Detection of Stanozolol and Its Major Metabolites in Human Urine by Liquid Chromatography-Tandem Mass Spectrometry
被引:0
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作者:
M. Thevis
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
M. Thevis
G. Fußhöller
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
G. Fußhöller
H. Geyer
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
H. Geyer
G. Rodchenkov
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
G. Rodchenkov
U. Mareck
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
U. Mareck
G. Sigmund
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
G. Sigmund
A. Koch
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
A. Koch
A. Thomas
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
A. Thomas
W. Schänzer
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机构:German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
W. Schänzer
机构:
[1] German Sport University Cologne,Institute of Biochemistry, Center for Preventive Doping Research
[2] Moscow Anti-Doping Centre,undefined
来源:
Chromatographia
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2006年
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64卷
关键词:
Column liquid chromatography;
Anabolic agents;
Doping in sports;
Stanozolol;
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学科分类号:
摘要:
The determination of stanozolol and its metabolites in human urine has been of particular interest in sports drug testing due to its frequently revealed misuse. A simple and rapid sample preparation procedure based on consecutive solid-phase and liquid–liquid extraction with subsequent re-extraction followed by liquid chromatography and electrospray ionization tandem mass spectrometry was established. It allowed the determination of stanozolol and its metabolic products 16β-OH-stanozolol and 4β-OH-stanozolol in human urine at detection limits of 0.1, 0.2 and 0.2 ng mL−1, respectively, with recoveries ranging from 5 to 38%. The robust nature of the assay and the efficient removal of interfering biological matrix provides excellent signal-to-noise ratios, and, thus, a rapid alternative to established procedures utilizing multiple solid-phase extraction or immunoaffinity chromatography strategies. More than 15 doping control urine specimens tested positive for stanozolol during the last 12 months have been confirmed using the described approach.