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采用差分pH技术测定脂肪酶活性。

Measurement of lipase activity by a differential pH technique.

作者信息

Ceriotti F, Bonini P A, Murone M, Barenghi L, Luzzana M, Mosca A, Ripamonti M, Rossi-Bernardi L

出版信息

Clin Chem. 1985 Feb;31(2):257-60.

PMID:3967357
Abstract

This is a new electrochemical method for determination of lipase activity in biological fluids, including serum, plasma, and duodenal juice. Advantages of turbidimetric methods--short reaction time, and small sample and reagent volumes--are combined with those of titrimetric methods: measurement of absolute activity (i.e., no standardization required), saturated substrate conditions, and direct measurement of reaction products. The proposed method is easy, inexpensive, and takes only 3 min. Precision is good: CV = 3.74% within day and 7.3% between days at the clinical-decision concentration, CV = 1.86% within day and 4.65% between days for above-normal lipase activities. The standard curve is linear up to 4500 U/L. Results (y) correlate well with those by turbidimetry (x): y = 0.9287x - 65.3 (r = 0.9719). Reference values are between 0 and 130 U/L.

摘要

这是一种用于测定生物体液(包括血清、血浆和十二指肠液)中脂肪酶活性的新型电化学方法。比浊法的优点——反应时间短、样品和试剂量小——与滴定法的优点相结合:绝对活性的测量(即无需标准化)、饱和底物条件以及反应产物的直接测量。所提出的方法简便、成本低,仅需3分钟。精密度良好:在临床决策浓度下,日内变异系数(CV)为3.74%,日间为7.3%;对于高于正常的脂肪酶活性,日内CV为1.86%,日间为4.65%。标准曲线在高达4500 U/L范围内呈线性。结果(y)与比浊法结果(x)相关性良好:y = 0.9287x - 65.3(r = 0.9719)。参考值在0至130 U/L之间。

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