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摘要
The objective of the present study was to develop a selective and sensitive liquid chromatography-mass spectrometry (LC-MS) method for the simultaneous quantitation of capecitabine, 5'-deoxy-5-fluorocytidine (5'-DFCR), 5'-deoxy-5-fluorouridine (5'-DFUR), 5-fluorouracil (5-FU), and 5-fluorodihydrouracil (5-FUH2) in human plasma. Chromatography was performed on an Atlantis dC18 column with a mobile phase consisting of 1% formic acid in acetonitrile and 1% formic acid in water gradient elution. 5-fluorocytosine (5-FC) was used as internal standard. LC-MS data were acquired in SIM mode at m/z 130 for 5-FC, m/z 131 for 5-FU, m/z 133 for 5-FUH2, m/z 246 for 5'-DFCR, m/z 247 for 5'-DFUR, and m/z 360 for capecitabine. The drug/internal standard peak area ratios were linked via quadratic relationships to concentrations (100-10000g/L for 5-FU; 50-10000g/L for 5-FUH2; and 25-10000g/L for 5'-DFCR, 5'-DFUR, and capecitabine). The analysis of blank matrices from different donors showed the absence of interfering endogenous components at the retention times of the analytes. No evidence of matrix effect was observed. The method was precise (precision, 0.2-8.3%) and accurate (recovery, 99-104%). Mean extraction efficiencies 89% for each analyte were obtained. The lower limits of quantitation were 25g/L for capecitabine, 5'-DFCR, and 5'-DFUR; 50g/L for 5-FUH2; and 100g/L for 5-FU. This method was successfully used to investigate plasma concentrations of capecitabine and its metabolites in a pharmacokinetic study carried out in patients with metastatic solid tumors receiving oral administration of capecitabine (1600 to 3420mg according to the patient) twice a day.
- 出版日期2010
