Klose S, Stoltz M, Munz E, Portenhauser R
Clin Chem. 1978 Feb;24(2):250-5.
This report describes a new specific colorimetric procedure for uric acid assay with AutoAnalyzer II and SMA (Technicon) systems, made specific by the application of uricase. Hydrogen preroxide, formed in this reaction, effects the oxidative coupling of 4-aminophenazone and 2,4-dichlorophenol under the catalytic influence of peroxidase. The red dye formed is measured at 505 or 520 nm. A sample blank measurement is not necessary, and the reagents show very good stability. The test shows linearity up to 714 mumol of uric acid per liter. Results of thie method correlate very well with those by the uricase-ultraviolet and uricase--catalase methods. There is no interference by hemoglobin, bilirubin, lipemia, and various drugs, except a minor interference by alpha-methyldopa. Interference from ascorbate is eliminated by ascorbate oxidase. This method can be regarded as a considerably improved routine test for uric acid on continuous-flow systems in clinical laboratories as compared with the commonly used phosphotungstate method.
本报告介绍了一种使用自动分析仪II和SMA(Technicon)系统进行尿酸测定的新型比色法,该方法通过应用尿酸酶而具有特异性。此反应中生成的过氧化氢在过氧化物酶的催化作用下,促使4-氨基苯乙酮和2,4-二氯苯酚发生氧化偶联。生成的红色染料在505或520nm处进行测定。无需进行样品空白测量,且试剂具有很好的稳定性。该检测方法在每升714微摩尔尿酸范围内呈线性。此方法的结果与尿酸酶-紫外法和尿酸酶-过氧化氢酶法的结果相关性非常好。除α-甲基多巴有轻微干扰外,血红蛋白、胆红素、脂血和各种药物均无干扰。抗坏血酸氧化酶可消除抗坏血酸的干扰。与常用的磷钨酸盐法相比,该方法可被视为临床实验室连续流动系统上尿酸常规检测的显著改进。