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Drug Dependence Research Center, Department of Psychiatry, University of California, San Francisco, San Francisco, CA 94143.
a Address correspondence to this author at: Langley Porter Psychiatric Institute, Box CPR0984, University of California, San Francisco, 401 Parnassus Ave., San Francisco, CA 94143-0984. Fax 415-476-7690.
We describe a sensitive and specific method for the measurement of buprenorphine in human plasma. The method involves a structural analog as an internal calibrator, careful control of pH during sample extraction to maximize drug recovery, and back-extraction into acid followed by reextraction to eliminate endogenous interferences. After evaporation, sample residues are derivatized with heptafluorobutyric anhydride and analyzed by separation on a fused-silica polymethylsiloxane capillary column and electron-capture detection. Calibration curves were linear in the ranges 0.12.0 µg/L and 2.020 µg/L, with within-run CVs of 9.7% at 0.1 µg/L to 5.0% at 20 µg/L, and total CVs of 15.9% at 0.1 µg/L to 6.5% at 10 µg/L. The limit of quantification was 0.1 µg/L. The method was utilized in studies to determine the absolute bioavailability of sublingual doses of 2 mg of buprenorphine in 1 mL of 300 mL/L ethanol and the bioequivalence of sublingual 8-mg tablet and 300 mL/L ethanol solution formulations.
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D. A. Ciraulo, R. J. Hitzemann, E. Somoza, C. M. Knapp, J. Rotrosen, O. Sarid-Segal, A. M. Ciraulo, D. J. Greenblatt, and C. N. Chiang Pharmacokinetics and Pharmacodynamics of Multiple Sublingual Buprenorphine Tablets in Dose-Escalation Trials J. Clin. Pharmacol., February 1, 2006; 46(2): 179 - 192. [Abstract] [Full Text] [PDF] |
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