Hepatocyte-Specific Gene Delivery with Galactose-Bearing Cationic Polymers with Different Molecular Structures

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Since the promising virus -based gene therapies are often limited by problems such as the immunity of virus itself, the development of an efficient non-viral vector is of prime importance. For this reason, several synthetic nonviral polymeric carriers including cationic sequences have been molecularly designed. It is well known that the polymeric carriers with some cationic groups buffer the endosomal pH resulting in the enhanced transfection efficiency, but also in a relatively high toxicity. In the last decades, the polymers bearing pendant carbohydrates (glycopolymers) was proved to have relatively less toxic. Since the glycopolymers may not only decrease the toxicity of the cationic chain but also serve as targeting agent, we have rationally designed new glycopolymer-based gene delivery carriers. The interaction of carrier/gene polyplexes with hepatocytes and their intracellular trafficking were investigated in vitro. Our results show the significant efficacy of the galactose moieties on the uptake by hepatocytes, in a ligand specific manner.

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86-91

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September 2012

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© 2013 Trans Tech Publications Ltd. All Rights Reserved

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[1] J. C. Cohen, A. Pertsemlidis, I. K Kotowski, R. Graham, C. K. Garcia and H. H. Hobbs, Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9, Nat Genet 37(2005) 161–165.

DOI: 10.1038/ng1509

Google Scholar

[2] J.C. Cohen, E. Boerwinkle, T.H. Mosley,and H.H. Hobbs, Sequence variations in PCSK9, low LDL, and protection against coronary heart disease. N Engl J Med 354(2006) 1264–1272.

DOI: 10.1056/nejmoa054013

Google Scholar

[3] P.van de Wetering, N.M.E. Schuurmans-Nieuwenbroek, W. E. Hennink, and G. Storm, Comparative transfection studies of human ovarian carcinoma cells in vitro, ex vivo and in vivo with poly(2-(dimethylamino)ethyl methacrylate)-based polyplexes. The Journal of Gene Medicine 1 (199)156–165.

DOI: 10.1002/(sici)1521-2254(199905/06)1:3<156::aid-jgm29>3.0.co;2-o

Google Scholar

[4] J.S. Wang, K. Matyjaszewski, Controlled Living Radical Polymerization – Halogen Atom-Transfer Radical Polymerization Promoted by a Cu(I)Cu(II) Redox Process. Macromolecules 28,( 1995) 7901-7910.

DOI: 10.1021/ma00127a042

Google Scholar

[5] J.S. Wang, K. Matyjaszewski, Controlled/"Living" Radical Polymerization. Atorm Transfer Radical Polymerization in the Presence of Transition-Metal Complex. J Am. Chern. Soc. 117(1995) 5614-5615.

DOI: 10.1021/ja00125a035

Google Scholar

[6] V. Percec, B. Barboiu, A. Neumann, J.C. Ronda, M. Zhao, Metal-catalyzed "Living" Radical Polymerization of Styrene Initiated with Arenesulfonyl Chlorides. From Heterogeneous to Homogeneous Catalysis. Macromolecules 29(1996) 3665-3668.

DOI: 10.1021/ma960061a

Google Scholar

[7] T. Grimaud, K. Matyjaszewski, Controlled "Living" Radical Polymerization of Methyl Methacrylate by Atom Transfer Radical Polymerization. Macromolecules 30(1997) 2216-2216.

DOI: 10.1021/ma961796i

Google Scholar

[8] B. Bramlage, S. Alefelder , J.L. Marschall ,F. Eckstein , Nucleic acid res, 27(1999) 3159.

Google Scholar