Hemopyrrole and kryptopyrrole are absent from the urine of schizophrenics and normal persons.

1978 ◽  
Vol 24 (2) ◽  
pp. 230-233 ◽  
Author(s):  
P L Gendler ◽  
H A Duhan ◽  
H Rapoport

Abstract We describe a method for detecting hemopyrrole and kryptopyrrole in urine, with a detection limit of 100 mug/liter (1 part in 10(7)). Urine is thoroughly extracted with methylene chloride and the extract is concentrated and examined by gas chromatography and gas chromatography-mass spectrometry. No hemopyrrole or kryptopyrrole could be detected in 52 samples, from 17 controls, 29 schizophrenics, and six persons with acute intermittent porphyria.

1987 ◽  
Vol 65 (6) ◽  
pp. 1225-1227 ◽  
Author(s):  
B. K. Tang

A simple method using gas chromatography – mass spectrometry was developed to determine a low concentration of ethanol in urine. The detection limit was 0.02 mM ethanol. A mean ± SD ethanol concentration in urine of 0.21 ± 0.17 mM was measured in 11 alcoholics after 14 days abstention, a level at least 10 times higher than that of control subjects who had no alcoholic drinks during a period of 7 days prior to the test.


2004 ◽  
Vol 87 (5) ◽  
pp. 1098-1108 ◽  
Author(s):  
Olutosin R Idowu ◽  
Philip J Kijak ◽  
Jeffery R Meinertz ◽  
Larry J Schmidt

Abstract Chloramine-T is a disinfectant being developed as a treatment for bacterial gill disease in cultured fish. As part of the drug approval process, a method is required for the confirmation of chloramine-T residues in edible fish tissue. The marker residue that will be used to determine the depletion of chloramine-T residues from the edible tissue of treated fish is para-toluenesulfonamide (p-TSA), a metabolite of chloramine-T. The development and validation of a procedure for the confirmation of p-TSA is described. Homogenized fish tissue is dried by mixing with anhydrous sodium sulfate, and the mixture is extracted with methylene chloride. The extract is passed through a silica gel solid-phase extraction column, from which p-TSA is subsequently eluted with acetonitrile. The acetonitrile extract is evaporated, and the oily residue is dissolved in hexane. The hexane solution is shaken with fresh acetonitrile. The acetonitrile solution is evaporated and the residue is redissolved in dilute potassium hydroxide solution. The aqueous solution is extracted with methylene chloride to further remove more of the fat co-extractive. The aqueous solution is reacted with pentafluorobenzyl bromide in presence of tetrabutylammonium hydrogensulfate. The resulting di-(pentafluorobenzyl) derivative of p-TSA is analyzed by gas chromatography/mass spectrometry. This method permits the confirmation of p-TSA in edible fish tissue at 20 ppb.


2000 ◽  
Vol 83 (2) ◽  
pp. 290-298 ◽  
Author(s):  
Hing-Biu Lee ◽  
Thomas E Peart

Abstract Methods have been developed for the determination of bisphenol A (BPA) residues in municipal sewage and sludge samples. BPA in wastewater samples was enriched with a C18 solid-phase extraction cartridge, eluted with acetone, and converted to the pentafluoropropionyl derivative. For sludge samples, BPA was acetylated and extracted with supercritical carbon dioxide. In both cases, BPA-d16 was used as a surrogate to monitor extraction efficiency. Final analyses of derivatized sample extracts were performed by gas chromatography/mass spectrometry operating in the electron impact mode. For water samples, mean recoveries and standard deviations were 89 ± 6, 94 ± 4, and 85 ± 7% at fortification levels of 1, 0.1, and 0.025 μg/L, respectively, with a method detection limit of 0.006 μg/L. For solid waste samples, mean recoveries and standard deviations were 93 ± 5 and 92 ± 6% at fortification levels of 2.5 and 0.25 μg/g, respectively, and the method detection limit was 0.05 μg/g. For the Canadian samples under investigation, concentrations of BPA ranged from 49.9 to 0.031 μg/L in sewage influent and effluent, and from 36.7 to 0.104 μg/g in sludge.


Author(s):  
Susheela P ◽  
Rosaline Mary ◽  
Radha R

Objective: The objective of the present study was to determine the chemical compounds present in the nests of the mud dauber wasp, Sceliphron caementarium.Methods: Gas chromatography-mass spectrometry analysis of the nest samples was carried out by standard procedures. The resultant compounds were compared with the database of the National Institute Standard and Technology (NIST), WILEY8, FAME.Results: The results of the gas chromatography-mass spectrometry analysis of the concentrated ethanol extract revealed the presence of chemical compounds such as methylene chloride, 1, 1’:3’, 1’’-Terphenyl, 5’-Phenyl, Di N Decylsulfone, Eicosanoic acid, 1, 2-Bis (Trimethylsilyl) Benzene, and Androstane-11, 17-Dione, 3-[(Trimethylsilyl) Oxy]-, 17-[O-(Phenylmethyl) O.Conclusion: The compounds identified were found to have biological properties such as anti-inflammatory, antibacterial, and antifungal, and further study of these isolated compounds may prove their medicinal importance in future.


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