Rapid solid-phase extraction coupled with GC-MS method for the determination of venlafaxine in rat plasma: Application to the drug-drug pharmacokinetic interaction study of venlafaxine combined with fluoxetine.
Lin SongZhen ZhengChen LiangXiujuan ChenRunsheng ZhangZhanying HongYifeng ChaiPublished in: Journal of separation science (2017)
A rapid and sensitive gas chromatography with mass spectrometry method for the determination of venlafaxine in rat plasma has been developed and applied to a drug-drug interaction study of fluoxetine on pharmacokinetics of venlafaxine in rats. Rat plasma was spiked with 2% aqueous ammonia before subjected to preactivated C18 solid-phase extraction columns and eluted with methanol. No endogenous interferences were observed under optimal condition. The calibration curve was linear (R2 = 0.9994) in the range of 10-1000 ng/mL. The quantification limit of venlafaxine in rat plasma was 10 ng/mL. The accuracy was in the range of 85-110%, and the extraction recovery was no less than 50%. Both the intra- and interday precision were 5.0-10.7%. The concentration-time curve showed that plasma concentrations of the coadministration group (group B) were higher than that of single dose group (group A). Both values of Cmax (0.069 mg/L) and AUC0→∞ (0.291 mg h/L) in group B were statistically greater than that of Cmax (0.046 mg/L) and AUC0→∞ (0.181 mg·h/L) in group A (P < 0.05). The results indicated that a significant effect of fluoxetine was shown on the pharmacokinetics of venlafaxine, suggesting that drug-drug interactions are of concern for the treatment of depression with the combined use of venlafaxine and fluoxetine.
Keyphrases
- solid phase extraction
- gas chromatography
- liquid chromatography
- high performance liquid chromatography
- tandem mass spectrometry
- molecularly imprinted
- mass spectrometry
- liquid chromatography tandem mass spectrometry
- gas chromatography mass spectrometry
- simultaneous determination
- ultra high performance liquid chromatography
- high resolution mass spectrometry
- adverse drug
- drug induced
- high resolution
- capillary electrophoresis
- room temperature
- smoking cessation