Linxiang Li, Abe Yoshihiro, Nagasawa Yukiko, Kudo Risa, Usui Noriko, Imai Kazuhiro, Mashino Tadahiko, Mochizuki Masataka, Miyata Naoki
Kyoritsu College of Pharmacy, 1-5-30 Shibakoen, Minato, Tokyo 105-8512, Japan.
Biomed Chromatogr. 2004 Sep;18(7):470-4. doi: 10.1002/bmc.339.
An HPLC assay for hydroxyl radicals is described. The hydroxyl radical was trapped by terephthalic acid (non-fluorescent), and 2-hydroxyl terephthalic acid (fluorescent) was quantitated by HPLC-fluorescence detection. At a terephthalic acid concentration of 4.25 mmol/L, the hydroxyl radical formed in the Fenton reaction was successfully assayed in the concentration range of hydrogen peroxide of 2.5-50 micro mol/L, where the concentration of Fe(II) was 50 micro mol/L. The fluorescence of 2-hydroxy terephthalate was stable at 24 h, and its detection limit by this method was 5 nmol/L (100 fmol).
本文描述了一种用于检测羟基自由基的高效液相色谱(HPLC)分析方法。羟基自由基由对苯二甲酸(无荧光)捕获,通过HPLC-荧光检测对2-羟基对苯二甲酸(有荧光)进行定量分析。在对苯二甲酸浓度为4.25 mmol/L时,成功测定了在Fenton反应中生成的羟基自由基,其中过氧化氢浓度范围为2.5 - 50微摩尔/升,亚铁离子(Fe(II))浓度为50微摩尔/升。2-羟基对苯二甲酸酯的荧光在24小时内保持稳定,该方法对其检测限为5纳摩尔/升(100飞摩尔)。