Fluorometric Determination of Plasma 11-Hydroxycorticosteroids. II. Studies on the Specificity of the Method

1973 ◽  
Vol 19 (7) ◽  
pp. 718-724 ◽  
Author(s):  
Luis E Mejer ◽  
Roberta C Blanchard

Abstract We have investigated the specificity of the fluorometric method we proposed [Clin. Chem. 19, 710 (1973)] for plasma or serum 11-hydroxycorticosteroid determinations. The principal specific fluorogenic contaminants in the cortisol-containing extract of plasma, as detected by thin-layer chromatography and chemically, were triglycerides and total cholesterol. These contaminants contributed an average of 1.6 µg/dl to the total normal cortisol value. Fatty acids were also found, but did not fluoresce. Nonspecific serum fluorogens were quantitated at 1.3 ± 1.2 µg/dl. Cortisol, corticosterone, and fluorogenic contaminants represented an average of 62.0, 29.1, and 9.9%, respectively, of the total fluorometric plasma cortisol value obtained (expressed in terms of cortisol standard). A ratio of 8.3 ± 2.4 was found for cortisol/corticosterone when each component was determined in terms of its respective standard. Fluorescence scans of the plasma cortisol extract indicated cortisol to be the main component present, accompanied by minor fluorescent contaminants.

Author(s):  
G. F. Read ◽  
Diana R. Fahmy ◽  
R. F. Walker

A radioimmunoassay for plasma cortisol featuring the gamma-emitting radioligand 125I-iodohistamine, coupled to cortisol-3-(O-carboxymethyl)-oxime, is described. The new procedure retains much of the specificity associated with the use of anti-cortisol-3-BSA sera with tritium-labelled radioligands, and has the further advantages that running costs are lower and there is a greater potential for automation. Cortisol values obtained by this procedure agree well with those obtained by a published specific radioimmunoassay using the tritiated cortisol radioligand. Specificity of the procedure was checked by comparing values obtained with and without thin-layer chromatography purification: correlation was excellent (r = 0·96). Satisfactory levels of sensitivity, precision, and accuracy were obtained.


1980 ◽  
Vol 63 (4) ◽  
pp. 864-868
Author(s):  
Harris H Wisneski

Abstract The preservative cis-l-(3-chloroallyl)-3,5,7- triaza-1-azoniaadamantane chloride (quaternium-15) was detected and differentiated from other formaldehyde-releasing preservatives such as 2-bromo-2-nitropropane-l,3-diol, l-hydroxymethyl-5,5-dimethylhydantoin, and imidazolidinyl urea in cosmetics by thin layer chromatography. A minimum of 0.1 μg quaternium-15 was detected by fluorescence of the lutidine derivative formed from a buffered 2,4-pentanedione indicator spray and formaldehyde liberated from this preservative. Another indicator spray, a modified Dragendorf reagent, provided additional confirmation at lower sensitivity. The fluorometric determination of quaternium-15 was based on its quantitative release of formaldehyde to form the fluorescent 3,5-diacetyl-1,4-dihydrolutidine. Close to the theoretical value of 6 moles of formaldehyde per mole of quaternium-15 was verified experimentally (5.8–6.3). Average recoveries of quaternium-15 from a bath oil and lotion ranged from 91.7 to 103%.


2019 ◽  
Vol 11 (14) ◽  
pp. 1891-1897 ◽  
Author(s):  
Fabien Robert-Peillard ◽  
Elodie Mattio ◽  
Aïnhoa Komino ◽  
Jean-Luc Boudenne ◽  
Bruno Coulomb

In this paper, a new thin-layer chromatography (TLC) method for the determination of individual volatile fatty acids (VFAs) is presented.


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