Abstract: A method to quantify metabolites of 17beta-nandrolone (17betaN) in boar and horse urine has been optimized and validated. Metabolites excreted in free form were extracted at pH 9.5 with tert-butylmethylether. The aqueous phases were applied to Sep Pak C18 cartridges and conjugated steroids were eluted with methanol. After evaporation to dryness, either enzymatic hydrolysis with beta-glucuronidase from Escherichia coli or solvolysis with a mixture of ethylacetate:methanol:concentrated sulphuric acid were applied to the extract. Deconjugated steroids were then extracted at alkaline pH with tert-butylmethylether. The dried organic extracts were derivatized with MSTFA:NH4I:2-mercaptoethanol to obtain the TMS derivatives, and were subjected to analysis by gas chromatography mass spectrometry (GC/MS). The procedure was validated in boar and horse urine for the following metabolites: norandrosterone, noretiocholanolone, norepiandrosterone, 5beta-estran-3alpha, 17beta-diol, 5alpha-estran-3beta, 17beta-diol, 5alpha-estran-3beta, 17alpha-diol, 17alpha-nandrolone, 17betaN, 5(10)-estrene-3alpha, 17alpha-diol, 17alpha-estradiol and 17beta-estradiol in the different metabolic fractions. Extraction recoveries were higher than 90% for all analytes in the free fraction, and better than 80% in the glucuronide and sulphate fractions, except for 17alpha-estradiol in the glucuronide fraction (74%), and 5alpha-estran-3beta, 17alpha-diol and 17betaN in the sulphate fraction (close to 70%). Limits of quantitation ranged from 0.05 to 2.1 ng mL(-1) in the free fraction, from 0.3 to 1.7 ng mL(-1) in the glucuronide fraction, and from 0.2 to 2.6 ng mL(-1) in the sulphate fraction. Intra- and inter-assay values for precision, measured as relative standard deviation, and accuracy, measured as relative standard error, were below 15% for most of the analytes and below 25%, for the rest of analytes. The method was applied to the analysis of urine samples collected after administration of 17betaN laureate to boars and horses, and its suitability for the quantitation of the metabolites in the three fractions has been demonstrated.
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This study details a method for measuring metabolites of 17beta-nandrolone in boar and horse urine. The method was validated and applicable to analyze urine samples collected after administration of 17beta-nandrolone laureate to boars and horses.
Objective of the Study
The objective of this research was to validate and optimize a method for quantifying metabolites of 17beta-nandrolone in boar and horse urine. The method capitalizes on gas chromatography-mass spectrometry to identify these metabolites.
Methodology
Metabolites in free form were extracted using tert-butylmethylether at pH 9.5 from the urine samples.
The aqueous phases were then applied to Sep Pak C18 cartridges and eluted with methanol. Enzymatic hydrolysis or solvolysis was applied to the extract after evaporation.
The steroids were deconjugated and once again extracted using tert-butylmethylether, but this time at an alkaline pH.
The dried organic extracts were derivatized and analysed using gas chromatography mass spectrometry (GC/MS).
Intra- and inter-assay precision and accuracy were measured, and this method was applied to urine samples collected after giving 17beta-nandrolone laureate to boars and horses.
Results
The extraction recoveries were generally above 80%, with the highest extraction recoveries observed from the free fraction (above 90%) and the lowest seen in the sulfate fraction (close to 70% for some analytes).
The quantification limits varied depending on the fraction, with the lowest limit of quantitation found in the free fraction (from 0.05 to 2.1 ng mL(-1)).
Intra- and inter-assay values for precision were below 15% for most of the analytes and below 25% for the rest.
It was found that this method could be used to quantify the metabolites in the three fractions from urine samples collected after administering 17beta-nandrolone laureate to boars and horses.
Cite This Article
APA
Roig M, Segura J, Ventura R.
(2006).
Quantitation of 17beta-nandrolone metabolites in boar and horse urine by gas chromatography-mass spectrometry.
Anal Chim Acta, 586(1-2), 184-195.
https://doi.org/10.1016/j.aca.2006.08.033
Unitat de Recerca en Farmacologia, Institut Municipal d'Investigacuó Mèdica, Dr. Aiguader, 80, 08003 Barcelona, Spain.
Segura, Jordi
Ventura, Rosa
MeSH Terms
Anabolic Agents / chemistry
Animals
Cattle
Chemistry Techniques, Analytical / methods
Escherichia coli / enzymology
Esters / chemistry
Gas Chromatography-Mass Spectrometry / methods
Glucuronidase / chemistry
Glucuronides / chemistry
Horses
Hydrogen-Ion Concentration
Methanol / chemistry
Nandrolone / analysis
Nandrolone / urine
Steroids / chemistry
Sus scrofa
Citations
This article has been cited 3 times.
Dołowy M, Pyka-Pająk A, Jampílek J. Simple and Accurate HPTLC-Densitometric Method for Assay of Nandrolone Decanoate in Pharmaceutical Formulation. Molecules 2019 Jan 25;24(3).
Iwona MŻ, Barbara W, Alicja K, Sebastian W, Katarzyna S, Andrzej P. Control of Anabolic Hormone Residues in Tissues of Slaughter Animals in Poland During the Period of 2011-2015. J Vet Res 2017 Mar;61(1):69-79.
Jiang JQ, Zhang L, Li GL, Zhang HT, Yang XF, Liu JW, Li RF, Wang ZL, Wang JH. Analysis of 19-nortestosterone residue in animal tissues by ion-trap gas chromatography-tandem mass spectrometry. J Zhejiang Univ Sci B 2011 Jun;12(6):460-7.