Abstract
This present study aims to develop a liquid chromatography coupled to tandem mass spectrometry assay to quantify phillyrin in rat plasma and tissues. Plasma and tissue samples were processed via protein precipitation, and calceolarioside B was chosen as the internal standard. Selected reactions monitoring mode was applied to detect the analytes of all samples. Mass spectrometry was conducted in the negative ion mode for detection. The MS/MS ion transitions monitored were m/z 533.4 → 370.8 for phillyrin and m/z 477.3 → 161.0 for calceolarioside B, respectively. All calibration curves were linear over the range of 1–800 ng/ml in each biological matrix. The lower limit of quantification for plasma and tissue homogenates was 1 ng/ml. Inter- and intra-day precision and accuracy well met within the acceptable ranges (≤ 15%). It was successfully applied to the pharmacokinetic and tissue distribution studies of phillyrin after intravenous doses of 0.1 mg/kg in rats.
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HW wrote the manuscript. SY carried out the data analyses. QX designed the study and supervised the laboratory work. All authors read the manuscript and approved the submission.
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Wang, H., Yang, S. & Xian, Q. Pharmacokinetics and Tissue Distribution of Phillyrin in Rats. Rev. Bras. Farmacogn. 30, 818–823 (2020). https://doi.org/10.1007/s43450-020-00100-x
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DOI: https://doi.org/10.1007/s43450-020-00100-x