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优化用于基因治疗的纳米颗粒设计:保护寡核苷酸不被降解,同时不妨碍药物释放。

Optimizing Nanoparticle Design for Gene Therapy: Protection of Oligonucleotides from Degradation Without Impeding Release of Cargo.

作者信息

Fihurka Oksana, Sanchez-Ramos Juan, Sava Vasyl

机构信息

Department of Neurology College of Medicine, University of South Florida, Tampa, FL, USA.

出版信息

Nanomed Nanosci Res. 2018;2(6). doi: 10.29011/2577-1477.100055. Epub 2018 Nov 23.

Abstract

Gene therapy delivery systems that rely on synthetic nanocarriers can be optimized by assays of nucleic acid protection and kinetic studies of nucleic acid release. These empirical measurements ensure nanoparticle stability and predict potential efficacy. Quantitative methods for assessment of the capacity of nanoparticles to protect oligonucleotide cargo and to measure the rate of release of the cargo were developed and tested based on six commercial cationic matrices. study of drug release kinetics provides predictable release rates under a variety of conditions which can be adapted to appropriate physiological factors that affect release . In brief, DNA release and DNase I degradation assays described here will be useful for optimization of nanocarrier-mediated gene therapy administration by various routes.

摘要

依赖合成纳米载体的基因治疗递送系统可通过核酸保护测定和核酸释放动力学研究来优化。这些实证测量可确保纳米颗粒的稳定性并预测潜在疗效。基于六种商业阳离子基质,开发并测试了评估纳米颗粒保护寡核苷酸货物能力以及测量货物释放速率的定量方法。药物释放动力学研究提供了在各种条件下可预测的释放速率,这些条件可适应影响释放的适当生理因素。简而言之,本文所述的DNA释放和DNase I降解测定对于通过各种途径优化纳米载体介导的基因治疗给药将是有用的。

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