Pharmacokinetics of Venlafaxine
Meng Jin
Abstract
Meng Jin
Abstract
Aim To establish a method to determine the concentration of venlafaxine in human plasma using High performance Liquid Chromatography-Fluoresence (HPLC-F). Methods The analytical column was Diamonsil C18(150mm×4.6mm,5 μm);the mobile phase was acetonitrile-phosphate buffer solution(pH 3.0)-triethylamine(33.5∶ 66.5∶ 1,V/V/V);the flow rate was 1.0ml/min;and the injection volume was 20 μl,and the internal standard was maprotiline. Plasma samples were extracted with n-hexane and isopropyl alcohol with fluorimetric detection (λex 276 nm, λem 596 nm). Results The linear range of venlafaxine in human plasma was 10~800ng · ml-1(r=0.999 9). The lowest detectable plasma concentration was 16.99ng · ml-1(S/N3). The extraction and relative recoveries of venlafaxine over plasma concentration 30,150,600ng · ml-1 were 81.51%~91.08% and 98.7 %~112.6 % respectively. The RSD of within-day and between-day were less than12% and 10%(n=5), respectively. The parameters:t1/2(6.57±2.81)h,Tmax(3.11±0.93)h,Cmax(273.38±75.44)ng · ml-1, AUC(0~t)(2 237.54±816.67)ng · h · ml-1,AUC(0~∞)(2 456.13±838.30)ng · h · ml-1.Conclusion The method is proved to be convenient,specific,sensitive enough to be applied to pharmacokinetic studies of venlafaxine in human plasma.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Aim To establish a method to determine the concentration of venlafaxine in human plasma using High performance Liquid Chromatography-Fluoresence (HPLC-F). Methods The analytical column was Diamonsil C18(150mm×4.6mm,5 μm);the mobile phase was acetonitrile-phosphate buffer solution(pH 3.0)-triethylamine(33.5∶ 66.5∶ 1,V/V/V);the flow rate was 1.0ml/min;and the injection volume was 20 μl,and the internal standard was maprotiline. Plasma samples were extracted with n-hexane and isopropyl alcohol with fluorimetric detection (λex 276 nm, λem 596 nm). Results The linear range of venlafaxine in human plasma was 10~800ng · ml-1(r=0.999 9). The lowest detectable plasma concentration was 16.99ng · ml-1(S/N3). The extraction and relative recoveries of venlafaxine over plasma concentration 30,150,600ng · ml-1 were 81.51%~91.08% and 98.7 %~112.6 % respectively. The RSD of within-day and between-day were less than12% and 10%(n=5), respectively. The parameters:t1/2(6.57±2.81)h,Tmax(3.11±0.93)h,Cmax(273.38±75.44)ng · ml-1, AUC(0~t)(2 237.54±816.67)ng · h · ml-1,AUC(0~∞)(2 456.13±838.30)ng · h · ml-1.Conclusion The method is proved to be convenient,specific,sensitive enough to be applied to pharmacokinetic studies of venlafaxine in human plasma.
Key concepts: Chromatography, Chemistry, Pharmacokinetics, Venlafaxine, Cmax, High-performance liquid chromatography, Isopropyl alcohol, Maprotiline