小干扰RNA
药理学
医学
药代动力学
生物利用度
核糖核酸
生物
基因
生物化学
作者
Ahmed Abosalha,Jacqueline L. Boyajian,Waqar Ahmad,Paromita Islam,Merry Ghebretatios,Sabrina Schaly,Rahul Thareja,Karan Arora,Satya Prakash
标识
DOI:10.1080/17512433.2022.2136166
摘要
Few siRNA-based products have been approved recently by the Food and Drug Administration (FDA) and other regulatory agencies after approximately 20 years following its discovery due to the associated limitations. The absorption, distribution, metabolism, and excretion of siRNA therapeutics are highly restricted by several obstacles, resulting in rapid clearance of siRNA-based therapeutic products from systemic circulation before reaching the cytosol of targeted cells. The siRNA therapeutics however are very promising in many diseases, including gene therapy and SARS-COV-2 viral infection. The design of suitable delivery vehicles and developing strategies toward better pharmacokinetic parameters may solve the challenges of siRNA therapies.
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