CONDUCTIVITY METHOD FOR DETERMINATION OF UREA
CONDUCTIVITY METHOD FOR DETERMINATION OF UREA
复制标题
DOI:
10.1021/ac60180a039
复制
发表时间:
1961-01-01
影响因子:
7.4
通讯作者:
KROONTJE, W
中科院分区:
文献类型:
--
作者:
CHIN, WT;KROONTJE, W
Standard solutions were prepared containing C “-acetylated isoniazidalone and in combination with C “isoniazid and isonicotinic acid, these three substances comprising the major fraction of isoniazid and metabolites found in human urine and plasma (6). The radioisotopically labeled compounds were diluted with carrier, so that the specific activity was approximately equal for each metabolite. Urine samples con-taining 100 Mg. per ml. of each C “-labeled metabolite and plasma samples containing 10 and 1.0 Mg· per ml. were analyzed for acetylated isoniazid. The results are shown in Table I. C “-labeled isoniazid was administered to both human volunteers and male Sprague Dawley rats. Urine samples collected from these subjects were analyzed for acetylated isoniazid. The column effluent thus obtained was lyophilized, redissolved in a small amount of distilled water, and subjected to chromatographic analysis on What-man No. 1 filter paper strips with de-velopment by butyl alcohol-water (1 to 1) or isopropyl alcohol-water (85 to 15). Urine samples before column analysis and solutions containing isoniazid, isonicotinic acid, and acetylated isoniazid were run simultaneously with the column effluent. Autoradiograms were made of these strips, which were subsequently developed colorimetrically.