Mutagenicity of 30 chemicals and human urine specimens in S. typhimurium strains with various nitroreductase or acetyltransferase activities

Author(s):  
P. Einistö ◽  
T. Nohmi ◽  
M. Watanabe ◽  
M. Ishidate
Keyword(s):  
1976 ◽  
Vol 68 (2) ◽  
pp. 273-281 ◽  
Author(s):  
C. L. COPE ◽  
S. LOIZOU

SUMMARY The nature of the urinary conjugate converted by solvolysis, to free unconjugated deoxycorticosterone (DOC) was studied. A comparison of 11 solvolysis techniques has shown that the method employed in this study yielded 86% of the highest yield by any of the techniques tried. Three successive chromatographic systems on paper showed that no appreciable amounts of contaminants were present in the free DOC eluates, following solvolysis. By preparing authentic [3H]DOC sulphate and subjecting it to solvolysis it was shown that more than 90% of the tritiated DOC was recovered, after chromatography of the free DOC extract. This suggests that much of the solvolysable DOC in human urine is present in the form of the sulphate conjugate. The levels of DOC, excreted as the solvolysable conjugate in a variety of urine specimens, were shown to be much higher than those of free DOC, the former being 4·8 to 127 times higher than the amount of the latter. This highly variable ratio suggests that the site of production of solvolysable DOC is different from that for free DOC. The only correlation between free and solvolysable DOC was shown in dexamethasone-suppressed patients, in whom the mean percentage remaining after suppression was 30·6% for free DOC, 24·1% for solvolysable DOC and 22·2% for cortisol. As solvolysable DOC is present in much larger amounts in urine, care is necessary in the storage of urine samples in which free DOC estimates are to be made, as we found that urine specimens left at room temperature for 1 week could show rises of as much as 400% of their starting free DOC levels.


2019 ◽  
Vol 11 (9) ◽  
pp. 1377-1386 ◽  
Author(s):  
Belal Haschimi ◽  
Lukas Mogler ◽  
Sebastian Halter ◽  
Arianna Giorgetti ◽  
Bernd Schwarze ◽  
...  

1971 ◽  
Vol 17 (9) ◽  
pp. 875-881 ◽  
Author(s):  
Norman Weissman ◽  
Mei Lee Lowe ◽  
John M Beattie ◽  
James A Demetriou

Abstract A simple, convenient method is described for the detection in human urine of three major classes of drugs of abuse: amphetamines, barbiturates, and alkaloids. The drugs are adsorbed from urine by a column of non-ionic resin (Amberlite XAD-2), eluted with methanol, and chromatographed on a thin-layer silica gel plate. The drugs are made visible and identified by a series of procedures involving exposure to ultraviolet radiation, heat treatment, sequential spraying with group-specific reagents, and measurement of Rf values. Detection limits for 5-ml urine specimens are: 0.4 µg per ml for amphetamines and barbiturates, and 0.8 g per ml for alkaloids. The test requires 6 h to perform. One technologist can process 50 specimens per day.


1964 ◽  
Vol 206 (5) ◽  
pp. 1106-1110 ◽  
Author(s):  
Max J. Seijffers ◽  
Harry L. Segal ◽  
Leon L. Miller

Human urine has been fractionated on diethylaminoethyl cellulose to yield two pepsinogens. They have been called pepsinogen II and pepsinogen III on the basis of chromatographic behavior identical to that of fundic mucosal pepsinogens II and III. Pepsinogen I has been found absent from 23 urine specimens of 12 individuals. Results suggest a gross qualitative and quantitative correlation between pepsinogen II-pepsinogen III ratio (in terms of total proteolytic activity) in urine and gastric mucosa.


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