Abstract
A sensitive and specific high performance liquid chromatographic method for the simultaneous determination of cyanate and carbamyl phosphate was established. The chromatographic conditions were as follows: column, TSK gel SAX (4 mm I.D.X50 mm); eluent, 0.075 M NaCI; column temperature, 20°C. The detection was based on the indophenol reaction of ammonia which was released by the hydrolysis of cyanate or carbamyl phosphate. To suppress their hydrolysis during the sample preparation, the deproteinization of biological samples with trichloroacetic acid was carried out at 0°C, and the interval between addition of trichloroacetic acid and neutralization was restricted to 20 s. Taking advantages of the sensitivity and precision of the present method, we developed a procedure that permits measurement of concentrations of cyanate as low as 0.8 μM and those of carbamyl phosphate as low as 0.5 μM in samples of whole blood and liver extract. © 1986, The Japan Society for Analytical Chemistry. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Koshiishi, I., Isono, J., & Imanari, T. (1986). Simultaneous Determination of Cyanate and Carbamyl Phosphate by High Performance Liquid Chromatography. Analytical Sciences, 2(1), 81–85. https://doi.org/10.2116/analsci.2.81
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.