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测量血清脂肪酶活性的荧光法。

Fluorometric method for measuring serum lipase activity.

作者信息

Rietz B, Guilbault G C

出版信息

Clin Chem. 1975 Nov;21(12):1788-90.

PMID:810273
Abstract

We describe a method for determining lipase (triacylglycerol acyl-hydrolase, EC 3.1.1.3) activity in serum. Emulsified olive oil in tris(hydroxymethyl)aminomethane buffer is used as substrate. The course of the enzymatic reaction is followed by measuring the decrease in fluorescence with time of a fluorescent indicator, 4-methylumbelliferone, added to the substrate, caused by the change in the pH of the substrate solution resulting from the reaction. All measurements are performed at 37 degrees C. The reaction volume is about 2.3 ml, in a Pyrex cuvette. Change of fluorescence and of enzyme activity are linearly related in the range of 77.8 to 389.0 U/liter. An assay can be done in as little as 3 to 5 min, with excellent precision.

摘要

我们描述了一种测定血清中脂肪酶(三酰甘油酰基水解酶,EC 3.1.1.3)活性的方法。以三(羟甲基)氨基甲烷缓冲液中的乳化橄榄油作为底物。通过测量添加到底物中的荧光指示剂4-甲基伞形酮的荧光随时间的降低来跟踪酶促反应过程,这种降低是由反应导致的底物溶液pH变化引起的。所有测量均在37℃下进行。反应体积约为2.3 ml,在派热克斯玻璃比色皿中进行。在77.8至389.0 U/升的范围内,荧光变化与酶活性呈线性关系。一次测定最短可在3至5分钟内完成,精密度极佳。

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