输送方面的潜力,包括用于基因编辑的 CRISPR/Cas9 输送。它还深入探讨了间充质干细胞-EV 在临床应用中遇到的障碍和挑战,并对克服生物分布和靶向递送限制的策略提出了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mesenchymal stem cell-derived extracellular vesicles: Recent therapeutics and targeted drug delivery advances

Mesenchymal stem cell-derived extracellular vesicles: Recent therapeutics and targeted drug delivery advances

The targeted drug delivery field is rapidly advancing, focusing on developing biocompatible nanoparticles that meet rigorous criteria of non-toxicity, biocompatibility, and efficient release of encapsulated molecules. Conventional synthetic nanoparticles (SNPs) face complications such as elevated immune responses, complex synthesis methods, and toxicity, which restrict their utility in therapeutics and drug delivery. Extracellular vesicles (EVs) have emerged as promising substitutes for SNPs, leveraging their ability to cross biological barriers, biocompatibility, reduced toxicity, and natural origin. Notably, mesenchymal stem cell-derived EVs (MSC-EVs) have garnered much curiosity due to their potential in therapeutics and drug delivery. Studies suggest that MSC-EVs, the central paracrine contributors of MSCs, replicate the therapeutic effects of MSCs. This review explores the characteristics of MSC-EVs, emphasizing their potential in therapeutics and drug delivery for various diseases, including CRISPR/Cas9 delivery for gene editing. It also delves into the obstacles and challenges of MSC-EVs in clinical applications and provides insights into strategies to overcome the limitations of biodistribution and target delivery.

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