Add time:08/06/2019         Source:sciencedirect.com

Simultaneous HPLC determination of the analgetic agent tramadol, its major pharmacodynamically active metabolite (O-desmethyltramadol) in human plasma is described. Simple methods for the preparation of the standard of the above-mentioned tramadol metabolite and N1,N1-dimethylsulfanilamide (used as the internal standard) are also presented. The analytical procedure involved a simple liquid–liquid extraction of the analytes from the plasma under the conditions described previously. HPLC analysis was performed on a 250×4 mm chromatographic column with LiChrospher 60 RP-selectB 5-μm (Merck) and consists of an analytical period where the mobile phase acetonitrile–0.01 M phosphate buffer, pH 2.8 (3:7, v/v) was used, and of a subsequent wash-out period where the plasmatic ballast compounds were eluted from the column using acetonitrile–ultra-high-quality water (8:2, v/v). The whole analysis, including the equilibration preceding the initial analytical conditions lasted 19 min. Fluorescence detection (λex 202 nm/λem 296 nm for tramadol and its metabolite, λex 264 nm/λem 344 nm for N1,N1-dimethylsulfanilamide) was used. The validated analytical method was applied to pharmacokinetic studies of tramadol in human volunteers.

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