Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), Av. Barcelona s/n, Campus Vida, University de Santiago de Compostela, 15782 Santiago de Compostela, Spain; Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain; IDIS Research Institute, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain.
Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), Av. Barcelona s/n, Campus Vida, University de Santiago de Compostela, 15782 Santiago de Compostela, Spain; IDIS Research Institute, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain.
J Control Release. 2024 Aug;372:295-303. doi: 10.1016/j.jconrel.2024.06.051. Epub 2024 Jun 24.
Lipid nanoparticles (LNPs) currently dominate the RNA delivery landscape; however their limited diffusivity hampers targeted tissue dissemination, and, hence, their capacity for intracellular drug delivery. This is especially relevant for tissues such as the central nervous system (CNS), where overcoming proactive brain barriers is crucial for the efficacy of genetic therapeutics. This research aimed to create ionizable nanoemulsions (iNEs), a new generation of RNA delivery systems with enhanced diffusivity. The developed iNEs (consisting of the combination of C12-200, DOPE, Vitamin E, and DMG-PEG) with a size below 100 nm, neutral surface charge, and high RNA loading capacity, showed excellent cell viability and transfection efficiency in various cellular models, including neurons, astrocytes, and microglia. Subsequently, iNEs containing mRNA GFP were tested for CNS transfection, highlighting their exceptional diffusivity and selective transfection of neurons following intra-parenchymal administration.
脂质纳米颗粒(LNPs)目前主导着 RNA 递药领域;然而,其有限的扩散性阻碍了靶向组织的扩散,从而限制了其细胞内药物递药的能力。这在中枢神经系统(CNS)等组织中尤为重要,因为克服主动脑屏障对于基因治疗的疗效至关重要。本研究旨在开发离子型纳米乳液(iNEs),这是一种具有增强扩散性的新一代 RNA 递药系统。所开发的 iNEs(由 C12-200、DOPE、维生素 E 和 DMG-PEG 组合而成)的粒径小于 100nm,表面电荷呈中性,并且具有高 RNA 负载能力,在包括神经元、星形胶质细胞和小胶质细胞在内的各种细胞模型中显示出优异的细胞活力和转染效率。随后,对含有 GFP mRNA 的 iNEs 进行了 CNS 转染测试,突出显示了其在脑实质内给药后异常的扩散性和对神经元的选择性转染。