Literature DB >> 15905063

Enzymic conversion of 3beta-hydroxy-5-ene-steroids and their sulfates to 3-oxo-4-ene-steroids for increasing sensitivity in LC-APCI-MS.

Tatsuya Higashi1, Naoki Takayama, Kazutake Shimada.   

Abstract

A method of increasing the sensitivity of 3beta-hydroxy-5-ene (Delta5)-steroids in liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry (LC-APCI-MS) based on the structural conversion by cholesterol oxidase (ChO) was demonstrated. The Delta5-steroids were rapidly converted to their 3-oxo-4-ene (Delta4)-forms by the treatment with ChO and the obtained Delta4-forms provided 3-14-fold higher sensitivity compared to intact steroids in the positive-APCI-MS. This enzymic conversion method was also applied to the sulfated conjugates of Delta5-steroids after solvolysis. The method enabled the detection of trace levels of dehydroepiandrosterone and androstenediol 3-sulfate in human serum, which could not be detected by the usual LC-MS.

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Year:  2005        PMID: 15905063     DOI: 10.1016/j.jpba.2005.04.005

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  2 in total

1.  Novel fragmentation pathways of anionic adducts of steroids formed by electrospray anion attachment involving regioselective attachment, regiospecific decompositions, charge-induced pathways, and ion-dipole complex intermediates.

Authors:  Nalaka S Rannulu; Richard B Cole
Journal:  J Am Soc Mass Spectrom       Date:  2012-06-26       Impact factor: 3.109

2.  New cytotoxic steroid from Stachyurus imalaicus var. himalaicus.

Authors:  Yun-Song Wang; Jing-Hua Yang; Shi-De Luo; Hong-Bin Zhang; Liang Li
Journal:  Molecules       Date:  2007-03-17       Impact factor: 4.411

  2 in total

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