Analysis of some hydroxy fatty compounds as their trimethylsilyl ethers by gas-liquid chromatography

1971 ◽  
Vol 55 (2) ◽  
pp. 402-404 ◽  
Author(s):  
R. Kannan ◽  
A. Rajiah ◽  
M.R. Subbaram ◽  
K.T. Achaya
1969 ◽  
Vol 15 (3) ◽  
pp. 190-196 ◽  
Author(s):  
Robert D Baynton ◽  
Donald J Campbell

Abstract A simplified method for following the urinary excretion of estriol, pregnanediol, and pregnanolone during the course of pregnancy is presented. The procedure has been used successfully in a large hospital laboratory. An important advantage is that the estrogen and progesterone metabolites are measured simultaneously, and separate extraction and gas-liquid chromatography is not required. The urine specimen is hydrolyzed enzymatically, extracted, and the steroids are converted to trimethylsilyl ethers. Temperature-programmed gas-liquid chromatography is carried out on a 2% neopentyl glycol succinate column using a hydrogen flame ionization detector.


1967 ◽  
Vol 54 (1) ◽  
pp. 37-50 ◽  
Author(s):  
Roberto Rivera ◽  
Ralph I. Dorfman ◽  
Enrico Forchielli

ABSTRACT A modified method using gas-liquid chromatography (GLC) is described for the determination of androsterone*, aetiocholanolone, dehydroepiandrosterone, pregnanediol and pregnanetriol in the same urine aliquot. After sequential enzymatic hydrolysis and solvolysis, the urine extract is separated into 3 main fractions by silica gel column chromatography; one containing mainly the 17-ketosteroids, androsterone, aetiocholanolone and dehydroepiandrosterone; a second containing pregnanediol and the third pregnanetriol. After formation of the trimethylsilyl ethers (TMSi), the respective fractions are subjected to gas-liquid chromatography for quantitation. Tritiated androsterone, pregnanediol and pregnanetriol are added prior to extraction of the urines to check for recoveries. The method is specific and reproductible and is sufficiently sensitive to permit determination of urinary steroid excretion levels as low as 0.025 mg/24 hours. Results obtained with this method in the study of normal males and females and various pathological conditions are presented.


1970 ◽  
Vol 47 (1) ◽  
pp. 55-64 ◽  
Author(s):  
H. L. J. MAKIN

SUMMARY The gas-liquid chromatography (GLC) of some C19 steroid formates has been investigated in an attempt to speed up the final stages of the estimation of the 11-oxygenation index. SE-30 was found to give the best separation of the urinary C19 steroids formed after borohydride reduction and periodate oxidation of urine. Formates, acetates, propionates, n-butyrates, valerates and trimethylsilyl ethers were examined; formate esters gave the best separation of androsterone and aetiocholanolone. Estimation of the 11-oxygenation index by GLC increases the specificity and speed of single estimations and it is suggested that this method may find use as a rapid screening test for abnormal urinary steroid patterns.


1975 ◽  
Vol 21 (2) ◽  
pp. 181-185 ◽  
Author(s):  
Clarence M. Paine ◽  
Robert Cherniak

An analytical procedure, using gas–liquid chromatography, was developed for the identification of the per(trimethylsilyl) ethers of the constituent monosaccharides obtained from the capsular polysaccharides of Clostridium perfringens Hobbs 5, Hobbs 9, Hobbs 10, and NCTC 10578. Qualitative and quantitative differences between the major polysaccharide components enabled the differentiation of the four strains of C. perfringens investigated.


1970 ◽  
Vol 48 (12) ◽  
pp. 817-823
Author(s):  
M. P. Stefanovic ◽  
H. S. Bayley ◽  
S. J. Slinger

Two boars were fed normally to 19 weeks of age and then underfed so that their growth was severely restricted. Two other boars were underfed to 19 weeks of age and thus did not grow; they were then normally fed and the experiment was continued until they reached the same weight as the first two boars. The excretion of 17-ketosteroids (17-KS) in the urine of the four boars was measured on 2 days each week by separating their trimethylsilyl ethers by gas–liquid chromatography. The excretion of 17-KS reached a maximum of 9.0 mg per day for the boars which were fed normally in the first part of the experiment. Reducing their allocation of feed did not have an immediate effect on the excretion of total 17-KS, but after 4 weeks the excretion declined to about 1.0 mg per day. The 17-KS excretion of the boars which were underfed initially remained less than 0.5 mg per day, but increased when the feed allocation and hence growth rate of the boars increased. However, the excretion of 17-KS by these boars did not reach the levels recorded for the boars which had grown normally from the start of the experiment.


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