Exploring dose and downregulation dynamics in lipid nanoparticles based siRNA therapy: Systematic review and meta-analysis

被引:1
作者
Kumar, Anil [1 ]
Ahmed, Bakr [2 ]
Kaur, Indu Pal [2 ]
Saha, Lekha [1 ]
机构
[1] Post Grad Inst Med Educ & Res PGIMER, Dept Pharmacol, Chandigarh 160012, India
[2] Panjab Univ, Univ Inst Pharmaceut Sci, Dept Pharmaceut, Chandigarh, Punjab, India
关键词
siRNA dose; Lipid nanoparticles; meta-analysis & systematic review; SMALL-INTERFERING RNA; ANTISENSE OLIGONUCLEOTIDES; LDL-CHOLESTEROL; DELIVERY; GENE; CLEARANCE; KNOCKDOWN; BIODISTRIBUTION; LIPOSOMES; DESIGN;
D O I
10.1016/j.ijbiomac.2024.133984
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 nano- formulations 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 nano- formulated 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.
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页数:14
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