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棒吸附微萃取(BAμE)在尿液基质中合成代谢类固醇的反兴奋剂控制筛查中的应用。

Application of bar adsorptive microextraction (BAμE) for anti-doping control screening of anabolic steroids in urine matrices.

作者信息

Ahmad S M, Almeida C, Neng N R, Nogueira J M F

机构信息

University of Lisbon, Faculty of Sciences, Chemistry and Biochemistry Department, Centre of Chemistry and Biochemistry, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal.

University of Lisbon, Faculty of Sciences, Chemistry and Biochemistry Department, Centre of Chemistry and Biochemistry, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Oct 15;969:35-41. doi: 10.1016/j.jchromb.2014.07.040. Epub 2014 Aug 4.

Abstract

This study proposes a new analytical methodology for the determination of trace levels of testosterone (T) and epitestosterone (E) in urine matrices using bar adsorptive microextraction combined with liquid desorption followed by high-performance liquid chromatography with diode array detection (BAμE-LD/HPLC-DAD). The comparison of different sorbent coatings (five activated carbons, one styrene-divinylbenzene, two modified pyrrolidone, one ciano and one n-vinylpyrrolidone polymers) through BAμE showed that the latter phase presented much higher selectivity and capacity offering multiple mechanisms of interaction. Assays using this phase were performed on 25mL of water samples spiked at the 8.0μg/L level, yielded average recoveries of 92.1 and 93.4% for T and E, respectively, under optimized experimental conditions; BAμE (n-vinylpyrrolidone): 16h (1000rpm), pH 5.5; LD: acetonitrile, 30min under sonication treatment. From the developed analytical methodology, suitable detection limits were achieved (0.4μg/L) and good linear dynamic ranges (1.4-16.0μg/L) with remarkable determination coefficients (r(2)>0.9978). By using the standard addition methodology, the application of the present analytical approach on urine samples revealed good sensitivity. The proposed method, which operated under the floating sampling technology, proved to be a suitable sorption-based static microextraction alternative for screening T, E and the T/E ratio in urine samples for doping control purposes. The methodology showed to be easy to implement, demonstrating good reproducibility, sensitivity and robustness, allowing the possibility to choose the most selective sorbent coating according to the compounds of interest.

摘要

本研究提出了一种新的分析方法,用于测定尿液基质中痕量的睾酮(T)和表睾酮(E),该方法采用棒状吸附微萃取结合液体解吸,随后进行高效液相色谱-二极管阵列检测(BAμE-LD/HPLC-DAD)。通过BAμE对不同的吸附剂涂层(五种活性炭、一种苯乙烯-二乙烯基苯、两种改性吡咯烷酮、一种氰基和一种N-乙烯基吡咯烷酮聚合物)进行比较,结果表明后一种涂层具有更高的选择性和容量,提供了多种相互作用机制。在优化的实验条件下,使用该涂层对25mL加标至8.0μg/L水平的水样进行分析,T和E的平均回收率分别为92.1%和93.4%;BAμE(N-乙烯基吡咯烷酮):16小时(1000转/分钟),pH 5.5;LD:乙腈,超声处理30分钟。从所开发的分析方法中,获得了合适的检测限(0.4μg/L)和良好的线性动态范围(1.4-16.0μg/L),测定系数显著(r(2)>0.9978)。通过使用标准加入法,本分析方法在尿液样本上的应用显示出良好的灵敏度。所提出的方法在浮动采样技术下运行,被证明是一种适用于筛选尿液样本中T、E和T/E比值以进行兴奋剂检测的基于吸附的静态微萃取方法。该方法易于实施,具有良好的重现性、灵敏度和稳健性,允许根据感兴趣的化合物选择最具选择性的吸附剂涂层。

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