Journal
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES
Volume 30, Issue 3, Pages 393-403Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/10826070601084860
Keywords
capillary liquid chromatography; column switching; oxomemazine; liquid-liquid extraction; mass spectrometry
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A method based on on-line solid phased extraction capillary liquid chromatography-electrospray ionization-mass spectrometry (SPE-capLC-ESI-MS) has been developed for the determination of oxomemazine in human plasma. Prior to injection, 0.5 mL of plasma spiked with metronidazole (internal standard) was mixed with ammonium formate buffer and methyl orange, which served as an ion pair reagent for effective chloroform liquid - liquid extraction. The employment of methyl orange as an ion pair reagent doubled the extraction efficiency, as compared to not using methyl orange. In preliminary experiments, conventional LC-UV instrumentation was employed. However, it was found that employing a capillary column with an inner diameter of 0.3 mm increased the sensitivity by a factor of similar to 100, when injecting the same mass of analyte. Incorporating an easily automated reversed phase column switching system with SPE made it possible to inject up to 100 mL of solution, and the total analysis time was 5 minutes. The method was validated in the range 3 to 30 ng/mL oxomemazine, yielding a correlation coefficient of 0.99 (r(2)). The within-assay and between-assay precisions were between 6.7 and 12% and 6.8 and 7.4%, respectively. The method was used to determine the amount of oxomemazine in a healthy female 20 hours after an lintake of 1 teaspoon (approximately 1 mL) of the cough syrup Toplexil (R), which contains 0.033 g oxomemazine per 100 mL syrup. Oxomemazine was detected, and the concentration was calculated to 2.0 ng/mL plasma.
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