Clinical Trials of Functional Nucleic Acids

Martina Traykovska, Sjoerd Miedema, Robert Penchovsky
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引用次数: 5

Abstract

This chapter describes how functional nucleic acids, such as aptamers, antisense oligonucleotides (ASOs), small interfering (si) RNAs, and ribozymes are considered by some researchers as valuable tools to develop therapeutic agents. They have not been particularly fast in reaching the market as medicines, due to endogenous barriers to extracellular trafficking and cellular uptake of nucleic acids and their inherent instability when applied in vivo. However, research carried out by the nucleic acid engineering community and pharmaceutical companies to circumvent these obstacles has led to the approval of a few aptamers and ASOs as drugs. Nucleic acid therapeutics are usually administered locally to diseased tissue. The drug candidates currently in clinical trials commonly use the same administration methods as previously licensed nucleic acid therapeutics. These administration techniques carry their own safety risks and advantages. In this article, the present state is discussed and prospective options for the use ASOs and aptamers as drugs are listed.
功能性核酸的临床试验
本章描述了功能性核酸,如适体、反义寡核苷酸(ASOs)、小干扰rna (si)和核酶是如何被一些研究人员认为是开发治疗剂的有价值的工具。由于细胞外运输和细胞摄取核酸的内源性障碍以及它们在体内应用时固有的不稳定性,它们作为药物进入市场的速度不是特别快。然而,核酸工程界和制药公司为规避这些障碍而进行的研究已经导致一些适体和aso被批准为药物。核酸疗法通常是局部施用于病变组织。目前处于临床试验中的候选药物通常使用与先前许可的核酸治疗相同的给药方法。这些管理技术有其自身的安全风险和优势。在本文中,讨论了目前的状态,并列出了使用ASOs和适配体作为药物的未来选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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