首页> 外文期刊>Analytica chimica acta >Superoxide generated by pyrogallol reduces highly water-soluble tetrazolium salt to produce a soluble formazan: A simple assay for measuring superoxide anion radical scavenging activities of biological and abiological samples
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Superoxide generated by pyrogallol reduces highly water-soluble tetrazolium salt to produce a soluble formazan: A simple assay for measuring superoxide anion radical scavenging activities of biological and abiological samples

机译:邻苯三酚产生的超氧化物还原高度水溶性的四唑盐以产生可溶性甲maz:一种用于测定生物和非生物样品超氧化物阴离子自由基清除活性的简单测定法

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摘要

Superoxide anion radical (O2~-) plays an important role in several human diseases. The xanthine/xanthine oxidase system is frequently utilized to produce (V. However, false positive results are easily got by using this system. The common spectrophotometric probes for O2~- are nitroblue tetrazolium (NBT) and cytochrome c. Nevertheless, the application of NBT method is limited because of the water-insolubility of NBT formazan and the assay using cytochrome c lacks sensitivity and is not suitable for microplate measurement. We overcome these problems by using 1,2,3-trihydroxybenzene (pyrogallol) as O2~-generating system and a highly water-soluble tetrazolium salt, 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disu!fophenyl)-2H-tetrazolium sodium salt (WST-1) which can be reduced by superoxide anion radical to a stable water-soluble formazan with a high absorbance at 450 nm. The method is simple, rapid and sensitive. Moreover, it can be adapted to microplate format. In this study, the O2~- scavenging activities of superoxide dismutase (SOD), L-ascorbic acid, N-acetyl-L-cysteine (NAC), albumin from human serum, flavonoids and herbal extracts were assessed by using this method. Meanwhile, the activities of tissue homogenates and serum were determined by using this validated method. This method, applicable to tissue homogenates, serum and herbal extracts, proved to be efficient for measuring O2~- scavenging activities of biological and abiological samples.
机译:超氧阴离子自由基(O2〜-)在几种人类疾病中起重要作用。黄嘌呤/黄嘌呤氧化酶系统经常被用来生产(V。但是,使用该系统很容易产生假阳性结果。O2〜-的分光光度探针通常是硝基蓝四唑(NBT)和细胞色素c。由于NBT甲maz的水不溶性,NBT方法受到局限,并且使用细胞色素c的测定法灵敏度低且不适合微板测量,我们通过使用1,2,3-三羟基苯(邻苯三酚)生成O2〜来解决这些问题。体系和高度水溶性的四唑盐,2-(4-碘苯基)-3-(4-硝基苯基)-5-(2,4-二氟苯基)-2H-四唑钠盐(WST-1)可以通过超氧阴离子自由基将其还原为稳定的水溶性甲for,在450 nm处具有较高的吸收率,该方法简便,快速,灵敏,并且适用于微孔板形式,本研究中的O2〜-清除活性超氧化物歧化酶(SOD),L-抗坏血酸,N-乙酰基-L-半胱氨酸用这种方法评估了人参碱(NAC),人血清中的白蛋白,类黄酮和草药提取物。同时,通过该验证方法确定组织匀浆和血清的活性。该方法适用于组织匀浆,血清和草药提取物,被证明可有效地测量生物和非生物样品的O2〜-清除活性。

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