医学
基因沉默
小干扰RNA
生物信息学
药理学
药品
食品药品监督管理局
重症监护医学
生物
核糖核酸
生物化学
基因
作者
Puneetpal Singh,Monica Singh,Baani Singh,Kirti Sharma,Nitin Kumar,Deepinder Singh,Harpal Singh Klair,Sarabjit S. Mastana
出处
期刊:Biomedicines
[MDPI AG]
日期:2024-01-01
卷期号:12 (1): 90-90
标识
DOI:10.3390/biomedicines12010090
摘要
The global statistics of bone disorders, skeletal defects, and fractures are frightening. Several therapeutic strategies are being used to fix them; however, RNAi-based siRNA therapy is starting to prove to be a promising approach for the prevention of bone disorders because of its advanced capabilities to deliver siRNA or siRNA drug conjugate to the target tissue. Despite its ‘bench-to-bedside’ usefulness and approval by food and drug administration for five siRNA-based therapeutic medicines: Patisiran, Vutrisiran, Inclisiran, Lumasiran, and Givosiran, its use for the other diseases still remains to be resolved. By correcting the complications and complexities involved in siRNA delivery for its sustained release, better absorption, and toxicity-free activity, siRNA therapy can be harnessed as an experimental tool for the prevention of complex and undruggable diseases with a personalized medicine approach. The present review summarizes the findings of notable research to address the implications of siRNA in bone health for the restoration of bone mass, recovery of bone loss, and recuperation of bone fractures.
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