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非病毒纳米药物用于核酸递送的细胞内加工:机制与方法。

On the cellular processing of non-viral nanomedicines for nucleic acid delivery: mechanisms and methods.

机构信息

Laboratory of General Biochemistry and Physical Pharmacy, Ghent University, Harelbekestraat 72, B-9000 Ghent, Belgium.

出版信息

J Control Release. 2012 Jul 20;161(2):566-81. doi: 10.1016/j.jconrel.2012.05.020. Epub 2012 May 18.

Abstract

In the field of nanomedicine, ample attention has been paid to the development of nanocarriers for the intracellular delivery of therapeutic cargo, such as nucleic acids for gene therapy. The efficiency with which these non-viral carriers deliver their payload at the required intracellular site of action remains low. Despite extensive research on cellular attachment, endocytosis and intracellular trafficking of nanocarriers, clear-cut rules for the design of effective nanocarriers to improve nucleic acid transfer are still lacking. This is mainly caused by the cell type-dependence of this highly dynamic cellular processing, and to the lack of reliable methods to study these events. For these reasons there is a strong demand for the development and standardization of such methods in order to better understand the intracellular dynamics of nanomedicine processing and validate cellular and intracellular targeting strategies. This review aims at providing an overview of the different processes that are currently known to be involved in the cellular processing of nanomedicines, with a focus on cellular internalization mechanisms, as this has received a great deal of attention in the last couple of years. Furthermore, the intracellular hurdles that need to be overcome to allow efficient NA transfer will be critically discussed. In addition, an overview will be given of various methodologies that have been applied to unravel these cellular processing mechanisms, with a discussion on their strengths and weaknesses.

摘要

在纳米医学领域,人们对纳米载体的开发给予了充分关注,这些纳米载体可用于将治疗性货物(如用于基因治疗的核酸)递送至细胞内。这些非病毒载体将其有效载荷递送至所需的细胞内作用部位的效率仍然较低。尽管对纳米载体的细胞附着、内吞作用和细胞内转运进行了广泛研究,但设计有效纳米载体以提高核酸传递效率的明确规则仍然缺乏。这主要是由于这种高度动态的细胞处理过程对细胞类型的依赖性,以及缺乏可靠的方法来研究这些事件。出于这些原因,强烈需要开发和标准化这些方法,以便更好地了解纳米医学处理的细胞内动力学,并验证细胞和细胞内靶向策略。本文综述了目前已知的纳米药物细胞处理过程中的不同过程,重点介绍了细胞内化机制,因为近年来人们对这一机制给予了极大的关注。此外,还将批判性地讨论克服这些细胞内障碍以允许有效 NA 转移所需的条件。此外,还将概述已应用于揭示这些细胞处理机制的各种方法,并讨论其优缺点。

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