期刊文献+

低分子量磺化壳聚糖的制备及其抗氧化活性研究 被引量:2

Preparation of low molecular-weight sulfated chitosan and its antioxidative activity
原文传递
导出
摘要 均相体系中,采用H2O2氧化降解法得到低分子量壳聚糖;以其为原料,氯磺酸—二甲基甲酰胺(DMF)为磺化试剂,在较温和的条件下制备低分子量磺化壳聚糖(S-LCTS),产物分子量较磺化壳聚糖(S-CTS)显著降低。红外光谱分析表明,所得产物在1236cm-1和808cm-1处有特征吸收,分别显示出-SO3H基团中S=O和C-O-S的伸缩振动。本文还检测了所得产物对超氧自由基(O2-·)、过氧化氢(H2O2)以及1,1-二苯代苦味酰基自由基(DPPH·)的清除效果。实验结果显示,S-LCTS对O2-·、H2O2和DPPH·的清除效果明显优于S-CTS,显示了良好的抗氧化活性。 Low molecular-weight chitosan was prepared first by oxidative degradation with hydroperoxide(H2O2) under homogeneous conditions. And then, with it as raw material, chlorosulfonic acid (HClSO3)in N, N-dimethylformamide(DMF) as sulfated agent, low molecular-weight sulfated chitosan(S-LCTS) was obtained under mild conditions, and its molecular-weight was considerably lower than normal suffated chitosan (S-CTS). FTIR spectrum showed that the product had characteristic absorptions at 1236cm^-1 and 808cm^-1, due to sulfo groups, assigned to S = O and C- O- S bond stretchings, respectively. Moreover, the scavenging effects of the product on superoxide radical( O2^-·), hydrogen peroxide ( H2O2 ), and 1,1- diphenyl-2- picrylhydrazyl( DPPH · ) was determined.The results indicated that the scavenging effects of S-LCTS were much superior to S-CTS' and it showed favorable antioxidative activity.
出处 《食品工业科技》 CAS CSCD 北大核心 2008年第12期97-100,共4页 Science and Technology of Food Industry
关键词 低分子量磺化壳聚糖 抗氧化活性 超氧自由基 过氧化氢 DPPH· low molecular-weight chitosan antioxidative activity superoxide radical hydrogen peroxide DPPH ·
  • 相关文献

参考文献3

二级参考文献26

共引文献128

同被引文献13

  • 1姜雪松,王勃生,沈琮,李晓光,孙福玉.甲壳素及其衍生物的生物活性和医学应用[J].生物医学工程学杂志,1996,13(4):353-356. 被引量:28
  • 2沈江波 林建立 张世馥.壳聚糖对人子宫颈癌HeLa细胞生长作用的研究.解剖学报,1997,28(4):421-421.
  • 3Ormrrod D J, Holmes C C, Miller T E. Dietary chitiosan in hibits hypercholesterolaemia and atherogenesis in the apoli poprotein Ddefrcient mouse model of atherosclerosis [J]. Atherosclerosis, 1998, 138(2): 329 -334.
  • 4Hirano S, Tanaka Y, Hasegawa M, et al. Effect of sulfated derivatives of chitosan on some blood coagulant factors[J].CarbohydrRes, 1985, 137:205.
  • 5Guminska M, Ignacak J, Wojcik E. In vitro inhibitory effect of chitosan and it's a degradation products on energy metah olism in Ehrlieh ascites turnout cells[J]. Pol J Pharmacol, 1996, 48(5): 495-501.
  • 6Ikuo S, Jun M, Motowo N, et al. Inhibition by Sulfated Chitin Derivati ves of Invasion through Extracellular Ma- trix and Enzymatic Degradation by Metastatic Melannoma Ceils [J]. CancerRes, 1990, 50(12) : 3631-3637.
  • 7Anzai N, Taniyama T, Nakandakari N. et al. Inhibition of DNA adduct formation and mutagenic action of 3 amino-- 1 methyl 5 hpyrido[4,3-b] indole by chlorophyllin chitosan in rpsI. transgenc mice [J]. Jpn J Cancer Res, 2001, 92 (8): 848-853.
  • 8Hasegawa M, Yagi K, lwakawa S, et al. Chitosan induces apoptosis viacaspase 3 activation in bladder tumor cells[J]. Jpn J Cancer Res, 2001, 92(4): 459-466.
  • 9周南进,曹俊,丁斌,谢勇,陈江,刘东升.壳聚糖及其衍生物对肝癌细胞SMMC7721的生长抑制作用[J].中国生化药物杂志,2007,28(5):312-314. 被引量:6
  • 10蒋珍菊,王周玉,胡星琪.壳聚糖类肝素衍生物抗凝血性能研究[J].化学与生物工程,2008,25(12):57-59. 被引量:10

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部