Multilayers based on cationic nanocomplexes for co-delivery of doxorubicin and DNA

•Nanocomplex is prepared by using polyethyleneimine-ferrocene, doxorubicin and DNA.•Multilayers are fabricated through layer-by-layer assembly of the nanocomplexes.•Doxorubicin release is triggered by oxidation of ferrocene.•Cells are transfected by the multilayers through the substrate-mediated mod...

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Published inColloids and surfaces, B, Biointerfaces Vol. 112; pp. 67 - 73
Main Authors Sun, Jie-kan, Ren, Ke-feng, Zhu, Lei-ze, Ji, Jian
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.12.2013
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Summary:•Nanocomplex is prepared by using polyethyleneimine-ferrocene, doxorubicin and DNA.•Multilayers are fabricated through layer-by-layer assembly of the nanocomplexes.•Doxorubicin release is triggered by oxidation of ferrocene.•Cells are transfected by the multilayers through the substrate-mediated mode. Co-delivery of drugs and genes has synergistic advantages in many fields such as cancer treatments. In this study, we present a multilayers for co-delivery of doxorubicin (DOX) and DNA. Ferrocene-modified polyethyleneimine (PEI-Fc) is synthesized, and it can form micelles in solution with ferrocene core and PEI shell. DOX and DNA are thus incorporated into the core and shell of the micelles, respectively, to form the PEI-Fc–DOX–DNA nanocomplexes. Such cationic nanocomplexes are used to construct multilayers through layer-by-layer assembly with negatively charged dextran sulfate (DS). We show that the multilayers can release DOX, and the release can be significantly enhanced in a hydrogen peroxide condition. Moreover, the multilayers have the ability to transfect cells through a substrate-mediated mode. The (PEI-Fc–DOX–DNA/DS) multilayers can be potentially applied to the biomedical devices for cancer treatment, regenerative medicine, etc.
Bibliography:http://dx.doi.org/10.1016/j.colsurfb.2013.07.044
ObjectType-Article-1
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ISSN:0927-7765
1873-4367
DOI:10.1016/j.colsurfb.2013.07.044