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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Automated and sensitive determination of four anabolic androgenic steroids in urine by online turbulent flow solid-phase extraction coupled with liquid chromatography-tandem mass spectrometry: A novel approach for clinical monitoring and doping control
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Automated and sensitive determination of four anabolic androgenic steroids in urine by online turbulent flow solid-phase extraction coupled with liquid chromatography-tandem mass spectrometry: A novel approach for clinical monitoring and doping control

机译:在线湍流固相萃取-液相色谱-串联质谱法自动灵敏地测定尿液中四种合成代谢雄激素类固醇:临床监测和兴奋剂控制的新方法

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摘要

A novel method for automated and sensitive analysis of testosterone, androstenedione, methyltestoster-one and methenolone in urine samples by online turbulent flow solid-phase extraction coupled with high performance liquid chromatography-tandem mass spectrometry was developed. The optimization and validation of the method were discussed in detail. The Turboflow C18-P SPE column showed the best extraction efficiency for all the analytes. Nanogram per liter (ng/L) level of AAS could be determined directly and the limits of quantification (LOQs) were 0.01 ng/mL, which were much lower than normally concerned concentrations for these typical anabolic androgenic steroids (AAS) (0.1 ng/mL). The linearity range was from the LOQ to 100 ng/mL for each compound, with the coefficients of determination (r~2) ranging from 0.9990 to 0.9999. The intraday and interday relative standard deviations (RSDs) ranged from 1.1% to 14.5% (n=5). The proposed method was successfully applied to the analysis of urine samples collected from 24 male athletes and 15 patients of prostate cancer. The proposed method provides an alternative practical way to rapidly determine AAS in urine samples, especially for clinical monitoring and doping control.
机译:建立了在线湍流固相萃取-高效液相色谱-串联质谱联用技术自动,灵敏地分析尿液中睾丸激素,雄烯二酮,甲基睾丸酮和甲烯酮的方法。详细讨论了该方法的优化和验证。 Turboflow C18-P SPE色谱柱对所有分析物均显示出最佳的萃取效率。可以直接确定每升AAS的纳克级(ng / L)含量,定量极限(LOQs)为0.01 ng / mL,远低于这些典型的合成代谢雄激素类固醇(AAS)的正常浓度(0.1 ng / L)。毫升)。每种化合物的线性范围为LOQ至100 ng / mL,测定系数(r〜2)为0.9990至0.9999。日内和日间相对标准偏差(RSD)在1.1%至14.5%之间(n = 5)。所提出的方法已成功地用于分析从24名男运动员和15名前列腺癌患者中收集的尿液样品。所提出的方法提供了另一种实用的方法,可快速测定尿液样品中的AAS,尤其是用于临床监测和兴奋剂控制。

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