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信使核糖核酸递送系统中的交互设计。

Interaction design in mRNA delivery systems.

作者信息

Yu Mengyao, Lin Lixin, Zhou Dezhong, Liu Shuai

机构信息

College of Pharmaceutical Sciences, State Key Laboratory of Advanced Drug Delivery and Release Systems, Zhejiang University, Hangzhou 310058, China; Liangzhu Laboratory, Zhejiang University, Hangzhou 311121, China.

School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, China.

出版信息

J Control Release. 2025 Jan 10;377:413-426. doi: 10.1016/j.jconrel.2024.11.038. Epub 2024 Nov 26.

Abstract

Following the coronavirus disease 2019 (COVID-19) pandemic, mRNA technology has made significant breakthroughs, emerging as a potential universal platform for combating various diseases. To address the challenges associated with mRNA delivery, such as instability and limited delivery efficacy, continuous advancements in genetic engineering and nanotechnology have led to the exploration and refinement of various mRNA structural modifications and delivery platforms. These achievements have significantly broadened the clinical applications of mRNA therapies. Despite the progress, the understanding of the interactions in mRNA delivery systems remains limited. These interactions are complex and multi-dimensional, occurring between mRNA and vehicles as well as delivery materials and helper ingredients. Resultantly, stability of the mRNA delivery systems and their delivery efficiency can be both significantly affected. This review outlines the current state of mRNA delivery strategies and summarizes the interactions in mRNA delivery systems. The interactions include the electrostatic interactions, hydrophobic interactions, hydrogen bonding, π-π stacking, coordination interactions, and so on. This interaction understanding provides guideline for future design of next-generation mRNA delivery systems, thereby offering new perspectives and strategies for developing diverse mRNA therapeutics.

摘要

在2019年冠状病毒病(COVID-19)大流行之后,mRNA技术取得了重大突破,成为对抗各种疾病的潜在通用平台。为应对与mRNA递送相关的挑战,如不稳定性和递送效率有限,基因工程和纳米技术的不断进步促使人们探索和优化各种mRNA结构修饰及递送平台。这些成果显著拓宽了mRNA疗法的临床应用。尽管取得了进展,但对mRNA递送系统中相互作用的理解仍然有限。这些相互作用复杂且具有多维度性,发生在mRNA与载体以及递送材料和辅助成分之间。因此,mRNA递送系统的稳定性及其递送效率都会受到显著影响。本综述概述了mRNA递送策略的现状,并总结了mRNA递送系统中的相互作用。这些相互作用包括静电相互作用、疏水相互作用、氢键、π-π堆积、配位相互作用等。这种对相互作用的理解为下一代mRNA递送系统的未来设计提供了指导,从而为开发多样化的mRNA疗法提供了新的视角和策略。

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