• DocumentCode
    3107029
  • Title

    Biological Oxidation Resistance of L-Ascorbic Acid Cellulose Ester

  • Author

    Liu Ning ; Fang Gui-zhen ; Chen Shujuan ; Lu Zhan-guo ; Su Shuang ; Liu Tao ; Su Rongjun

  • Author_Institution
    Inst. of Food & Eng., Harbin Univ. of Commerce, Harbin, China
  • fYear
    2010
  • fDate
    18-20 June 2010
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    L-ascorbic acid and sodium carboxymethylcellulose were taken as raw material to synthesize polymer material L-ascorbic acid cellulose ester which had antioxidation effect. Antioxidation effect of o benzylgalloyl microcrystalline cellulose ester was appraised in vitro. The results showed that all the different concentrations L-ascorbic acid cellulose ester significantly improved GSH-Px activity of mice liver. But there was no significant difference among the low dose, middle dose and high dose group. Consequently, it can not explain that there was dose-effect relationship between them. L-ascorbic acid cellulose ester could significantly inhibit generation of lipid peroxidation product malondialdehyde(MDA) and oxidative hemolysis of erythrocyte, and there was very significantly dose-response relationship between them. It can provide technical foundation for the further study on anti-oxidative new functional polymer materials.
  • Keywords
    biochemistry; biological tissues; biomedical materials; blood; cellular biophysics; liver; molecular biophysics; organic compounds; oxidation; polymers; L-ascorbic acid cellulose ester; antioxidation effect; antioxidative new functional polymer materials; benzylgalloyl microcrystalline cellulose ester; biological oxidation resistance; dose-effect relationship; dose-response relationship; erythrocyte; inhibit generation; lipid peroxidation; malondialdehyde; mice liver; oxidative hemolysis; polymer material; red blood cell; sodium carboxymethylcellulose; Appraisal; Biological materials; Immune system; In vitro; Lipidomics; Liver; Mice; Oxidation; Polymers; Raw materials;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
  • Conference_Location
    Chengdu
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-4712-1
  • Electronic_ISBN
    2151-7614
  • Type

    conf

  • DOI
    10.1109/ICBBE.2010.5515788
  • Filename
    5515788