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高效液相色谱-串联质谱法快速分析牛组织中的 19 种同化类固醇

Fast analysis of 19 anabolic steroids in bovine tissues by high performance liquid chromatography with tandem mass spectrometry.

机构信息

Department of Pharmacology and Toxicology, National Veterinary Research Institute, Pulawy, Poland.

出版信息

J Sep Sci. 2019 Nov;42(21):3319-3329. doi: 10.1002/jssc.201900494. Epub 2019 Sep 18.

Abstract

For the detection of 19 steroid hormones in bovine muscle, a fast and sensitive liquid chromatography with electrospray ionization tandem mass spectrometry method was developed using both positive and negative ionization mode. Chromatographic separation on Poroshell 120-EC C18 column was achieved in less than 10 min using isocratic elution of mobile phase of acetonitrile/methanol/water. The compounds were extracted from muscle tissue using ethyl acetate and quick, easy, cheap, effective, rugged, and safe technique. The purification of the obtained extract was performed by dispersive solid-phase extraction with sorbents C18, primary secondary amine and magnesium sulphate. The method was validated in accordance with the Commission Decision 2002/657/EC. For all steroids tested good recoveries were obtained (from 51.2 to 121.4%) in the concentration range from decision limits until 5 µg/kg. The values of decision limits and the detection capabilities for individual compounds were in the range 0.10-0.48 and 0.17-0.95 µg/kg, respectively. The method was characterized by satisfactory linearity for most compounds (correlation coefficients > 0.99) and the reproducibility was lower than 35%. The elaborated procedure has met the criteria for confirmatory methods and is currently used in the official control of hormones.

摘要

为了检测牛肌肉中的 19 种甾体激素,建立了一种基于电喷雾串联质谱的正、负离子同时检测的快速、灵敏的液相色谱分析方法。采用 Poroshell 120-EC C18 柱,在 10 min 内,以乙腈/甲醇/水为流动相,采用等度洗脱的方式实现了化合物的色谱分离。采用乙酸乙酯和快速、简单、便宜、有效、耐用、安全(QuEChERS)技术从肌肉组织中提取化合物。用 C18、伯仲胺和硫酸镁作为吸附剂,通过分散固相萃取对提取的粗提物进行净化。该方法符合欧盟委员会第 2002/657/EC 号决定进行了验证。在所测试的所有类固醇中,在从检测限到 5 µg/kg 的浓度范围内,均获得了良好的回收率(51.2%至 121.4%)。各个化合物的检测限和检测能力值分别在 0.10-0.48 和 0.17-0.95 µg/kg 范围内。该方法对大多数化合物具有令人满意的线性(相关系数 >0.99),重现性低于 35%。所建立的方法符合确证方法的标准,目前已用于激素的官方检测。

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