Modified polyethylenimines as non viral gene delivery systems for aerosol therapy:: effects of nebulization on cellular uptake and transfection efficiency

被引:36
作者
Dailey, LA
Kleemann, E
Merdan, T
Petersen, H
Schmehl, T
Gessler, T
Hänze, J
Seeger, W
Kissel, T
机构
[1] Univ Marburg, Dept Pharmaceut & Biopharm, D-35032 Marburg, Germany
[2] Univ Giessen, Dept Internal Med, D-35392 Giessen, Germany
关键词
aerosol; PEI; non-viral; nebulization; lung;
D O I
10.1016/j.jconrel.2004.08.031
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study examined the effect of nebulization on the cellular uptake and transfection efficiency of polyplexes from four polyethylenimine (PEI) modifications: branched 25 kDa PEI (bPEI), linear 22 kDa PEI (linPEI), pegylated PEI (pegPEI) and biodegradable PEI (bioPEI). Polyplexes were aerosolized with air-jet and ultrasonic nebulizers. The aerosol was collected and used to determine complex size and zeta potential. Fluorescence-assisted cell sorting (FACS) was used to quantify the cellular association of polyplexes in primary alveolar cells (AEC), A549 cells and primary bronchial cells (BEC). Confocal laser scanning microscopic images provided information about the internalization of polyplexes. Transfection efficiencies of polyplexes were quantified via measurement of luciferase expression. All polymers were stable during nebulization, although size increases were observed after air-jet nebulization. FACS studies showed a two- to three-fold increase in polyplex association with BEC compared to A549 cells, while polyplex association with AEC was negligible. BPEI, linPEI and bioPEI polyplexes were internalized, while pegPEI polyplexes remained predominately attached to the cellular membrane. Luciferase expression was detected only in BEC and A549 cells with transfection efficiencies approximately one order of magnitude higher in BEC. All PEI modifications investigated were suitable for aerosol therapy, although cell type and polymer structure significantly influenced the uptake and transfection efficiency of the polyplexes. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:425 / 436
页数:12
相关论文
共 42 条
[1]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[2]  
Bragonzi A., 2002, Current Gene Therapy, V2, P295, DOI 10.2174/1566523023347832
[3]   Aerosol delivery of robust polyethyleneimine-DNA complexes for gene therapy and genetic immunization [J].
Densmore, CL ;
Orson, FM ;
Xu, B ;
Kinsey, BM ;
Waldrep, JC ;
Hua, P ;
Bhogal, B ;
Knight, V .
MOLECULAR THERAPY, 2000, 1 (02) :180-188
[4]   Efficient gene delivery into human dendritic cells by adenovirus polyethylenimine and mannose polyethylenimine transfection [J].
Diebold, SS ;
Lehrmann, H ;
Kursa, M ;
Wagner, E ;
Cotten, M ;
Zenke, M .
HUMAN GENE THERAPY, 1999, 10 (05) :775-786
[5]  
Erbacher P, 1999, J GENE MED, V1, P210
[6]   ExGen 500 is an efficient vector for gene delivery to lung epithelial cells in vitro and in vivo [J].
Ferrari, S ;
Moro, E ;
Pettenazzo, A ;
Behr, JP ;
Zacchello, F ;
Scarpa, M .
GENE THERAPY, 1997, 4 (10) :1100-1106
[7]   Barriers to and new approaches for gene therapy and gene delivery in cystic fibrosis [J].
Ferrari, S ;
Geddes, DM ;
Alton, EWFW .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (11) :1373-1393
[8]   A novel non-viral vector for DNA delivery based on low molecular weight, branched polyethylenimine:: Effect of molecular weight on transfection efficiency and cytotoxicity [J].
Fischer, D ;
Bieber, T ;
Li, YX ;
Elsässer, HP ;
Kissel, T .
PHARMACEUTICAL RESEARCH, 1999, 16 (08) :1273-1279
[9]   Microparticulate uptake mechanisms of in-vitro cell culture models of the respiratory epithelium [J].
Foster, KA ;
Yazdanian, M ;
Audus, KL .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (01) :57-66
[10]   Enhanced gene expression in mouse lung after PEI-DNA aerosol delivery [J].
Gautam, A ;
Densmore, CL ;
Xu, B ;
Waldrep, JC .
MOLECULAR THERAPY, 2000, 2 (01) :63-70