番红褪色法检测羟自由基清除效果研究

祁红兵, 陆萍, 陈钧

祁红兵, 陆萍, 陈钧. 番红褪色法检测羟自由基清除效果研究[J]. 信阳师范学院学报(自然科学版), 2009, 22(3): 448-450.
引用本文: 祁红兵, 陆萍, 陈钧. 番红褪色法检测羟自由基清除效果研究[J]. 信阳师范学院学报(自然科学版), 2009, 22(3): 448-450.
QI Hong-bing, LU Ping, CHEN Jun. The Method of Detecting Hydroxyl Radical Scavenged by Faded Safranine[J]. Journal of Xinyang Normal University (Natural Science Edition), 2009, 22(3): 448-450.
Citation: QI Hong-bing, LU Ping, CHEN Jun. The Method of Detecting Hydroxyl Radical Scavenged by Faded Safranine[J]. Journal of Xinyang Normal University (Natural Science Edition), 2009, 22(3): 448-450.

番红褪色法检测羟自由基清除效果研究

基金项目: 

信阳师院青年骨干教师资助计划

The Method of Detecting Hydroxyl Radical Scavenged by Faded Safranine

  • 摘要: 根据Fenton反应原理,利用番红作为显色剂检测由EDTANa2-Fe(Ⅱ)-H2O2体系产生的.OH.番红褪色光度法测定清除羟自由基的最佳反应条件为:往10 mL具塞试管中,依次加入pH7.4的磷酸缓冲液1.0mL,番红溶液(520 mg/L)0.2 mL,EDTANa2-Fe(Ⅱ)(0.003 8 mol/L)1.0 mL,不同浓度的样品溶液0.1mL,最后加入0.25%H2O20.5 mL,双蒸水稀释至刻度后于40℃保温30 min,紫外-可见分光光度法519 nm处测吸光度A.
    Abstract: Based on the priciple of Fenton reaction,the ·OH produced by the EDTANa2-Fe(Ⅱ)-H2O2 system can be detected by using safranine as developer.The optimal experimental conditions is evaluated: 1.0 mL pH7.4 phosphate buffer;safranine(520 mg/L) 0.2 mL,EDTANa2-Fe(Ⅱ)(0.003 8 mol/L) 1.0 mL,and 0.25% H2O2 0.5 mL.All these agent must be added one by one into the 10 mL capped test tube.Redistilled water was diluted to graduation line,then incubated at 40 ℃.The amount of hydroxyl radical produced in the system can be in...
  • [1] 张立伟,王金山,江崇球. 超临界流体CO_2萃取中药有效成分的抗氧化性的分光光度法研究[J]. 光谱学与光谱分析, 2004,(09) .
    [2] 张丽平,童华荣. 抗氧化能力测定方法的研究进展[J]. 中国食品添加剂, 2004,(03)
    [3] 曹国锋,翁新楚. 鱼油氧化稳定性的研究(Ⅱ)[J]. 中国油脂, 1995,(05) .
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出版历程
  • 收稿日期:  2008-11-10
  • 发布日期:  2009-07-09

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