Simultaneous determination of thirteen different steroid hormones using micro UHPLC-MS/MS with on-line SPE system

被引:32
|
作者
Marta, Zoltan [1 ,2 ]
Bobaly, Balazs [3 ]
Fekete, Jeno [2 ]
Magda, Balazs [1 ]
Imre, Timea [1 ]
Meszaros, Katalin Viola [4 ]
Balint, Maria [5 ]
Szabo, Pal Tamas [1 ]
机构
[1] Hungarian Acad Sci, Res Ctr Nat Sci, MS Metabol Lab, Core Facil, Magyar Tudosok Blvd 2, H-1117 Budapest, Hungary
[2] Budapest Univ Technol & Econ, Fac Chem Technol & Biotechnol, Dept Inorgan & Analyt Chem, Szent Gellert Sq 4, H-1111 Budapest, Hungary
[3] Univ Lausanne, Univ Geneva, Ctr Med Univ CMU, Sch Pharmaceut Sci, Rue Michel Servet 1, CH-1206 Geneva, Switzerland
[4] Semmelweis Univ, Hungarian Acad Sci, Momentum Hereditary Endocrine Tumours Res Grp, Szentkiralyi St 46, H-1088 Budapest, Hungary
[5] Balint Analika Ltd, Fehervari St 144, H-1116 Budapest, Hungary
关键词
LC-MS/MS; Steroid hormone; Microflow liquid chromatography; On-line SPE; TANDEM MASS-SPECTROMETRY; LC-MS/MS; HUMAN SERUM; SIMULTANEOUS QUANTIFICATION; HUMAN HAIR; REFERENCE INTERVALS; HUMAN PLASMA; CORTISOL; TESTOSTERONE; VALIDATION;
D O I
10.1016/j.jpba.2017.12.014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ultratrace analysis of sample components requires excellent analytical performance in terms of limits of quantitation (LOQ). Micro UHPLC coupled to sensitive tandem mass spectrometry provides state of the art solution for such analytical problems. Using on-line SPE with column switching on a micro UHPLC-MS/MS system allowed to decrease LOQ without any complex sample preparation protocol. The presented method is capable of reaching satisfactory low LOQ values for analysis of thirteen different steroid molecules from human plasma without the most commonly used off-line SPE or compound derivatization. Steroids were determined by using two simple sample preparation methods, based on lower and higher plasma steroid concentrations. In the first method, higher analyte concentrations were directly determined after protein precipitation with methanol. The organic phase obtained from the precipitation was diluted with water and directly injected into the LC-MS system. In the second method, low steroid levels were determined by concentrating the organic phase after steroid extraction. In this case, analytes were extracted with ethyl acetate and reconstituted in 90/10 water/acetonitrile following evaporation to dryness. This step provided much lower LOQs, outperforming previously published values. The method has been validated and subsequently applied to clinical laboratory measurement. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:258 / 267
页数:10
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