LC–MS/MS quantification of 7α-hydroxy-4-cholesten-3-one (C4) in rat and monkey plasma

• Published in: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Vol. 1064; pp. 49 - 55
• Main Authors: Kang, Lijuan, Connolly, Thomas M., Weng, Naidong, Jian, Wenying
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.10.2017
• Subjects: 7α-hydroxy-4-cholesten-3-one (C4); Animals; Bile acid synthesis; Biomarker; Biomarkers - blood; Cholestenones - blood; Chromatography, Liquid - methods; CYP7A1; Haplorhini; LC–MS/MS; Linear Models; Quantification; Rats; Reproducibility of Results; Sensitivity and Specificity; Tandem Mass Spectrometry - methods; Bile acid synthesis; Biomarker; Quantification; LC–MS/MS; 7α-hydroxy-4-cholesten-3-one (C4); CYP7A1
• ISSN: 1570-0232; 1873-376X
• DOI: 10.1016/j.jchromb.2017.09.006

•First reported LC–MS method for C4 quantification in plasma of preclinical species.•Fast, simple, and reliable method with small sample volume requirement.•A surrogate matrix approach was used for the endogenous analyte.•Non-specific binding and choice of surrogate matrix was comprehensively discussed.•Potential endogenous interferences were chromatographically separated from analyte. 7α-hydroxy-4-cholesten-3-one (C4) is an oxidative enzymatic product of cholesterol metabolism via cholesterol 7α-hydroxylase, an enzyme also known as cholesterol 7-alpha-monooxygenase or cytochrome P450 7A1 (CYP7A1). C4 is a stable intermediate in the rate limiting pathway of bile acid biosynthesis. Previous studies showed that plasma C4 levels correlated with CYP7A1 enzymatic activity and could serve as a biomarker for bile acid synthesis. Here we developed and qualified a simple and robust high-throughput method using liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) to quantify C4 in rat and monkey plasma. As C4 being an endogenous compound, this method used calibration standards in 50/50: acetonitrile/water (v/v). In order to mimic the incurred samples, quality control samples were prepared in the authentic plasma. Stable isotope labeled C4 (C4-d7) was used as the internal standard. The sample volume for analysis was 20μL and the sample preparation method was protein precipitation with acetonitrile. The average endogenous C4 concentrations, from 10 different lots of rat and monkey plasma, were 53.0±16.5ng/mL and 6.8±5.6ng/mL, respectively. Based on these observed endogenous C4 levels, the calibration curve ranges were established at 1–200ng/mL and 0.5–100ng/mL for rat assay and monkey assay, respectively. The method was qualified with acceptable accuracy, precision, linearity, and specificity. Matrix effect, recovery, and plasma stability of bench-top, freeze-thaw, and long-term frozen storage were also evaluated. The method has been successfully applied to pre-clinical studies.