Human serum albumin-polyethylenimine nanoparticles for gene delivery

被引:154
作者
Rhaese, S
von Briesen, H
Rübsamen-Waigmann, H
Kreuter, J
Langer, K
机构
[1] Univ Frankfurt, Bioctr, Inst Pharmaceut Technol, D-60439 Frankfurt, Germany
[2] Chemotherapeut Forschungsinst Georg Speyer Haus, D-60596 Frankfurt, Germany
[3] Bayer AG, Geschaftsbereich Pharma, D-42096 Wuppertal, Germany
关键词
nanoparticles; gene delivery; human serum albumin;
D O I
10.1016/S0168-3659(03)00302-X
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoparticles consisting of DNA, human serum albumin (HSA) and polyethylenimine (PEI) were formed and tested for transfection efficiency in vitro with the aim of generating a nonviral gene delivery vehicle. HSA-PEI-DNA nanoparticles containing the pGL3 vector coding for luciferase as reporter gene were formed by charge neutralization. The particles were characterized by gel retardation assay, dynamic light scattering (size) and electrophoretic mobility measurements (charge). Stability was determined by spectrophotometric analysis and transfection efficiency was evaluated in cell culture using human embryonic epithelial kidney 293 cells. HSA-PEI-DNA nanoparticles were prepared by co-encapsulation of PEI as a lysosomotropic agent at varying nitrogen to phosphate (N/P) ratios. An optimum transfection efficiency was achieved when the particles were prepared at N/P ratios between 4.8 and 8.4. Furthermore, they displayed a low cytotoxicity when tested in cell culture. Our results show that HSA-PEI-DNA nanoparticles are a versatile carrier for DNA that may be suitable for i.v. administration. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:199 / 208
页数:10
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