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
Link To Document :
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