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Rapid determination of corticosterone in mouse plasma by ultra fast liquid chromatography‐tandem mass spectrometry
Authors:Yanhong Poh  Li Wu  Qi‐Gang Zhou  Bao‐Chang Cai
Affiliation:1. School of Applied Science, Temasek Polytechnic, Singapore;2. College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China;3. College of Pharmacy, Nanjing Medical University, Nanjing, China;4. Lerner Research Institute, Cleveland Clinic, Cleveland, USA
Abstract:Major depressive disorder is a severe, life‐threatening and highly prevalent psychiatric disorder. A high percentage of people suffering from depression are characterized by hyperactivity of the hypothalamic–pituitary–adrenal axis, resulting in plasma glucocorticoid (cortisol in human and corticosterone in rodent) elevations. Glucocorticoid is a critical molecule in the onset of pathology of depression. A simple, highly sensitive and specific method based on ultra‐fast liquid chromatography–tandem mass spectrometry method has been developed for the quantitation of corticosterone in mouse plasma for the first time, which provides technical support for the high‐throughput measurement for clinical determination of corticosterone in biological samples. Samples were spiked with methanol to precipitate the protein, and then chromatographed on an Agilent Zorbax Eclipse Plus C18 (100 × 2.1 mm,1.8 µm) column by linear gradient elution with methanol and 0.1% formic acid as the mobile phase within 5 min. The detection of corticosterone was performed on ultra‐fast liquid chromatography–triple quadrupole tandem mass spectrometry in the positive ion. The ions [M + H]+ m/z 347.2 → m/z 311.1 for corticosterone and [M + H]+ m/z 363.2 → m/z 327.2 for hydrocortisone (internal standard) were used for quantitative determination. The lower quantification limit for corticosterone was 1 ng/mL. The validated method was successfully applied to the quantitation of corticosterone in mouse plasma. Copyright © 2014 John Wiley & Sons, Ltd.
Keywords:corticosterone  MDD  plasma  quantitative determination  UFLC‐MS/MS
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