Swami Archana, Kurupati Raj K, Pathak Atul, Singh Y, Kumar P, Gupta K C
Institute of Genomics and Integrative Biology, Mall Road, Delhi University Campus, Delhi 110 007, India.
Biochem Biophys Res Commun. 2007 Nov 3;362(4):835-41. doi: 10.1016/j.bbrc.2007.08.073. Epub 2007 Aug 27.
Delivery of DNA and siRNA into mammalian cells is a powerful technique in treating various diseases caused by single gene defects. Herein, we report a highly efficient delivery system using 1,4-butanediol diglycidyl ether (bisepoxide) crosslinked polyethylenimine (PEI) nanoparticles (PN). The nanoparticle/DNA complexes (nanoplexes) exibited approximately 2.5- to 5.0-fold gene transfer efficacy and decreased cytotoxicity in cultured cell lines, compared to the native PEI (25 kDa) (gold standard) and commercially available transfection agents such as Lipofectamine 2000 and Fugene. The bisepoxide crosslinking results in change in amine ratio in PEI; however, it retains the net charge on PN unaltered. A series of nanoparticles obtained by varying the degree of crosslinking was found to be in the size range of 69-77 nm and the zeta potential varying from +35 to 40 mV. The proposed system was also found to deliver siRNA efficiently into HEK cells, resulting in approximately 70% suppression of the targetted gene (GFP).
将DNA和小干扰RNA(siRNA)导入哺乳动物细胞是治疗由单基因缺陷引起的各种疾病的一项强大技术。在此,我们报道了一种使用1,4 - 丁二醇二缩水甘油醚(双环氧化合物)交联聚乙烯亚胺(PEI)纳米颗粒(PN)的高效递送系统。与天然PEI(25 kDa)(金标准)以及市售转染试剂如Lipofectamine 2000和Fugene相比,纳米颗粒/DNA复合物(纳米复合物)在培养细胞系中表现出约2.5至5.0倍的基因转移效率,并降低了细胞毒性。双环氧化合物交联导致PEI中胺比例发生变化;然而,它使PN上的净电荷保持不变。通过改变交联程度获得的一系列纳米颗粒的尺寸范围为69 - 77 nm,ζ电位在 +35至40 mV之间变化。还发现所提出的系统能够有效地将siRNA递送至人胚肾细胞(HEK细胞),导致靶向基因(绿色荧光蛋白,GFP)的表达受到约70%的抑制。