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  • Analytical approach for the determination of steroid profile of humans by gas chromatography isotope ratio mass spectrometry aimed at distinguishing between endogenous and exogenous steroids.

Analytical approach for the determination of steroid profile of humans by gas chromatography isotope ratio mass spectrometry aimed at distinguishing between endogenous and exogenous steroids.

Journal of pharmaceutical and biomedical analysis (2014-12-17)
Ewa Bulska, Damian Gorczyca, Izabela Zalewska, Andrzej Pokrywka, Dorota Kwiatkowska
ABSTRACT

The contamination of commonly used supplements by unknown steroids as well as their metabolites (parent compounds) become a challenge for the analytical laboratories. Although the determination of steroids profile is not trivial because of the complex matrix and low concentration of single compound, one of the most difficult current problem is to distinguish, during analytical procedure, endogenous androgens such as testosterone, dehydrotestosterone or dehydroepiandrosterone from their synthetic equivalents. The aim of this work was to develop and validate an analytical procedure for determination of the steroid profile in human urine by gas chromatography-combustion-isotope ratio mass spectrometry (GC/C/IRMS) toward distinguishing between endogenous and exogenous steroids. Beside the optimization of the experimental parameters for gas chromatography separation and mass spectrometry, attention was focused on urine sample preparation. Using an optimized sample preparation protocol it was possible to achieve better chromatographic resolutions and better sensitivity enabling the determination of 5 steroids, androsterone, etiocholanolone, testosterone, 5-androstandiol, 11-hydroxyandrdostane, pregnandiol, with the expanded uncertainty (k=2) below 1‰. This enable to evaluate the significant shift of the δ(13)C/(12)C [‰] values for each of examined steroids (excluding ERC). The analytical protocol described in this work was successfully used for the confirmation of positive founding urine by evaluation T/E ratio after GC/C/IRMS analysis.

MATERIALS
Product Number
Brand
Product Description

Ethanol solution, certified reference material, 2000 μg/mL in methanol
Ethanol standards 10% (v/v), 10 % (v/v) in H2O, analytical standard
5α-Androstane
Methanol, purification grade, 99.8%
Supelco
Testosterone solution, 1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®
Supelco
Androsterone, VETRANAL®, analytical standard
Methanol, ACS spectrophotometric grade, ≥99.9%
Methanol, ACS reagent, ≥99.8%
Methanol, ACS reagent, ≥99.8%
Methanol, analytical standard
Methanol, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8% (GC)
Methanol, anhydrous, 99.8%
Methanol, puriss., meets analytical specification of Ph Eur, ≥99.7% (GC)
Methanol, BioReagent, ≥99.93%
Methanol, suitable for HPLC, ≥99.9%
Methanol, HPLC Plus, ≥99.9%
Methanol, Laboratory Reagent, ≥99.6%
Methanol, suitable for HPLC, gradient grade, ≥99.9%
Methanol, suitable for HPLC, gradient grade, suitable as ACS-grade LC reagent, ≥99.9%
Ethyl alcohol, Pure 190 proof, for molecular biology
Ethanol Fixative 80% v/v, suitable for fixing solution (blood films)
trans-Dehydroandrosterone, ≥99%
Supelco
Testosterone, VETRANAL®, analytical standard
Dehydrated Alcohol, Pharmaceutical Secondary Standard; Certified Reference Material
USP
Dehydrated Alcohol, United States Pharmacopeia (USP) Reference Standard
Methanol, Pharmaceutical Secondary Standard; Certified Reference Material
Methanol, ACS reagent, ≥99.8%
Methanol solution, contains 0.50 % (v/v) triethylamine
Ethyl alcohol, Pure, 200 proof
Ethanol, tested according to Ph. Eur.