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Clinical Chemistry, Vol 11, 1009-1018, Copyright © 1965 by the American Association for Clinical Chemistry
1 Division of Hormone Chemistry, Wesley Medical Research Foundation, Wesley Medical Center, Wichita 14, Kan.
In the course of evaluating urinary 17-ketosteroid (17-KS) gas-liquid chromatographic patterns, a number of peaks with retention times shorter than that of 17-KS were constantly observed. This background material was found to be degradation products of 17-KS produced by HCI hydrolysis. A study with pure 17-KS as a mixture and as individual steroids was used to identify the steroids responsible for most of the 9 compounds with retention times less than etiocholanolone. Hydrolysis in ethyl acetate containing perchloric acid produced smaller amounts of degradation products than HCI-hydrolysis. Enzymatic hydrolysis appears to be the most acceptable system for preparation of the extracts from urine for this system of assay.
Submitted on May 10, 1965
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