A Receptor-mediated Gene Delivery System Using Streptavidin and Biotin-derivatized, Pegylated Epidermal Growth Factor

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An efficient receptor-mediated non-viral gene delivery formulation based on mono-pegylated recombinant human epidermal growth factor (EGF) was developed using a streptavidin-biotin system. Biotin-derivatized and mono-pegylated EGF was prepared by conjugating a biotin-PEG-NHS derivative to EGF and purified through a chromatographic method. Luciferase plasmid DNA and polyethylenimine (PEI) were complexed to form positively charged nanoparticles on which negatively charged streptavidin was first coated and then biotin-PEG-EGF conjugate was immobilized via streptavidin-biotin interaction. The EGF-PEG-biotin-streptavidin-PEI-DNA complexes were characterized in terms of their effective diameter and surface zeta (zeta)-potential value under various formulation conditions. The formulated complexes exhibited high transfection efficiency (similar to10(8) in luciferase activity) with no inter-particle aggregation. This was attributed to enhanced cellular uptake of the resultant complexes via receptor-mediated endocytosis. Furthermore, in the presence of serum proteins, a slight decrease in transfection efficiency was observed due to the presence of PEG chains on the surface. (C) 2002 Elsevier Science B.V. All rights reserved.
Publisher
Elsevier Science Bv
Issue Date
2002-09
Language
English
Article Type
Article
Keywords

BLOCK-COPOLYMER; T-LYMPHOCYTES; CELLS; DNA; TRANSFECTION; EXPRESSION; BINDING; PEPTIDE; RESISTANCE; INHIBITION

Citation

JOURNAL OF CONTROLLED RELEASE, v.83, no.1, pp.109 - 119

ISSN
0168-3659
URI
http://hdl.handle.net/10203/11045
Appears in Collection
BS-Journal Papers(저널논문)
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