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Determination of Hydrogen Peroxide by Iron(III) Complex of Thiacalix[4]arenetetrasulfonate on a Modified Ion-Exchanger with Peroxidase-like Catalytic Activity

机译:改性过的具有类似过氧化物酶活性的离子交换剂上的硫杂杯[4]芳烃四磺酸铁(III)配合物测定过氧化氢

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摘要

An iron(III) complex of thiacalix[4]arenetetrasulfonate on a modified anion-exchanger (Fe3+-TCASA-500) has shown high peroxidase-like activity at pH 5 - 6 for the reaction of quinoid-dye formation between 3-methyl-2-benzothiazolinone hydrazone and N-(3-sulfopropyl)aniline in the presence of hydrogen peroxide. Utilizing the peroxidase-like activity of Fe3+-TCASA-500 for this reaction, a method using Fe3+-TCASA-500 was applied for the spectrophotometric determination of hydrogen peroxide. The calibration curve by the method using Fe3+-TCASA-500 was linear over the range from 1 to 10 μg of hydrogen peroxide in a 1 ml sample solution. The apparent molar absorptivity for hydrogen peroxide was 2.4 × 104 l mol-1 cm-1, which was about 80% of that by peroxidase under the same conditions. This determination method of hydrogen peroxide using Fe3+-TCASA-500 was applied for the determination of glucose in diluted normal and abnormal control serum I and II.
机译:在修饰的阴离子交换剂(Fe3 + -TCASA-500)上的噻唑烷[4]亚芳基四磺酸盐的铁(III)络合物在pH 5-6下显示出高过氧化物酶样活性,可用于3-甲基-在过氧化氢存在下的2-苯并噻唑啉酮和N-(3-磺丙基)苯胺。利用Fe3 + -TCASA-500的过氧化物酶样活性进行反应,使用Fe3 + -TCASA-500的方法用于分光光度法测定过氧化氢。在1 ml样品溶液中,使用Fe3 + -TCASA-500的方法的校准曲线在1至10μg过氧化氢的范围内呈线性。过氧化氢的表观摩尔吸收率为2.4×104 l mol-1 cm-1,约为相同条件下过氧化物酶的表观摩尔吸收率的80%。使用Fe3 + -TCASA-500的过氧化氢测定方法用于测定稀释的正常和异常对照血清I和II中的葡萄糖。

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