A validated surrogate analyte LC-MS/MS assay for quantification of endogenous cortisol in human whole blood

被引:11
作者
Agrawal, Karan [1 ]
Voggu, Ramakrishna R. [1 ]
Pisek, Daniel [1 ]
Becht, Steven [2 ]
Chudnovskiy, Ross [1 ]
Dufour, Geraldine Mercier [3 ]
Arfvidsson, Cecilia [4 ]
Thomas, C. Eric [1 ]
机构
[1] Covance Labs Inc, 8211 SciCor Dr, Indianapolis, IN 46214 USA
[2] Covance Labs Inc, 3301 Kinsman Blvd, Madison, WI 53704 USA
[3] Covance Labs Inc, Otley Rd, Harrogate HG3 1PY, England
[4] AstraZeneca R&D, Clin Pharmacol & Safety Sci, Quantitat Pharmacol Clin Pharmacol, Gothenburg, Sweden
关键词
Cortisol; Whole blood; LC-MS/MS; Surrogate analyte; Supported liquid extraction; Bioanalysis; TANDEM MASS-SPECTROMETRY; QUANTITATION; AGREEMENT; PLASMA;
D O I
10.1016/j.jpba.2021.114028
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cortisol is a steroid hormone that is frequently measured as a marker of stress, inflammation, and immune function. While commonly analyzed in saliva, hair, blood plasma and urine, a recent trend towards whole blood-based at-home collection devices has emerged, which necessitates development of more sensitive assays for cortisol in whole blood. To support the implementation of a patient-centric sampling approach in a drug development program, a fit-for-purpose surrogate analyte-based liquid chromatography-tandem mass spectrometry (LC-MS/MS) assay for cortisol in whole blood was developed using C-13(3)-cortisol as a surrogate analyte and cortisol-d6 as the internal standard. The surrogate analyte approach was chosen due to a lack of available cortisol-free whole blood and the absence of appropriately representative surrogate matrices. Samples were prepared using supported liquid extraction, and the LC-MS/MS analysis consisted of a 4.00 min analytical run. The method demonstrated linearity between 0.500 and 500 ng/mL of C-13(3)-cortisol, and accuracy, precision and robustness were all acceptable per current regulatory guidance for bioanalytical method validation of chromatographic assays for cortisol- and C-13(3)-cortisol-based quality control (QC) samples when quantified against a C-13(3)-cortisol calibration curve. The acceptable robustness of cortisol-based QCs when quantified against a C-13(3)-cortisol-based calibration curve also suggests parallelism between the analytes. These results indicate a viable surrogate analyte method, that is fit-for-purpose to analyze whole blood cortisol levels using a surrogate analyte LC-MS/MS approach. Evaluation of patient samples showed very promising comparability between whole blood and plasma cortisol concentrations, suggesting that whole blood could be used in place of or in addition to a plasma-based sampling protocol in clinical trials analyzing cortisol. Overall, this method presents a novel tool that is a first step in supporting the trend towards sample miniaturization and at-home sample collection, and may be readily used in clinical and diagnostic settings. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页数:11
相关论文
共 30 条
[1]   The Relationship Between Fluticasone Furoate Systemic Exposure and Cortisol Suppression [J].
Allen, Ann .
CLINICAL PHARMACOKINETICS, 2013, 52 (10) :885-896
[2]   Development of an LC-MS/MS method for the determination of endogenous cortisol in hair using 13C3-labeled cortisol as surrogate analyte [J].
Binz, Tina M. ;
Braun, Ueli ;
Baumgartner, Markus R. ;
Kraemer, Thomas .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2016, 1033 :65-72
[3]   Measuring agreement in method comparison studies [J].
Bland, JM ;
Altman, DG .
STATISTICAL METHODS IN MEDICAL RESEARCH, 1999, 8 (02) :135-160
[4]  
Blicharz T.M., NAT BIOMED ENG
[5]   A surrogate analyte-based liquid chromatography-tandem mass spectrometry method for the determination of endogenous cyclic nucleotides in rat brain [J].
Chen, Jie ;
Tabatabaei, Ali ;
Zook, Doug ;
Wang, Yan ;
Danks, Anne ;
Stauber, Kathe .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2017, 146 :361-368
[6]   Simultaneous determination of hair cortisol, cortisone and DHEAS with liquid chromatography-electrospray ionization-tandem mass spectrometry in negative mode [J].
Chen, Zheng ;
Li, Jifeng ;
Zhang, Jing ;
Xing, Xue ;
Gao, Wei ;
Lu, Zuhong ;
Deng, Huihua .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 929 :187-194
[7]   Effects of cortisol on carbohydrate, lipid, and protein metabolism: Studies of acute cortisol withdrawal in adrenocortical failure [J].
Christiansen, Jens Juel ;
Djurhuus, Christian B. ;
Gravholt, Claus H. ;
Iversen, Per ;
Christiansen, Jens Sandahl ;
Schmitz, Ole ;
Weeke, Jorgen ;
Jorgensen, Jens Otto Lunde ;
Moller, Niels .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (09) :3553-3559
[8]   CORTISOL DECREASES BONE-FORMATION BY INHIBITING PERIOSTEAL CELL-PROLIFERATION [J].
CHYUN, YS ;
KREAM, BE ;
RAISZ, LG .
ENDOCRINOLOGY, 1984, 114 (02) :477-480
[9]   Evaluation of the Performance and Hematocrit Independence of the HemaPEN as a Volumetric Dried Blood Spot Collection Device [J].
Deprez, Sigrid ;
Paniagua-Gonzalez, Lucia ;
Velghe, Sofie ;
Stove, Christophe P. .
ANALYTICAL CHEMISTRY, 2019, 91 (22) :14467-14475
[10]  
EMA, 2011, GUIDELINE BIOANALYTI, V44, P1