Gas-Liquid Chromatography-Mass Spectroscopy Determination of Clopamide in Plasma

1989 ◽  
Vol 78 (8) ◽  
pp. 679-682 ◽  
Author(s):  
Wolfgang Stüber ◽  
Henning Blume ◽  
Fritz Sörgel ◽  
Gerd Stenzhorn
1975 ◽  
Vol 58 (3) ◽  
pp. 582-584
Author(s):  
Glenn E Martin ◽  
Peter C Buscemi ◽  
Boyd B Butts

Abstract Liquid-liquid extraction was carried out prior to gas-liquid chromatographic (GLC) determination of amyl and isoamyl acetate in alcoholic beverages. The concentrations of amyl acetate and isoamyl acetate ranged from 4 to 29 and 2.5 to 322 ppm, respectively. Recovery studies for isoamyl and amyl acetate were carried out; these compounds were recovered at 90 and 92%, respectively. A liquid-liquid extraction also was carried out prior to the GLC determination of benzaldehyde. When chloroform was used in the liquid extraction, the results obtained by the GLC procedure compared favorably in most cases with those obtained by the ultraviolet spectrophotometric procedure. In the GLC method the benzaldehyde varied from 5 to 150 ppm for both imported and natural wines. The compounds in the effluent from the chromatograph, namely, amyl acetate, isoamyl acetate, and benzaldehyde, were confirmed by mass spectroscopy.


1971 ◽  
Vol 67 (2) ◽  
pp. 303-315 ◽  
Author(s):  
A. J. Moolenaar ◽  
A. P. van Seters

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.


1992 ◽  
Author(s):  
Ronald L. Shippee ◽  
Avery A. Johnson ◽  
William G. Cioffi ◽  
James Lasko ◽  
Thomas E. LeVoyer

1972 ◽  
Vol 55 (4) ◽  
pp. 840-845 ◽  
Author(s):  
Charles R Midkiff ◽  
Willard D Washington

Techniques developed for use with gas-liquid chromatography for the examination of evidence collected at the scene of suspected arson fires and firebombings are discussed. Both solvent extraction and vapor phase examinations are employed. Internal standards are used for the identification of specific components in actual samples to allow confirmation of hydrocarbon type, e.g., gasoline and kerosene. Operating parameters and solvent selection criteria are included. Results obtained from known materials and residual hydrocarbons in actual samples are compared.


1977 ◽  
Vol 60 (1) ◽  
pp. 56-59 ◽  
Author(s):  
Emil Weisenberg ◽  
Baruch Gershon ◽  
Judith Schoenberg

Abstract A rapid and specific method is described for the determination of microamounts of methyl, propyl, and butyl p-hydroxybenzoic esters (parabens) in pharmaceuticals and cosmetics. The method involves the direct extraction of parabens into benzene or chloroform followed by derivatization with phosphorochloridate. The diethyl phosphate ester derivatives are cleaned up on a Florisil minicolumn and finally measured by gas-liquid chromatography on 5% OV-210 on Gas-Chrom Q. A flame photometric detector or a KCl thermionic detector may be used. The concentration response was linear up to 40 ng parabens. The reproducibility and margin of error were tested with fortified samples. This method may be applied to the estimation of other phenol derivatives.


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