2008•Pharmaceutical Journal of Chinese People's Liberation ArmyRequires access

Pharmacokinetics of Venlafaxine

Meng Jin

Open publisher page 0 citations

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.

About this research paper

What this paper is about

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.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available 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.

Key concepts: Chromatography, Chemistry, Pharmacokinetics, Venlafaxine, Cmax, High-performance liquid chromatography, Isopropyl alcohol, Maprotiline

Related papers

Back to paper searchBrowse research topicsOriginal source
Pharmacokinetics of Venlafaxine — Research Paper | ScholarLens