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Interference of non-specific peroxidases in the fluorescence detection of superoxide radical by hydroethidine oxidation: a new assay for H2O2

机译:非特异性过氧化物酶干扰氢乙啶氧化法检测超氧自由基的荧光:H2O2的新测定

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摘要

The present study shows that hydroethidine (HE), used for in-vivo qualitative fluorescent detection of superoxide anion, can be also oxidized by H2O2 via non-specific peroxidase (horseradish peroxidase and myeloperoxidase) catalysis, forming fluorescent oxidation products. These products give broad excitation/emission peaks (490-495/580-600 nm) near the excitation/emission peaks (475/580 nm) of the HE-superoxide oxidation product, and this may pose serious interference problems to the fluorescent detection of the superoxide radical. The study suggests cautionary use of the HE-superoxide anion assay mainly for detection of reactive oxygen species. A byproduct of this study was the development of a simple and sensitive HE-horseradish peroxidase assay for the in-vitro quantification of H2O2 in biological tissues with a sensitivity of 1 mu mol L-1 stop.
机译:本研究表明,用于体内定性荧光超氧化物阴离子检测的氢乙啶(HE)也可以通过非特异性过氧化物酶(辣根过氧化物酶和髓过氧化物酶)催化被H2O2氧化,形成荧光氧化产物。这些产物在HE超氧化物氧化产物的激发/发射峰(475/580 nm)附近给出宽的激发/发射峰(490-495 / 580-600 nm),这可能对荧光检测产生严重的干扰问题。超氧自由基。研究表明,谨慎使用HE超氧化物阴离子测定法主要用于检测活性氧。这项研究的副产品是开发一种简单而灵敏的HE辣根过氧化物酶测定法,用于体外定量生物组织中的H2O2,其灵敏度为1μmol L-1终止。

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