Ionizable nanoemulsions for RNA delivery into the central nervous system - importance of diffusivity

被引:3
|
作者
Borrajo, Mireya L. [1 ,2 ,3 ]
Quijano, Aloia [1 ,3 ]
Lapuhs, Philipp [1 ,2 ,3 ]
Rodriguez-Perez, Ana I. [1 ,3 ,4 ]
Anthiya, Shubaash [1 ,2 ,3 ]
Labandeira-Garcia, Jose L. [1 ,3 ,4 ]
Valenzuela, Rita [1 ,3 ,4 ]
Alonso, Maria Jose [1 ,2 ,3 ]
机构
[1] Univ Santiago de Compostela, Ctr Res Mol Med & Chron Dis CiMUS, Ave Barcelona S-N,Campus Vida, Santiago De Compostela 15782, Spain
[2] Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15782, Spain
[3] Univ Santiago de Compostela, IDIS Res Inst, Santiago De Compostela 15782, Spain
[4] Networking Res Ctr Neurodegenerat Dis CIBERNED, Madrid, Spain
基金
欧盟地平线“2020”;
关键词
Brain delivery; Diffusivity; mRNA; Nanoemulsion; RNA therapeutics; siRNA; RATIONAL DESIGN; DRUG-DELIVERY; NANOPARTICLES; NANOCAPSULES; ENDOCYTOSIS; MECHANISMS; ACID;
D O I
10.1016/j.jconrel.2024.06.051
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 intraparenchymal administration.
引用
收藏
页码:295 / 303
页数:9
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