Rapid qualitative procedure for the identification of petroleum products in animal tissue by gas-liquid chromatography

1979 ◽  
Vol 22 (1) ◽  
pp. 285-286 ◽  
Author(s):  
L. L. Zinn ◽  
W. C. Edwards
Keyword(s):  
Liquid Chromatography ◽  
Petroleum Products ◽  
Animal Tissue ◽  
Gas Liquid Chromatography

Hydrocarbons in Eastern Canadian Marine Waters Determined by Fluorescence Spectroscopy and Gas–Liquid Chromatography

1977 ◽  
Vol 34 (3) ◽  
pp. 347-353 ◽  
Author(s):  
P. D. Keizer ◽  
D. C. Gordon Jr. ◽  
J. Dale
Keyword(s):  
Liquid Chromatography ◽  
Fluorescence Spectroscopy ◽  
Key Words ◽  
Petroleum Products ◽  
Gas Liquid Chromatography ◽  
Marine Waters ◽  
Northwest Atlantic ◽  
Oil Hydrocarbons ◽  
Contour Plots

Concentrations of n-alkanes ranged from <20 ng/ℓ to about 1 μg/ℓ at depths of 2 and 50 m. Estimated oil concentrations based on fluorescence analyses ranged from 0.2 to 9.3 μg/ℓ. The highest concentrations occurred in Bedford Basin; the similarity of fluorescence contour plots to petroleum products and the presence of unresolved envelopes in chromatograms suggest that a large portion of the hydrocarbons in the Basin are derived from oil. Hydrocarbons in other regions appear to be principally biogenic in origin. Key words: Oil detection, northwest Atlantic, gas–liquid chromatography, fluorescence spectroscopy

Sensitive and Specific Gas-Liquid Chromatographic-Spectrophotometric Screening Procedure for Trace Levels of Five Sulfonamides in Liver, Kidney, and Muscle Tissue

1978 ◽  
Vol 61 (5) ◽  
pp. 1050-1053
Author(s):  
Donald P Goodspeed ◽  
Randy M Simpson ◽  
Raymond B Ashworth ◽  
Jerry W Shafer ◽  
Henry R Cook
Keyword(s):  
Liquid Chromatography ◽  
Electron Capture ◽  
Muscle Tissue ◽  
Ethyl Ether ◽  
Methylene Chloride ◽  
Animal Tissue ◽  
Gas Liquid Chromatography ◽  
Separatory Funnel ◽  
Liquid Chromatographic ◽  
Ppm Level

Abstract Free and conjugated sulfonamides are extracted from edible animal tissue with acetone. Carbohydrate "is precipitated and removed, and the acetone is evaporated. The residue is transferred to a separatory funnel with ethyl ether and 17V HC1. The acid layer is drawn off and a portion of the 17V HC1 is screened, using the Bratton-Marshall reaction. If this portion is positive, the remaining portion is buffered to pH 6.5 and extracted with methylene chloride. The residue is methylated with diazomethane and then acylated with pentafluoropropionic anhydride. The resulting derivatives are detected by gas-liquid chromatography, using electron capture (63Ni) detection and a column packed with 3% OV-17 on Gas-Chrom Q. This method has been validated by recovering sulfathiazole, sulfachloropyrazine, sulfamethazine, sulfadimethoxine, and sulfabromomethazine from liver, kidney, and muscle at levels of 0.1, 0.5, and 1.0 ppm. The 5 sulfonamides were recovered in excess of 60%, with an average mean recovery of 81.5% at the 0.1 ppm level, 79.1% at the 0.5 ppm level, and 76.0% at the 1.0 ppm level.

A study of asphalt-aggregate interactions using inverse gas-liquid chromatography

1974 ◽  
Vol 24 (11) ◽  
pp. 645-654 ◽  
Author(s):  
F. Alan Barbour ◽  
Richard V. Barbour ◽  
J. Claine Peterson
Keyword(s):  
Liquid Chromatography ◽  
Gas Liquid Chromatography

GASCHROMATOGRAPHIC DETERMINATION OF STEROIDS IN THE URINE OF PATIENTS WITH CUSHING'S SYNDROME

1971 ◽  
Vol 67 (2) ◽  
pp. 303-315 ◽  
Author(s):  
A. J. Moolenaar ◽  
A. P. van Seters
Keyword(s):  
Liquid Chromatography ◽  
Cushing’S Syndrome ◽  
Normal Subjects ◽  
Diagnostic Value ◽  
Cushing's Syndrome ◽  
Gas Liquid Chromatography ◽  
Obese Subjects

ABSTRACT The 17-oxosteroids were estimated in the urine of 27 patients with Cushing's syndrome by gas-liquid chromatography (G. L. C.). The values of the various steroid fractions are compared with those of normal subjects, patients with thyrotoxicosis and obese subjects. The effect of the age of the patients on the diagnostic value of the invidual 17-oxosteroids and their ratios is discussed.

Simultaneous Determination of Lactulose and Mannitol in Urine of Burn Patients by Gas-Liquid Chromatography

1992 ◽  
Author(s):  
Ronald L. Shippee ◽  
Avery A. Johnson ◽  
William G. Cioffi ◽  
James Lasko ◽  
Thomas E. LeVoyer
Keyword(s):  
Liquid Chromatography ◽  
Simultaneous Determination ◽  
Gas Liquid Chromatography ◽  
Burn Patients

Obtaining and Characterization of Alhagi persarum Boiss. et Buhse Callus Cell Cultures, Isoflavonoid Producers

2020 ◽  
Vol 36 (6) ◽  
pp. 35-48
Author(s):  
D.V. Коchkin ◽  
G.I. Sobolkovа ◽  
А.А. Fоmеnkov ◽  
R.А. Sidorov ◽  
А.М. Nоsоv
Keyword(s):  
Fatty Acids ◽  
Cell Culture ◽  
Liquid Chromatography ◽  
Secondary Metabolites ◽  
Cell Cultures ◽  
Mass Spectrometric ◽  
Mass Spectrometric Detection ◽  
Gas Liquid Chromatography ◽  
Callus Cell

The physiological characteristics of the callus cell cultures of Alhagi persarum Boiss et Buhse, a member of the legume family, widely used in folk medicine, have been studied. It was shown that the source of the explant was an important factor in the initiation of callusogenesis: more intense callusogenesis (almost 100%) was observed for explants from various organs of sterile seedlings, rather than intact plants (less than 30%). As a result, more than 20 lines of morphologically different callus cell cultures were obtained, and the growth parameters for the 5 most intensively growing lines were determined. The composition of fatty acids (FA) of total lipids and secondary metabolites in the most physiologically stable callus line Aр-207 was analyzed. Using capillary gas-liquid chromatography with mass spectrometric detection (GLC-MS), 19 individual C12--C24 FAs were identified, the main fraction of which were palmitic (~ 23%), stearic (~ 22%), linoleic (~ 14%) and α-linolenic (~ 33%) acids. The established atypical ratio of FAs (a simultaneous high content of both saturated FAs and polyunsaturated α-linolenic acid) is possibly due to the adaptation of cells to in vitro growth conditions. Phytochemical analysis of the secondary metabolites was carried out using ultra-performance liquid chromatography with electrospray ionization mass spectrometric detection (UPLC MS). Compounds belonging to different structural groups of isoflavones were found. Aglycones (calycosin, formononetin and afrormosin isomer), glucosides (formononetin glucoside), as well as esters of glucosides (malonylglycosides of calicosin, formononetin, afrormosin isomers, glycitein and genistein) were detected. These secondary metabolites are widespread in plants of the Fabaceae family; however, isoflavones are rare in representatives of the Alhagi genus. The presence of malonylated isoflavone glycosides in Alhagi spp. was shown for the first time. endemic plant species, Alhagi, in vitro cell culture, callus cell culture, isoflavones, fatty acids All studies were carried out using the equipment of the "Experimental Biotechnological Facility" and the "All-Russian Collection of Cell Cultures of Higher Plants" of IРР RAS. This work was supported by the Russian Foundation for Basic Research (RFBR), contract no.18-54-06021 (Az_a), and the Government of the Russian Federation, Megagrant Project no. 075-15-2019-1882.

Sign in / Sign up

Export Citation Format

Share Document