CREATININE ASSAY BY A REACTION-KINETIC PRINCIPLE
CREATININE ASSAY BY A REACTION-KINETIC PRINCIPLE
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DOI:
10.1016/0009-8981(72)90513-x
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发表时间:
1972-01-01
影响因子:
5
通讯作者:
LARSEN, K
中科院分区:
文献类型:
--
作者:
LARSEN, K
A reaction-kinetic assay of serum and urine creatinine with the Jaffé reaction but without deproteinization is described. All reaction parameters have been investigated to find optimal conditions for the application of the reaction-kinetic principle. The reaction course shows greater pH dependence during the first minute than during the following minutes and the buffer capacity of serum protein reduces the reaction rate relative to that in a serum-free reaction mixture; correction for this can be made by using a suitable constant factor for serum. Beyond the buffer effect protein does not influence the reaction rate; thus deproteinization is unnecessary. Serum may contain Jaffé-positive compounds reacting faster than creatinine—acetoacetate is an example—and also contain compounds reacting slower than creatinine. Measurements during the second minute give values comparable to non-kinetic methods with Lloyd's reagent. Values from measurements during the first minute are on an average about 17 μmole/1 higher than second minute values, but 14 μmole/l lower than by a non-kinetic method without Lloyd's reagent. The reaction-kinetic principle carried out with the LKB 8600 Reaction Rate Analyzer is very simple and has proved extremely reliable. The time required per sample is 1 2–2 min depending on demands for precision and especially for specificity. Reference (normal) ranges found by measurements during the first minute: males 80–138 μmole/l, females 63–121 μmole/l and during the second minute: males 69–117 μmole/l, females 53–101 μmole/l.