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通过高载量功能核酸的框架引导组装来制备脂质体。

Preparing liposomes through frame guided assembly with high-loading functional nucleic acids.

机构信息

CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, 100190, Beijing, China.

University of Chinese Academy of Sciences, 100049, Beijing, China.

出版信息

Nanoscale. 2023 Jun 15;15(23):9946-9953. doi: 10.1039/d3nr01412f.

Abstract

Recently, a frame guided assembly (FGA) has been demonstrated as a robust tool to prepare liposomes with customized morphologies. However, the potential application of FGA liposomes in delivering nucleic acid drugs is still limited by the low payload. In this study, by systemically investigating the correlation between the leading hydrophobic group (LHG) density and the initial detergent concentration, it has been demonstrated that frames with a low LHG density, which may facilitate the increase of the load of the nucleic acid drug, could be guided to form liposomes at low initial detergent concentrations. By capitalizing on this phenomenon, FGA liposomes with a high loading of ASO/siRNA have been successfully prepared and applied to treat pathogenic genes.

摘要

最近,框架引导组装(FGA)已被证明是一种强大的工具,可以制备具有定制形态的脂质体。然而,FGA 脂质体在递送核酸药物方面的潜在应用仍然受到载药量低的限制。在这项研究中,通过系统地研究先导疏水区(LHG)密度与初始去污剂浓度之间的相关性,证明了具有低 LHG 密度的框架可能更容易增加核酸药物的载药量,可以在低初始去污剂浓度下引导形成脂质体。利用这一现象,成功制备了载药量高的 ASO/siRNA 的 FGA 脂质体,并应用于治疗致病基因。

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