Department of Pharmacology, Post Graduate Institute of Medical Education & Research (PGIMER), Chandigarh 160012, India.
Department of Pharmaceutics, University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh, Punjab, India.
Int J Biol Macromol. 2024 Oct;277(Pt 1):133984. doi: 10.1016/j.ijbiomac.2024.133984. Epub 2024 Jul 23.
Small interfering RNA (siRNA) holds promise as a therapeutic approach for various diseases, yet challenges persist in achieving efficient delivery, biodistribution, and minimizing off-target effects. Lipidic nanoformulations are being developed to address these hurdles, but the optimal dose for preclinical investigations remains unclear. This systematic review and meta-analysis aims to determine the optimal dose of nanoformulated siRNA and explore factors influencing dose and biodistribution, informing future research in this field. A comprehensive search across four electronic databases identified 25 potential studies, with 15 selected for meta-analysis after screening. Quality assessment was conducted using SYRCLE's risk of bias tool modified for animal studies based on research question. Study found an average siRNA dose of 1.513 ± 0.377 mg/kg with mean downregulation of 65.79 % achieved, with siRNA-LNPs mainly accumulating in the liver. While individual factors showed no significant correlation, a positive association between dose and downregulation was observed, alongside other influencing factors. Extrapolating intravenous doses to potential oral doses, we suggest an initial oral dose range of 1.5 to 8 mg/kg, considering siRNA-LNPs bioavailability. These findings contribute to advancing RNA interference research and encourage further exploration of siRNA-based treatments in personalized medicine.
小干扰 RNA(siRNA)作为治疗各种疾病的一种有前途的方法,然而在实现高效传递、生物分布和最小化脱靶效应方面仍然存在挑战。正在开发脂质纳米制剂来解决这些难题,但用于临床前研究的最佳剂量仍不清楚。本系统评价和荟萃分析旨在确定纳米配方 siRNA 的最佳剂量,并探讨影响剂量和生物分布的因素,为该领域的未来研究提供信息。通过对四个电子数据库进行全面搜索,确定了 25 项潜在研究,经过筛选后,有 15 项被纳入荟萃分析。使用基于研究问题的 SYRCLE 风险偏倚工具对动物研究进行了修改,对质量进行了评估。研究发现,siRNA 的平均剂量为 1.513±0.377mg/kg,平均下调率为 65.79%,siRNA-LNPs 主要在肝脏中积累。虽然个别因素没有显示出显著相关性,但观察到剂量与下调之间存在正相关,以及其他影响因素。将静脉内剂量外推到潜在的口服剂量,我们建议考虑到 siRNA-LNPs 的生物利用度,初始口服剂量范围为 1.5 至 8mg/kg。这些发现有助于推进 RNA 干扰研究,并鼓励进一步探索基于 siRNA 的个性化医疗治疗方法。