The pharmacokinetics of zopicolone tablet in 10 healthy male volunteers
Yuan Hai
Abstract
Yuan Hai
Abstract
OBJECTIVE To study the pharmacokinetics of zopicolone in 10 healthy male volunteers.METHODS The blood samples were obtained at 0,0.25,0.75 1.0,1.5,2.0,3.0,4.0,6.0,8.0,12,24 h after a single dose administration of 15 mg zopicolone tablet.The plasma zopicolone concentration was determined by HPLC.The pharmacokinetics of zopicolone were analysed by 3P87 program.RESULTS The main pharmacokinetic paramerers of zopicolone were K a (11.03±10.38) h -1 ,AUC 0~24 (1 049.61±286.02) ng·h·mL -1 , c max (109.35±30.89) ng·mL -1 , t max (1.32±1.24) h and t 1/2(Ke) (5.97±1.49) h,respectively.CONCLUSIONS Zopicolone could be absorbed rapidly and its pharmacokinetics was consistent with one compartment model.
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OBJECTIVE To study the pharmacokinetics of zopicolone in 10 healthy male volunteers.METHODS The blood samples were obtained at 0,0.25,0.75 1.0,1.5,2.0,3.0,4.0,6.0,8.0,12,24 h after a single dose administration of 15 mg zopicolone tablet.The plasma zopicolone concentration was determined by HPLC.The pharmacokinetics of zopicolone were analysed by 3P87 program.RESULTS The main pharmacokinetic paramerers of zopicolone were K a (11.03±10.38) h -1 ,AUC 0~24 (1 049.61±286.02) ng·h·mL -1 , c max (109.35±30.89) ng·mL -1 , t max (1.32±1.24) h and t 1/2(Ke) (5.97±1.49) h,respectively.CONCLUSIONS Zopicolone could be absorbed rapidly and its pharmacokinetics was consistent with one compartment model.
Key concepts: Pharmacokinetics, Pharmacology, High-performance liquid chromatography, Plasma concentration, Chemistry, Blood concentration, Medicine, Chromatography