Artigo Revisado por pares

Star-Shaped Poly(ethylene glycol)- b lock -polyethylenimine Copolymers Enhance DNA Condensation of Low Molecular Weight Polyethylenimines

2002; American Chemical Society; Volume: 3; Issue: 5 Linguagem: Inglês

10.1021/bm025539z

ISSN

1526-4602

Autores

Holger Petersen, Klaus Kunath, Alison Martin, Snow Stolnik, Clive J. Roberts, Martyn C. Davies, Thomas Kissel,

Tópico(s)

DNA and Nucleic Acid Chemistry

Resumo

Star-shaped poly(ethylene glycol)-block-polyethylenimine [star-(PEG-b-PEI)] significantly enhance plasmid DNA condensation of low molecular weight (MW) PEIs. The star-block copolymers were prepared via a facile synthesis route using hexamethylene diisocyanate as linker between PEG and PEI blocks. NMR and FT-IR spectroscopy confirmed the structures of intermediately activated PEG and final products. Furthermore, the copolymers were characterized by size exclusion chromatography, static light scattering, and viscosimetry. Their molecular weights (Mw 19−26 kDa) were similar to high MW PEI (25 kDa). Thermoanalytical investigations (thermogravimetric analysis, differential scanning calorimetry) were also performed and verified successful copolymer synthesis. DNA condensation with the low MW PEIs (800 and 2000 Da) and their 4- and 8-star-block copolymers was studied using atomic force microscopy, dynamic light scattering, zeta-potential measurements, and ethidium bromide (EtBr) exclusion assay. It was found that low MW PEIs formed huge aggregates (500 nm to 2 μm) in which DNA is only loosely condensed. By contrast, the star-block copolymers yielded small (80−110 nm), spherical and compact complexes that were stable against aggregation even at high ionic strength and charge neutrality. Furthermore, as revealed in the EtBr exclusion assay these star-block copolymers exhibited a DNA condensation potential as high as high MW PEI. Since these star-(PEG-block-PEI) copolymers are composed of relatively nontoxic low MW PEI and biocompatible PEG, their potential as gene delivery agents merits further investigations.

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