| Literature DB >> 27643859 |
Xi Chen1, Bei Xu1, Jian Yang2, Juan Liu3, Dailong Fang1, Yongjun Gu1, Zhifei Jian1, Minghai Tang1, Chunmei Fu3, Zhi Zhang1, Chunling Jiang1, Xiangrong Song4.
Abstract
To investigate the pharmacokinetic (PK) interaction between telmisartan (Tel) and pitavastatin (Pit), a rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometric assay method had been successfully established and fully validated for the simultaneous quantification of Tel and Pit in rat plasma. A simple protein precipitation procedure was adopted for the sample preparation with satisfactory extraction recovery for both analytes and the internal standard. The samples were chromatographed on an Inertsil ODS-3 C18 column (100mm×2.1mm, 2μm) using a mixture of acetonitrile and 10mM ammonium acetate containing 0.1% formic acid (60: 40, v/v) as the mobile phase at a flow rate of 0.4mL/min. The calibration curves obtained were linear (r>0.99) over the concentration range of 2-200ng/mL for Tel and 1-100ng/mL for Pit, respectively. The validated method was successfully applied to the PK study and the data did not reveal any evidence for the potential drug-drug interaction (DDI) between Tel and Pit. This information would provide the evidence for clinical rational use of Tel and Pit, and this study might be applied in therapeutic drug monitoring in patients receiving Tel/Pit combinations or single drug.Entities:
Keywords: Drug interaction; LC–MS/MS; Pharmacokinetics; Pitavastatin; Telmisartan
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Year: 2016 PMID: 27643859 DOI: 10.1016/j.jpba.2016.09.006
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935