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Simultaneous determination of fourteen steroid hormone residues in beef samples by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法同时测定牛肉样品中的十四种类固醇激素残留

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A liquid chromatography-tandem mass spectrometry method was developed for the simultaneous determination of 14 steroid hormone residues (hydrocortisone (H), testosterone (T), dehydroepiandrosterone (DHEA), epitestosterone (EpiT), etiocholanolone (E), androsterone (A), progesterone (P), testosterone propionate (TP), pregnanediol (PD), pregnanetriol (PT), estriol (E3), ?±/?2-estradiol (?±/?2-E) and estrone (E1)) in beef samples. Sample preparation and chromatographic conditions were optimized to minimize matrix effects. The beef samples were enzymatically digested with ?2-glucuronidase/arylsulfatase, treated by oscillation and ultrasonic-assisted extraction with acetonitrile. NaCl was added to the crude extract to induce separation of water and acetonitrile layers. After centrifugation and evaporation, the extract was further treated with ZnCl2 to remove lipids and purified by solid phase extraction using LC-C18, LC-Si and LC-NH2 cartridges. The analytes were separated using Poroshell (glucocorticoid, androgen and progestin) and Hydrosphere (estrogen) C18 columns with gradient elution using acetonitrile and water mobile phases. Finally, the eluents were qualitatively and quantitatively determined by electrospray ionization tandem mass spectrometry in multiple reaction monitoring mode. Using a matrix matched external standard method, good linearity in response was obtained with correlation coefficients larger than 0.999. The detection limits of the method were about 0.004a€“0.24 ??g kga?’1 and the quantification limits were 0.016a€“0.84 ??g kga?’1. At the spike levels of 1.0, 2.0 and 4.0 ??g kga?’1 for DHEA, E, A, PT and PD and 0.2, 0.4 and 1.0 ??g kga?’1 for other drugs, the average recoveries of hormones were within the range of 66.4a€“115.2%, and the relative standard deviations (n = 6) were from 2.2% to 10.2%. The method was successfully used for the determination of 14 hormone residues in beef samples.
机译:开发了一种液相色谱-串联质谱法,用于同时测定14种类固醇激素残基(氢化可的松(H),睾丸激素(T),脱氢表雄酮(DHEA),表睾酮(EpiT),乙胆醇酮(E)和雄甾酮(A)牛肉中的孕酮(P),丙酸睾丸酮(TP),孕烯醇(PD),孕烯醇(PT),雌三醇(E3),α±/α2-雌二醇(α±/α2-E)和雌酮(E1))样品。优化了样品制备和色谱条件,以最大程度降低基质效应。用β2-葡糖醛酸糖苷酶/芳基硫酸酯酶对牛肉样品进行酶消化,通过振荡和超声辅助乙腈提取进行处理。将NaCl添加至粗提取物中以引起水和乙腈层的分离。离心和蒸发后,将萃取液进一步用ZnCl2处理以去除脂质,并使用LC-C18,LC-Si和LC-NH2柱通过固相萃取进行纯化。使用Poroshell(糖皮质激素,雄激素和孕激素)和Hydrosphere(雌激素)C18色谱柱进行分离,并使用乙腈和水流动相进行梯度洗脱。最后,通过电喷雾电离串联质谱在多反应监测模式下定性和定量地确定洗脱液。使用矩阵匹配外标法,可获得良好的线性响应,相关系数大于0.999。该方法的检出限约为0.004a·“ 0.24 g·g·kg·a-1”,定量限为0.016a·“ 0.84 g·g·kg·a-1”。在DHEA,E,A,PT和PD的峰值水平分别为1.0、2.0和4.0?g kga?'1和其他药物的0.2、0.4和1.0?g kga?'1的情况下,激素的平均回收率为在66.4a-115.2%的范围内,相对标准偏差(n = 6)在2.2%至10.2%之间。该方法已成功用于牛肉样品中14种激素残留的测定。

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