Chaix Arnaud, Cueto-Diaz Eduardo, Delalande Anthony, Knezevic Nikola, Midoux Patrick, Durand Jean-Olivier, Pichon Chantal, Cunin Frederique
Institut Charles Gerhardt Montpellier, Charles Gerhardt Montpellier, Université de Montpellier UMR 5253 CNRS-ENSCM-UM2-UM1, 2 Place Eugène Bataillon 34095 Montpellier Cedex 05 France
Centre de Biophysique Moléculaire in Orleans (CBM) UPR4301 France.
RSC Adv. 2019 Oct 7;9(55):31895-31899. doi: 10.1039/c9ra05461h.
Porous silicon nanoparticles as a novel platform in gene therapy, have shown to be an efficient vehicle for the delivery of nucleic acids in cells. For the first time, a family of porous silicon nanoparticles has been produced featuring an amino-acid functionalized cationic external surface aiming at pDNA complexation. The amino acid-based pDNA nanocarriers, displaying an average diameter of 295 nm, succeeded in transfection of HEK293 cells with an efficiency 300 times superior to "bare" porous silicon nanoparticles.
多孔硅纳米颗粒作为基因治疗中的一种新型平台,已被证明是细胞中核酸递送的有效载体。首次制备了一类多孔硅纳米颗粒,其具有氨基酸功能化的阳离子外表面,旨在实现与质粒DNA(pDNA)的复合。基于氨基酸的pDNA纳米载体平均直径为295纳米,成功转染了人胚肾293(HEK293)细胞,其效率比“裸”多孔硅纳米颗粒高出300倍。