Abstract
A new LC method has been developed and validated for the direct determination of bupropion and its main metabolite, hydroxybupropion in human plasma. Plasma samples were analyzed after a simple, one step protein precipitation with trichloroacetic acid using a C8 column and mobile phase, consisting of methanol/acetonitrile/phosphate buffer (10 mM, pH 3.0) (40:10:50, v/v/v) and 20 mM 1-heptane sulfonic acid sodium salt with carbamazepine as the internal standard. UV detection was performed at 214 and 254 nm. The method was validated over the concentration range of 60–2,400 and 150–4,700 ng mL−1 for bupropion and hydroxybupropion, respectively. The intra- and inter-day assay variability was less than 15% for the two analytes. Limit of detection values were 24.8 and 63.4 ng mL−1 for bupropion and hydroxybupropion, respectively. The method developed was applied to quantification of bupropion and hydroxybupropion in human plasma.
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Acknowledgments
The authors appreciate the support of the Research Council of Anadolu University for our project (Project No. 060324) and GlaxoSmithKline (Istanbul, Turkey) for the gift sample of standard BUP and HBUP. D.Y. acknowledges a scholarship for Ph.D. students from the Scientific and Technical Research Council of Turkey (TUBITAK).
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Yeniceli, D., Dogrukol-Ak, D. An LC Method for the Determination of Bupropion and Its Main Metabolite, Hydroxybupropion in Human Plasma. Chroma 70, 1703–1708 (2009). https://doi.org/10.1365/s10337-009-1361-z
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DOI: https://doi.org/10.1365/s10337-009-1361-z