Suppr超能文献

外泌体作为仿生纳米载体用于 RNA 递送:制备与应用。

Exosomes as bio-inspired nanocarriers for RNA delivery: preparation and applications.

机构信息

Faculty of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

J Transl Med. 2022 Mar 14;20(1):125. doi: 10.1186/s12967-022-03325-7.

Abstract

Nanocarriers as drug/biomolecule delivery systems have been significantly developed during recent decades. Given the stability, reasonable delivery efficiency, and safety of nanocarriers, there are several barriers in the fulfillment of successful clinical application of these delivery systems. These challenges encouraged drug delivery researchers to establish innovative nanocarriers with longer circulation time, high stability, and high compatibility. Exosomes are extracellular nanometer-sized vesicles released through various cells. These vesicles serve as nanocarriers, possessing great potential to overcome some obstacles encountered in gene and drug delivery due to their natural affinity to recipient cells and the inherent capability to shuttle the genes, lipids, proteins, and RNAs between cells. So far, there has been a lot of valuable research on drug delivery by exosomes, but research on RNA delivery, especially mRNA, is very limited. Since mRNA-based vaccines and therapies have recently gained particular prominence in various diseases, it is essential to find a suitable delivery system due to the large size and destructive nature of these nucleic acids. That's why we're going to take a look at the unique features of exosomes and their isolation and loading methods, to embrace this idea that exosome-mediated mRNA-based therapies would be introduced as a very efficient strategy in disease treatment within the near future.

摘要

在过去的几十年中,作为药物/生物分子传递系统的纳米载体得到了极大的发展。鉴于纳米载体的稳定性、合理的传递效率和安全性,这些传递系统要成功应用于临床还存在一些障碍。这些挑战促使药物输送研究人员开发出具有更长循环时间、更高稳定性和更高兼容性的创新型纳米载体。外泌体是通过各种细胞释放的纳米尺寸的细胞外囊泡。这些囊泡作为纳米载体,由于其与受体细胞的天然亲和力以及在细胞间穿梭基因、脂质、蛋白质和 RNA 的固有能力,具有克服基因和药物传递中遇到的一些障碍的巨大潜力。到目前为止,已经有很多关于外泌体药物传递的有价值的研究,但关于 RNA 传递的研究,特别是 mRNA 的研究非常有限。由于基于 mRNA 的疫苗和疗法最近在各种疾病中引起了特别的关注,由于这些核酸的体积大和破坏性,因此需要找到合适的传递系统。这就是为什么我们要研究外泌体的独特特征及其分离和加载方法,以接受外泌体介导的基于 mRNA 的治疗将作为一种非常有效的策略,在不久的将来引入疾病治疗的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7256/8919646/51ba5bb37ae8/12967_2022_3325_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验