A new gene delivery formulation of polyethylenimine/DNA complexes coated with PEG conjugated fusogenic peptide

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A fusogenic peptide, KALA, was conjugated with poly(ethylene glycol) (PEG) for use as an endosome disruptive agent in the gene delivery formulation of polyethyleneimine (PEI). A maleimide terminated methoxy-PEG, a cysteine specific derivative, was reacted with KALA to produce a PEG-KALA conjugate. The conjugate was analyzed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry, and its hemolytic activity was determined relative to KALA. Positively charged PEG-KALA conjugate was coated onto the surface of negatively charged DNA/PEI complexes to form net positively charged PEG-KALA/DNA/PEI complexes. They were 200-400 nm in diameter with increasing amount of PEG-KALA, whereas DNA/PEI complexes coated with KALA aggregated to a great extent. This was because PEG chains surrounding the surface of the complexes suppressed the inter-particle interaction that was mediated by cationic KALA. Transfection efficiency progressively increased as the amount of PEG-KALA to be coated was increased, suggesting that fusogenic activity of KALA contributes to enhancing the level of gene expression. (C) 2001 Elsevier Science B.V. All rights reserved.
Publisher
Elsevier Science Bv
Issue Date
2001-09
Language
English
Article Type
Article
Keywords

MEDIATED ENDOCYTOSIS PATHWAY; DNA DELIVERY; TRANSFECTION EFFICIENCY; IN-VITRO; CELLS; RECEPTOR; SYSTEMS; VECTOR; HEPATOCYTES; GROWTH

Citation

JOURNAL OF CONTROLLED RELEASE, v.76, no.1-2, pp.183 - 192

ISSN
0168-3659
URI
http://hdl.handle.net/10203/11844
Appears in Collection
BS-Journal Papers(저널논문)
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