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[Polyfection as nonviral gene transfer method -design of novel nonviral vector using alpha-cyclodextrin].

Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan (2004-07-06)
Hidetoshi Arima
RESUMEN

Due to the growing concerns over the toxicity and immunogenicity of viral DNA delivery systems, DNA delivery via nonviral routes has become more desirable and advantageous. In particular, polycation complexes with DNA (polyplex) are attractive nonviral vectors. To design novel polycationic vectors, we prepared polyamidoamine starburst dendrimer (dendrimer) conjugates with three cyclodextrins (CDE conjugates) and three generations (G2, G3, and G4) of dendrimers. Of seven CDE conjugates, an alpha-CDE conjugate (G3) with an average degree of substitution (DS) of alpha-CyD of 2.4 [alpha-CDE conjugate (G3, DS 2.4)] showed greater gene transfer activity than dendrimers and other alpha-CDE conjugates with less cytotoxicity. These results suggest the potential use of alpha-CDE conjugate (G3, DS 2.4) as a polycationic vector in vitro and in vivo. Herein, I review a recent polyfection method, with special focus on alpha-CDE conjugate (G3, DS 2.4).

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Sigma-Aldrich
α-Cyclodextrin, ≥98%
Sigma-Aldrich
α-Cyclodextrin, Produced by Wacker Chemie AG, Burghausen, Germany, Life Science, 98.0-101.0% cyclodextrin basis (HPLC)
Sigma-Aldrich
α-Cyclodextrin, produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (HPLC)
Sigma-Aldrich
α-Cyclodextrin, powder, BioReagent, suitable for cell culture, ≥98%
Sigma-Aldrich
α-Cyclodextrin, purum, ≥98.0% (HPLC)
USP
Alpha Cyclodextrin, United States Pharmacopeia (USP) Reference Standard
Alfadex, European Pharmacopoeia (EP) Reference Standard