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靶向细胞外囊泡递药系统采用超顺磁性氧化铁纳米粒子。

Targeted extracellular vesicle delivery systems employing superparamagnetic iron oxide nanoparticles.

机构信息

Department of Gastroenterology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China; School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, China.

Department of Hematology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China.

出版信息

Acta Biomater. 2021 Oct 15;134:13-31. doi: 10.1016/j.actbio.2021.07.027. Epub 2021 Jul 18.

Abstract

In the past decade, the study of extracellular vesicles (EVs), especially exosomes (50-150 nm) have attracted growing interest in numerous areas of cancer and tissue regeneration due to their unique biological features. A low isolation yield and insufficient targeting abilities limit their therapeutic applicability. Recently, superparamagnetic iron oxide nanoparticles (SPIONs) with magnetic navigation have been exploited to enhance the targeting ability of EVs. To construct targeted EV delivery systems engineered by SPIONs, several groups have pioneered the use of different techniques, such as electroporation, natural incubation, and cell extrusion, to directly internalize SPIONs into EVs. Furthermore, some endogenous ligands, such as transferrins, antibodies, aptamers, and streptavidin, were shown to enable modification of SPIONs, which increases binding with EVs. In this review, we summarized recent advances in targeted EV delivery systems engineered by SPIONs and focused on the key methodological approaches and the current applications of magnetic EVs. This report aims to address the existing challenges and provide comprehensive insights into targeted EV delivery systems. STATEMENT OF SIGNIFICANCE: Targeted extracellular vesicle (EV) delivery systems engineered by superparamagnetic iron oxide nanoparticles (SPIONs) have attracted wide attention and research interest in recent years. Such strategies employ external magnet fields to manipulate SPION-functionalized EVs remotely, aiming to enhance their accumulation and penetration in vivo. Although iron oxide nanoparticle laden EVs are interesting, they are controversial at present, hampering the progress in their clinical application. A thorough integration of these studies is needed for an advanced insight and rational design of targeted EV delivery systems. In this review, we summarize the latest advances in the design strategies of targeted EV delivery systems engineered by SPIONs with a focus on their key methodological approaches, current applications, limitation and future perspectives, which may facilitate the development of natural theranostic nanoplatforms.

摘要

在过去的十年中,由于其独特的生物学特性,细胞外囊泡(EVs),特别是外泌体(50-150nm)的研究在癌症和组织再生的众多领域引起了越来越多的关注。低分离产量和不足的靶向能力限制了它们的治疗适用性。最近,具有磁导航的超顺磁性氧化铁纳米粒子(SPIONs)已被用于增强 EV 的靶向能力。为了构建由 SPIONs 工程化的靶向 EV 递药系统,一些研究小组率先使用了不同的技术,如电穿孔、自然孵育和细胞挤压,将 SPIONs 直接内化到 EV 中。此外,一些内源性配体,如转铁蛋白、抗体、适体和链霉亲和素,被证明可以修饰 SPIONs,从而增加与 EV 的结合。在这篇综述中,我们总结了由 SPIONs 工程化的靶向 EV 递药系统的最新进展,并重点介绍了关键的方法学方法和磁性 EV 的当前应用。本报告旨在解决现有挑战,并对靶向 EV 递药系统提供全面的见解。

意义陈述

由超顺磁性氧化铁纳米粒子(SPIONs)工程化的靶向细胞外囊泡(EV)递药系统近年来引起了广泛关注和研究兴趣。这些策略利用外部磁场远程操纵 SPION 功能化的 EV,旨在增强其在体内的积累和渗透。虽然氧化铁纳米颗粒负载的 EV 很有趣,但目前它们存在争议,阻碍了它们在临床应用中的进展。需要对这些研究进行深入整合,以深入了解和合理设计靶向 EV 递药系统。在这篇综述中,我们总结了由 SPIONs 工程化的靶向 EV 递药系统的最新设计策略,重点介绍了其关键方法学方法、当前应用、局限性和未来展望,这可能有助于天然治疗性纳米平台的发展。

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