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Development and validation of a solid-phase extraction-liquid chromatographic method for determination of amoxicillin in plasma.

N Lindegårdh·T Singtoroj·A Annerberg·N J White·N P J Day
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Abstract

A bioanalytic method for the determination of amoxicillin in plasma by hydrophilic interaction solid-phase extraction and liquid chromatography has been developed and validated. Plasma was precipitated with acetonitrile before samples were loaded onto a zwitterionic hydrophilic interaction liquid chromatography (ZIC-HILIC) solid-phase extraction column. Amoxicillin was analyzed by liquid chromatography on an Aquasil (150 x 4.6 mm) LC column with mobile-phase acetonitrile: phosphate buffer (pH 2.5; 0.1 mol/L) (7:93, v/v) and UV detection at 230 nm. A regression model using 1/concentration weighting was found the most appropriate for quantification. The intraassay precision for plasma was 3.3% at 15.0 microg/mL and 10.9% at 0.200 microg/mL. The interassay precision for plasma was 1.8% at 15.0 microg/mL and 7.5% at 0.200 microg/mL. The total-assay precision for plasma over 4 days using a total of 20 replicates was 13.2%, 5.5%, and 3.8% at 0.200 microg/mL, 3.00 microg/mL, and 15.0 microg/mL, respectively. The lower limit of quantification and the limit of detection were 0.050 microg/mL and 0.025 microg/mL, respectively, for 100 microL plasma. Long-term storage stability studies of amoxicillin in plasma indicate that a temperature of -80 degrees C is necessary to prevent degradation of amoxicillin.

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AmoxicillinCalibrationChromatography, LiquidDrug MonitoringDrug StabilityHumansReference StandardsReproducibility of ResultsJournal ArticleResearch Support, Non-U.S. Gov'tValidation Study

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N Lindegårdh, T Singtoroj, A Annerberg, N J White, N P J Day. 2005. Development and validation of a solid-phase extraction-liquid chromatographic method for determination of amoxicillin in plasma.. https://doi.org/10.1097/01.ftd.0000158082.38330.85

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