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Poly(ethylene imine)‐ g ‐chitosan using EX‐810 as a spacer for nonviral gene delivery vectors
Author(s) -
Lou YuLun,
Peng YuShiang,
Chen BingHung,
Wang LiFang,
Leong Kam W.
Publication year - 2008
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.31961
Subject(s) - gene delivery , ethylene glycol , chitosan , transfection , cytotoxicity , materials science , green fluorescent protein , polyelectrolyte , imine , fluorescence microscope , polymer chemistry , lipofectamine , nuclear chemistry , polymer , biophysics , chemistry , organic chemistry , biochemistry , fluorescence , in vitro , biology , recombinant dna , gene , vector (molecular biology) , physics , quantum mechanics , catalysis
Polyelectrolyte complexes have been widely studied as gene carriers in recent years. In this study, poly (ethylene imine) was grafted onto chitosan (PEI‐ g ‐CHI) as a nonviral gene carrier in order to improve the water solubility as well as the inherent transfection efficiency of chitosan. We present a novel method to conjugate the amine or hydroxyl groups of chitosan (CHI) and the amine groups of PEI through opening the epoxide rings of ethylene glycol diglycidyl ether (EX‐810), which also brings the merits as mentioned in PEGylation chemistry. The degree of substitution of PEI onto CHI was characterized by NMR. The preliminarily cellular mechanisms, from the cellular entry to the endosomal release, were investigated by the correlations among the physicochemical properties of the DNA‐polymer complexes, the buffering capacity of the modified polymer, the cytotoxicity, and the efficiency of the transgene expression. The cytotoxicity assayed by MTT shows that cell viability of PEI‐ g ‐CHI is higher than CHI especially noticeable at high concentrations using human kidney 293T cells. The efficiency of transgene expression and the amount of intracellular plasmid were monitored using green fluorescent protein (GFP) and visualized by fluorescence microscopy. The transfection efficiency of PEI‐ g ‐CHI/DNA polyplex is significantly better than CHI/DNA polyplex when using the weight ratios higher than 2.5. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009

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