提高核酸基纳米材料稳定性的方法。

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xueping Xie, Wenjuan Ma, Yuxi Zhan, Qifeng Zhang, Chaowei Wang, Huiyong Zhu
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引用次数: 0

摘要

核酸链可以通过严格的碱基配对合成各种基于核酸的纳米材料(NANs)。自组装纳米材料具有可编程性、智能性、生物相容性、非免疫原性和非细胞毒性。随着纳米技术的快速发展,纳米材料在药物递送、生物传感等生物医学领域的应用受到了广泛关注。然而,纳米材料的稳定性通常受到阳离子浓度、酶降解和有机溶剂的影响。这种易降解性是限制纳米材料应用的最重要因素之一。NANs可以在低阳离子浓度、酶存在和有机溶剂的条件下变性或降解。为了解决这个问题,人们尝试了许多方法来提高纳米材料的稳定性,包括人工核酸、用特定基团修饰、用保护结构封装等。在这篇综述中,我们总结了相关方法,以更深入地了解纳米材料的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methods to Improve the Stability of Nucleic Acid-Based Nanomaterials.

Nucleic acid strands can be synthesized into various nucleic acid-based nanomaterials (NANs) through strict base pairing. The self-assembled NANs are programmable, intelligent, biocompatible, non-immunogenic, and non-cytotoxic. With the rapid development of nanotechnology, the application of NANs in the biomedical fields, such as drug delivery and biological sensing, has attracted wide attention. However, the stability of NANs is often affected by the cation concentrations, enzymatic degradation, and organic solvents. This susceptibility to degradation is one of the most important factors that have restricted the application of NANs. NANs can be denatured or degraded under conditions of low cation concentrations, enzymatic presence, and organic solvents. To deal with this issue, a lot of methods have been attempted to improve the stability of NANs, including artificial nucleic acids, modification with specific groups, encapsulation with protective structures, etc. In this review, we summarized the relevant methods to have a deeper understanding of the stability of NANs.

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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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