目前正在进行的非病毒性siRNA疗法的临床试验
Eshan A Narasipura1, Rachel VanKeulen-Miller2, Yutian Ma1
1Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
Bioconjugate chemistry
|July 11, 2023
概括
短干扰RNA (siRNA) 在临床使用中面临交付挑战. 本综述涵盖了非病毒传递策略的创新,并总结了正在进行的siRNA临床试验.
科学领域:
- 生物技术和遗传医学 生物技术和遗传医学
- 药物输送系统 药物输送系统
- 临床试验 研究 研究 临床试验 临床试验
背景情况:
- 短干扰RNA (siRNA) 疗法表现有前途,但在体内*交付方面面临重大障碍.
- 低于最佳的传递特性是siRNA基基因药物的临床转化的主要障碍.
研究的目的:
- 为正在进行的siRNA临床试验提供临床专注的概述.
- 总结关于siRNA疗法的非病毒传递策略的创新.
- 突出有效的*in vivo*非病毒siRNA传递的关键挑战和策略.
主要方法:
- 关于siRNA传递障碍和生理化学性质的当前文献的综述.
- 分析特定的非病毒传递策略:序列修改,联体结合,纳米粒子和外体包装.
- 目前正在进行的siRNA临床试验的汇编和摘要,包括指示,目标和NCT号码.
主要成果:
- 确定了siRNA的关键*in vivo*传递障碍.
- 详细介绍了各种非病毒传递策略,以提高siRNA的疗效和控制.
- 介绍了当前siRNA临床试验的综合表.
结论:
- 有效的非病毒传递策略对于推进siRNA疗法至关重要.
- 目前正在进行的临床试验证明了siRNA技术的日益增长的潜力和应用.
- 进一步的交付创新对于克服广泛的siRNA临床使用所面临的挑战至关重要.
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