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Synthesis of Poly(vinyl alcohol)/C60 and Poly(N‐vinylpyrrolidone)/C60 Nanohybrids as Potential Photodynamic Cancer Therapy Agents
Authors:Marie Hurtgen  Antoine Debuigne Dr  Ange Mouithys‐Mickalad  Robert Jérôme Prof  Christine Jérôme Prof  Christophe Detrembleur Dr
Institution:1. Center for Education and Research on Macromolecules (CERM), University of Liège, Sart‐Tilman, B6a, 4000 Liège (Belgium), Fax: (+32)?4‐366‐34‐97;2. Center for Oxygen Research and Development (CORD), University of Liège, Sart‐Tilman, B6a, 4000 Liège (Belgium)
Abstract:Well‐defined poly(vinyl acetate) (PVAc) and poly(N‐vinylpyrrolidone)‐co‐poly(vinyl acetate) (PNVP‐co‐PVAc) chains end‐capped by Co(acac)2 (acac=acetylacetonate) and prepared by cobalt‐mediated radical polymerization (CMRP) are grafted onto a fullerene. Homolytic Co? C bond cleavage of the polymer chain ends at 30 °C releases the polymeric radicals that add onto C60, thereby leading to the corresponding PVAc/C60 and PNVP‐co‐PVAc/C60 nanohybrids. The polymer–Co(acac)2]/C60] molar ratio was varied to adjust the structure of the nanohybrids, and more particularly the number of grafted arms. Finally, the potential of the hydrosoluble PVOH/C60 nanohybrids, which result from the methanolysis of the ester groups of PVAc/C60, and of the PNVP‐co‐PVAc/C60 nanohybrids as photosensitizers for photodynamic therapy (PDT), was approached. First, photobleaching tests demonstrated the ability of these nanohybrids to produce singlet oxygen upon irradiation, which can play a role in cell damage. Second, cell viability assays demonstrated that both types of nanohybrids are deprived of intrinsic cytotoxicity in the dark, whereas they promoted significant cell mortality when subjected to light treatment. The selective response of these materials to irradiation makes them promising compounds for PDT.
Keywords:cobalt  fullerenes  nanostructures  photosensitizers  polymerization
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