Fluorometric measurement of creatine kinase activity.
نویسندگان
چکیده
SERUM CREATINE KINASE activity has beell measured by determining the amount of creatine liberated in the following reaction: ADI + creatine phosphate ATP + creatine. The Voges-Proskauer reactioii, production of a color by reaction of creatille with diacetyl alid -naphthol, has heeii used to measure enzymatically released creatine (1-5). The presence of a sulfhydryl compound in tile incubatioii mixture, necessary for the maintenance of a linear reaction rate, interferes with subsequent color development (2, 3, 6). This difficulty has been overcome by addition of the sulfhydryl reagent, p-chloromercuribenzoate, alid by prolonging the reaction time to 60 miii. (.2). in 1960, Conll reported a procedure for the determination of creatine, based upon the production of a fluophor with ninhydrin in strongly alkaline solution (7). His observations, that the method is less sensitive to sulfhydryl interference than is the Voges-Proskauer reaction, and that creatine phosphate is nonfluorogenic, suggested that the procedure might be readily adaptable to measurement of creatine kinase activity. This report describes such an application.
منابع مشابه
Observations on the fluorometric measurement of creatine kinase activity.
Twenty patients’ serums have been analyzed by both the Sax-Moore (1) and ConnAnido (2) creatine kinase methods. No significant difference in enzyme activity was found. In our hands, the Conn-Anido procedure, as originally described, gave variable results and high background fluorescence. The presence of high alkaline or acid phosphataseactivities in specimensanalyzed by the Sax-Moore procedure ...
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ورودعنوان ژورنال:
- Clinical chemistry
دوره 11 10 شماره
صفحات -
تاریخ انتشار 1965