Abstract
Currently, there are no FDA approved medications for treatment of cocaine addiction underscoring the dire need to develop such a product. There is an accumulating body of evidence that l-tetrahydropalmatine (l-THP), a non-selective dopamine antagonist, can be used for the treatment of cocaine addiction. Indeed, the FDA recently approved its usage in a Phase I study in cocaine abusers and it was indispensable to develop a simple and sensitive method for the simultaneous determination of l-THP and cocaine in human plasma. We developed a UPLC-FLD method for quantitation of these molecules using an ACQUITY BEH C18 column (2.1. mm. ×. 50. mm, 1.7. μm) and a mobile phase that consisted of 10. mM ammonium phosphate (pH = 4.75), methanol, and acetonitrile (v:v:v, 78:16:6). Venlafaxine was used as the internal standard while hexane was used for the liquid-liquid extraction. The flow rate was 0.4. mL/min with fluorescence detection using an excitation wavelength of 230. nm and emission detection wavelength of 315. nm. This method was selective, linear and sensitive with a lower limit of quantification of 2.5. ng/mL for both cocaine and l-THP. The intra-day precision of cocaine and l-THP was <9.50% while the accuracy was <4.29%. The inter-day precision of cocaine and l-THP was <9.14%, and the accuracy was <12.49%. The recovery for cocaine and l-THP ranged from 43.95 to 50.02% and 54.65 to 58.31%, respectively. In comparison to forty reported cocaine quantitation methods this method is simple, sensitive and cost-effective and can be used for simultaneous quantitation of l-THP and cocaine. This method meets the FDA guidelines and can be used in current and future clinical studies. © 2014.
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Yu, M., Hassan, H. E., Ibrahim, A., Bauer, K. S., Kelly, D. L., & Wang, J. B. (2014). Simultaneous determination of l-tetrahydropalmatine and cocaine in human plasma by simple UPLC-FLD method: Application in clinical studies. Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, 965, 39–44. https://doi.org/10.1016/j.jchromb.2014.06.020
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