Kularatne Ruvanthi N, Crist Rachael M, Stern Stephan T
Nanotechnology Characterization Laboratory, Cancer Research Technology Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research Sponsored by the National Cancer Institute, Frederick, MD 21702, USA.
Pharmaceuticals (Basel). 2022 Jul 20;15(7):897. doi: 10.3390/ph15070897.
The earliest example of in vivo expression of exogenous mRNA is by direct intramuscular injection in mice without the aid of a delivery vehicle. The current state of the art for therapeutic nucleic acid delivery is lipid nanoparticles (LNP), which are composed of cholesterol, a helper lipid, a PEGylated lipid and an ionizable amine-containing lipid. The liver is the primary organ of LNP accumulation following intravenous administration and is also observed to varying degrees following intramuscular and subcutaneous routes. Delivery of nucleic acid to hepatocytes by LNP has therapeutic potential, but there are many disease indications that would benefit from non-hepatic LNP tissue and cell population targeting, such as cancer, and neurological, cardiovascular and infectious diseases. This review will concentrate on the current efforts to develop the next generation of tissue-targeted LNP constructs for therapeutic nucleic acids.
外源性mRNA体内表达的最早例子是在不借助递送载体的情况下直接对小鼠进行肌肉注射。治疗性核酸递送的当前技术水平是脂质纳米颗粒(LNP),它由胆固醇、辅助脂质、聚乙二醇化脂质和含可电离胺的脂质组成。肝脏是静脉给药后LNP积累的主要器官,肌肉注射和皮下给药后也会有不同程度的观察到LNP积累。通过LNP将核酸递送至肝细胞具有治疗潜力,但许多疾病适应症将受益于非肝脏LNP组织和细胞群体靶向,如癌症、神经、心血管和传染病。本综述将集中于目前为开发用于治疗性核酸的下一代组织靶向LNP构建体所做的努力。