Analysis of Veterinary Growth Promoters in Airborne Particulate Matter by Liquid Chromatography-Tandem Mass Spectrometry

被引:0
|
作者
Blackwell, Brett R. [1 ]
Buser, M. D. [2 ]
Johnson, B. J. [3 ]
Baker, M. [4 ]
Cobb, G. P. [5 ]
Smith, P. N. [1 ]
机构
[1] Texas Tech Univ, Dept Environm Toxicol, Inst Environm & Human Hlth, POB 41163, Lubbock, TX 79416 USA
[2] Oklahoma State Univ, Dept Biosyst & Agr Engn, Stillwater, OK 74078 USA
[3] Dept Anim & Food Sci, Lubbock, TX 79409 USA
[4] Texas Tech Univ, Dept Agr Educ & Commun, Lubbock, TX 79409 USA
[5] Baylor Univ, Dept Environm Sci, Waco, TX 76798 USA
关键词
TRENBOLONE ACETATE; STEROID-HORMONES; ANABOLIC AGENTS; HUMAN URINE; 17-BETA-TRENBOLONE; RUNOFF; 17-ALPHA-TRENBOLONE; METABOLITES; EXTRACTION; TRENDIONE;
D O I
暂无
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Veterinary growth promoters are widely used throughout the United States in livestock production. In beef production, steroid hormones are administered to an estimated 90% of cattle. These include the synthetic steroids trenbolone acetate and melengestrol acetate, as well 17 beta-estradiol. Given the endocrine-modulating activity of steroid growth promoters, a sensitive and reliable analytical method is needed to detect trenbolone, melengestrol acetate, estradiol and related residues in environmental matrices. We have developed a method that incorporates solid phase extraction (SPE) and liquid chromatography-tandem mass spectrometry for the simultaneous determination of trendione, trenbolone, melengestrol acetate, estrone, and estradiol in airborne particulate matter samples. Sample preparation involved liquid-solid extraction followed by cleanup with SPE cartridges. Analytes were separated using reversed-phase liquid chromatography. Utilizing a fast gradient, analysis time was under 11 minutes, but did not provide complete isomeric separation of 17 beta-trenbolone and 17 alpha-trenbolone, or 17 beta-estradiol and 17 alpha-estradiol. Column effluent underwent atmospheric-pressure chemical ionization (APCI) followed by detection using a triple-quadrupole mass spectrometer in SRM mode. The lower limit of quantitation (LLOQ) was <= 0.55 ng/filter for all compounds. Recoveries ranged from 93% - 116%, and coefficient of variation (CV) was <= 16.1% at all spiking levels.
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页码:137 / +
页数:4
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