A study of the reaction of urea with diacetyl monoxime and diacetyl.

نویسندگان

  • R Lugosi
  • R J Thibert
  • W J Holland
  • L K Lam
چکیده

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منابع مشابه

Determination of Urea in Blood and Urine with Diacetyl Monoxime-glucuronolactone Reagent.

N UMEROUS STUDIES have been reported in the literature on the photometric determination of urea in biological fluids with diacetyl monoxime as the color-developing agent. The reaction is photosensitive, does not follow Beer’s law, and requires special precautions for reproducible results. In many proposed procedures, oxidants were added in the reaction mixture to destroy hydroxylamine which mig...

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Improvements in the determination of urea using diacetyl monoxime; methods with and without deproteinisation.

A rapid and reproducible method is described for measurement of urea in biological materials (after deproteinisation) and in serum (without deproteinisation). Urea is colorimetrically determined with diacetyl monoxime and thiosemicarbazide in the presence of sulphuric acid, phosphoric acid and ferric chloride. The sensitivity of the colorimetric reaction and stability of the colour are enhanced...

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A new colorimetric method for the determination of urea nitrogen in blood with diacetyl monoxime-glucuronolactone-glucosaccharodilactone reagent.

In a previous paper,3) a colorimetric method for the determination of urea nitrogen in blood and urine was presented on the basis of a color reaction of urea with diacetyl monoxime (DAM) in phosphoric acid solution in the presence of D-glucuronolactone (GL), which served to produce a photo-stable color and eliminate the sigmoidal nature of calibration curve observed usually in the DAM method.4)...

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The automated thiosemicarbazide-diacetyl monoxime method for plasma urea.

IN RECENT YEARS the automated diacetyl monoxime (DAM) reaction as adapted to the AutoAnalyzer has become the method of choice in many clinical laboratories for the determination of urea in biologic fluids. The method is based on the condensation of urea with diacetyl, the latter usually being liberated from the monoxime in the presence of one of various acid reagents (1, 2). The reaction, howev...

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Chemical inhibition used in a kinetic urease/glutamate dehydrogenase method for urea in serum.

We describe a fixed-time-interval, kinetic inhibition method, with use of a competitive inhibitor (l) of the urease/glutamate dehydrogenase reaction to increase the "apparent" Michaelis constant by a factor of (1 + [l]lKl). This allows greater flexibility in selecting an appropriate sample dilution for kinetic determinations of urea in serum (i.e., [S]lKm ratio). Nine compounds were screened as...

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عنوان ژورنال:
  • Clinical biochemistry

دوره 5 3  شماره 

صفحات  -

تاریخ انتشار 1972