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Synthesis,antitumour and DNA replication activities of polymers containing vinyl‐(5‐fluorouracil)‐ethanoate
Authors:Nam‐In Kang  Sun‐Mi Lee  Mizuo Maeda  Chang‐Sik Ha  Won‐Jei Cho
Abstract:A new monomer, vinyl‐(5‐fluorouracil)‐ethanoate (VFUE), was synthesized by reaction of 5‐fluorouracil (5‐FU) and vinyl iodoacetate. The homopolymer of VFUE and its copolymers with acrylic acid (A, A) and maleic anhydride (MAH) were prepared by photopolymerization. The synthesized VFUE and polymers were identified by FTIR, 1H NMR and 13C NMR spectroscopies. The contents of VFUE unit in poly(VFUE‐co‐AA) and poly(VFUE‐co‐MAH) were 21 mol% and 16 mol%, respectively. The number average molecular weights of the polymers determined by gel permeation chromatography were in the range 9600–17900 g mol?1. The in vitro cytotoxicities of the samples against a normal cell line decreased as follows: 5‐FU > VFUE > poly(VFUE) > poly(VFUE‐co‐AA) > poly(VFUE‐co‐MAH). The in vivo antitumour activities of the polymers against Balb/C mice bearing the sarcoma 180 tumour cells were greater than those of 5‐FU at all concentrations. The inhibition of simian virus 40 DNA replication by the samples was much greater than that of the control. © 2002 Society of Chemical Industry
Keywords:polymer prodrug  vinyl‐(5‐fluorouracil)‐ethanoate  polymers containing VFUE  in vitro antitumour activity  in vivo antitumour activity  DNA replication
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