Lactosylated chitosan for DNA delivery into hepatocytes: The effect of lactosylation on the physicochemical properties and intracellular trafficking of pDNA/chitosan complexes
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作者:
Hashimoto, M
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机构:Keio Univ, Fac Sci & Technol, Yokohama, Kanagawa 2238522, Japan
Hashimoto, M
Morimoto, M
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机构:Keio Univ, Fac Sci & Technol, Yokohama, Kanagawa 2238522, Japan
Morimoto, M
Saimoto, H
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机构:Keio Univ, Fac Sci & Technol, Yokohama, Kanagawa 2238522, Japan
Saimoto, H
Shigemasa, Y
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机构:Keio Univ, Fac Sci & Technol, Yokohama, Kanagawa 2238522, Japan
Shigemasa, Y
Sato, T
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机构:Keio Univ, Fac Sci & Technol, Yokohama, Kanagawa 2238522, Japan
Sato, T
机构:
[1] Keio Univ, Fac Sci & Technol, Yokohama, Kanagawa 2238522, Japan
[2] Tottori Univ, Fac Engn, Tottori 6808552, Japan
Chitosan is a useful nonviral vector for gene delivery. To make a pDNA/chitosan complex specific to hepatocytes, lactose-modified chitosan (lac-chitosan) was synthesized. When the percentage of lactose residues substituted was 8%, lac-chitosan showed excellent DNA-binding ability, good protection of DNA from nuclease, and the suppression of self-aggregation and serum-induced aggregation. Although the cellular uptake efficiency of the pDNA/lac-chitosan complex was almost the same as that of the pDNA/chitosan complex, the cell transfection efficiency of the former was greater for HepG2 cells having asialoglycoprotein receptors. Inhibitor of endocytosis such as bafilomycin A(1) and nocodazole significantly reduced the transfection efficiency of the pDNA/lac-chitosan complex. Observations with a confocal laser scanning microscope indicated that the pDNA/lac-chitosan complexes traversed endocytic compartments more rapidly than the pDNA/chitosan complex. Furthermore, the pDNA/lac-chitosan complexes were delivered to the late endosome and have the advantage of delivering DNA to the perinuclear region.