Polyplexes and lipoplexes for mammalian gene delivery:: From traditional to microarray screening

被引:28
作者
How, SE
Yingyongnarongkul, B
Fara, MA
Diaz-Mochón, JJ
Mittoo, S
Bradley, M [1 ]
机构
[1] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
[2] Univ Ramkhamhaeng, Fac Sci, Dept Chem, Bangkok 10240, Thailand
关键词
transfection reagents; gene therapy; dendrimers; polyplexes; liposomes; cell-based microarrays; HTS;
D O I
10.2174/1386207043328616
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gene therapy requires the development of non-toxic and highly efficient delivery systems for DNA and RNAi Polycations, especially dendrimers, have shown enormous potential as gene transfer vehicles, displaying minimal toxicity with a broad range of cell lines. In this paper, a total of 13 dendrimers, up to G3.0, were constructed from AB(3) type isocyanate monomers using solid phase methodology and evaluated for transfection activity. Among the library of compounds prepared, a G3.0 dendrimer displayed comparable activity to Superfect. Gel retardation assays demonstrated that all of the compounds completely bound plasmid DNA, indicating the efficient formation of complexes between DNA and the dendrimers. A "transfection microarray" approach was developed for screening these compounds as well as a panel of lipoplexes (complexes of DNA with cationic lipids) and polyplexes (complexes of DNA with synthetic polycationic polymers), in 3D solution like micro-assay. Five cationic lipids with a cholesterol tail showed stronger or comparable transfection activity relative to Effectene. The new, micro-array screening method was rapid and miniaturized, offering the potential of high throughput screening of large libraries of transfection candidates, with thousands of library members per array, and the ability to rapidly screen a broad range of cell types.
引用
收藏
页码:423 / 430
页数:8
相关论文
共 39 条
[1]   Parallel synthesis and biophysical characterization of a degradable polymer library for gene delivery [J].
Akinc, A ;
Lynn, DM ;
Anderson, DG ;
Langer, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (18) :5316-5323
[2]   Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[3]   Semi-automated synthesis and screening of a large library of degradable cationic polymers for gene delivery [J].
Anderson, DG ;
Lynn, DM ;
Langer, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (27) :3153-3158
[4]  
[Anonymous], 1983, J IMMUNOL METH
[5]   DNA microarrays based on noncovalent oligonucleotide attachment and hybridization in two dimensions [J].
Belosludtsev, Y ;
Iverson, B ;
Lemeshko, S ;
Eggers, R ;
Wiese, R ;
Lee, S ;
Powdrill, T ;
Hogan, M .
ANALYTICAL BIOCHEMISTRY, 2001, 292 (02) :250-256
[6]   The interaction of plasmid DNA with polyamidoamine dendrimers: mechanism of complex formation and analysis of alterations induced in nuclease sensitivity and transcriptional activity of the complexed DNA [J].
Bielinska, AU ;
KukowskaLatallo, JF ;
Baker, JR .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1997, 1353 (02) :180-190
[7]   Molecular classification of cutaneous malignant melanoma by gene expression profiling [J].
Bittner, M ;
Meitzer, P ;
Chen, Y ;
Jiang, Y ;
Seftor, E ;
Hendrix, M ;
Radmacher, M ;
Simon, R ;
Yakhini, Z ;
Ben-Dor, A ;
Sampas, N ;
Dougherty, E ;
Wang, E ;
Marincola, F ;
Gooden, C ;
Lueders, J ;
Glatfelter, A ;
Pollock, P ;
Carpten, J ;
Gillanders, E ;
Leja, D ;
Dietrich, K ;
Beaudry, C ;
Berens, M ;
Alberts, D ;
Sondak, V ;
Hayward, N ;
Trent, J .
NATURE, 2000, 406 (6795) :536-540
[8]   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
[9]   Gene delivery with synthetic (non viral) carriers [J].
Brown, MD ;
Schätzlein, AG ;
Uchegbu, IF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 229 (1-2) :1-21
[10]   Preliminary characterization of novel amino acid based polymeric vesicles as gene and drug delivery agents [J].
Brown, MD ;
Schätzlein, A ;
Brownlie, A ;
Jack, V ;
Wang, W ;
Tetley, L ;
Gray, AI ;
Uchegbu, IF .
BIOCONJUGATE CHEMISTRY, 2000, 11 (06) :880-891