EXCRETION OF BILE ACIDS BY THREE MEN ON A FAT-FREE DIET

1966 ◽  
Vol 44 (6) ◽  
pp. 957-969 ◽  
Author(s):  
S. S. Ali ◽  
A. Kuksis ◽  
J. M. R. Beveridge

A combination of thin-layer chromatography and gas–liquid chromatography was used for the separation and determination of fecal bile acids in three middle-aged men during the last 4 days of three 8-day periods on a fat-free diet. The range of the total output was 130–650 mg/day. Lithocholic and deoxycholic acids were the major components and accounted for 65–80% of the total excretion of bile acids. Other common bile acids were present in considerably smaller quantities (0.5–11% each). In addition, evidence was obtained for the presence of a number of as yet unreported fecal bile acids. These were tentatively identified as 3α,12β-dihydroxy-, 3β,12β-dihydroxy-, 3α,7β-dihydroxy-, 3α-monohydroxy-7-keto-, 12α-monohydroxy-3-keto-, and 7β-monohydroxy-cholanic and cholanic acids. The latter three acids occurred in traces only, but the other uncommon fecal bile acids each accounted for 0.5–7% of the total excretion of bile acids. Significant variations were found in the concentrations of several of the bile acids both between different samples from the same subject and between samples from different subjects.

Author(s):  
A.A. Parshutina ◽  
◽  
A.A. Solovyova ◽  
L.P. Satyukova ◽  
E.G. Shubina ◽  
...  

The article shows the importance of the study of feed for broiler chickens on the content of organochlorine pesticides. These substances in significant concentrations can disrupt the development of birds and cause mass poisoning. The study of formula feed for broiler chickens «prestart» and «start» by two methodswas conducted: a certified method for the determination of organochlorine pesticides in feed and formula feed (thin layer chromatography) and a method for detecting pesticides not certified for feed (gas-liquid chromatography with mass spectrometer detector). During the experiment, the presence of organochlorine pesticides in several formulafeed samples was revealed.


1967 ◽  
Vol 50 (3) ◽  
pp. 615-623
Author(s):  
Kenneth T Hartman

Abstract Gas-liquid chromatography (GLC) following conventional isolation procedures has been used to clean up pesticide residues for confirmation by thin layer chromatography (TLC). This procedure is more rapid and efficient than present cleanup procedures and permits the determination of pesticide residues that do not survive these rigorous acid or alkali treatments. The method also permits TLC confirmation of pesticide residues that have similar Rf values but different GLC retention times. Recoveries ranged from 85 to 105% for 25 of 28 pesticides tested


Author(s):  
S. Barnes ◽  
A. Chitranukroh

A simple and reproducible method using the non-ionic resin, Amberlite XAD-7, for the isolation of bile acids from serum by a batch procedure is described. Recoveries were greater than 95% for the non-sulphated bile acids and greater than 70% for the sulphate esters of bile acids. By using 1 g of resin, recoveries were independent of the mass (0.1–5 μmol) of the bile acid present. Up to 35 samples a day can be extracted without requiring dedication of the operator. When serum extracts were analysed by the 3α-hydroxysteroid dehydrogenase procedure for estimation of bile acids, virtually all the background fluorescence was eliminated. These extracts were also suitable for gas liquid chromatography, thin layer chromatography, and radioimmunoassay.


1995 ◽  
Vol 78 (1) ◽  
pp. 115-117 ◽  
Author(s):  
Carmen Rossini ◽  
Enrique Pandolfi ◽  
Eduardo Dellacassa ◽  
Patrick Moyna

Abstract A thin-layer chromatography (TLC) method with scanning is described for evaluation of the 1,8-cineole content of Eucalyptus essential oils. Samples were developed on silica gel G 60 with light petroleum–chloroform (70 + 30) as mobile phase. Color was developed with 4-dimethylaminobenzal-dehyde–sulfuric acid reagent. The absorbance of colored spots was measured at 460 nm. The response was linear between 15 to 75 μg of 1,8-cineole, with a correlation coefficient of 0.9997. The results of each assay were compared with those from gas–liquid chromatography (GLC). The TLC to GLC ratio was constant (0.92).


1975 ◽  
Vol 147 (3) ◽  
pp. 435-438 ◽  
Author(s):  
M Rangarajan ◽  
A Darbre

A method is described for the identification of amino acid thiohydantoins by two-dimensional t.l.c. An indirect method for the determination of amino acid thiohydantoins is described which, after hydrolysis, the corresponding amino acids are determined by g.l.c.


1977 ◽  
Vol 23 (9) ◽  
pp. 1640-1643 ◽  
Author(s):  
G Nicolau ◽  
G Van Lear ◽  
B Kaul ◽  
B Davidow

Abstract We describe a micromethod for determining as little as 0.1 microgram of morphine per liter of human urine. The procedure is about 20-fold more sensitive than are currently used gas-liquid chromatographic methods. It is particularly suitable for use as a confirmatory method for large-scale radioimmunoassay screening tests. The procedure involves extraction of morphine from urine and analysis of its heptafluorobutyryl derivative by gas-liquid chromatography with electron capture detection. Morphine can be determined by this procedure over a range of 0.1-200 microgram/liter of urine, 2 pg of the pure derivative being the lowest amount detectable. Urine samples from patients receiving methadone were analyzed by thin-layer chromatography, radioimmunoassay, and our procedure. The results by our procedure agreed well with those obtained by radioimmunoassay.


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