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OBJECTIVE: To develop a quick, sensitive and accurate high performance liquid chromatography tandem mass spectrometric(HPLC-MS/MS) method for quantification of VND3207 and its metabolites in rat plasma and to investigate pharmacokinetics of VND3207 in SD rats. METHODS: Rats were ig given VND3207 70 mg·kg-1. Blood samples were collected and separated by liquid chromatography on a C18 reversion phase chromatographic column with gradient elution. Concentration of VND3207 and its metabolites syringic acid and syringic alcohol were detected by HPLC-MS/MS in positive multiple reaction monitoring mode. Pharmacokinetic parameters of VND3207 and its metabolites were calculated. RESULTS: Calibration curves of VND3207 and its metabolites syringic acid and syringic alcohol were linear within the range of 2-2000 μg·L -1, ranged from quantification limit 2 μg·L-1. Intra- and inter-day precision was both less than 15%, and accuracy with 91.2%-110.7%. The concentrations of VND3207 and its metabolites were detected in plasma of rats up to 12 h after VND3207 was ig given to rats. AUC 0-∞ of VND3207, syringic acid and syringic alcohol were 19.37 ± 10.56, 1825.32 ± 719.97 and (9.89 ± 1.75) mg·L-1·min, and T1/2 was 78.0 ± 44.6, 114.4 ± 17.9 and (66.0 ± 23.8) min, respectively. CONCLUSION: A quick, sensitive and accurate HPLC-MS/MS method is developed for quantification of VND3207 and its metabolites in rat plasma. VND3207 is absorbed and metabolized rapidly. A large amount of VND3207 is oxidized to syringic acid while a small amount is reduced to syringic alcohol.
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