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Direct analysis of indomethacin in rat plasma using a column-switching high-performance liquid chromatographic system. | LitMetric

Direct analysis of indomethacin in rat plasma using a column-switching high-performance liquid chromatographic system.

J Chromatogr B Analyt Technol Biomed Life Sci

Research Department, Saitama Daiichi Pharmaceutical, Ltd, Kasukabe, Saitama, Japan.

Published: February 2002

AI Article Synopsis

  • A fully automated analytical method was developed for determining indomethacin levels in rat plasma using a high-performance chromatographic system that includes a precolumn and an analytical column.
  • The method involves enriching the drug in the precolumn through on-line solid-phase extraction followed by elution and separation on the analytical column, utilizing specific mobile phase and detection conditions.
  • The assay demonstrates high sensitivity, accuracy, and linearity for indomethacin, making it effective for studying the pharmacokinetics of topical indomethacin administration in rats across various pharmaceutical studies.

Article Abstract

We have established a robust, fully automated analytical method for the determination of indomethacin in rat plasma using a column-switching high-performance chromatographic system. The system consists of a precolumn and an analytical column connected in series via a switching valve. When a 50-microl portion of rat plasma containing a therapeutic level of indomethacin was applied directly to the system, the drug was automatically enriched in the precolumn (TSK BSA-ODS) by on-line solid-phase extraction. After elution of the plasma proteins, the analyte was automatically transferred to the analytical column (Zorbax Eclipse XDBC18) where chromatography was performed using isocratic elution and UV absorption detection at a wavelength of 254 nm. The separation mobile phase consisted of methanol-0.1% phosphoric acid (70:30, v/v) at a flow-rate of 1 ml/min. The calibration line for indomethacin showed good linearity in the range 50-10 000 ng/ml (r>0.999) with the detection quantification of 50 ng/ml (RSD=2.6%). Accuracy ranged from -0.62 to 3.22%, and the within- and between-day precision of the assay was better than 6% across the calibration range. The analytical sensitivity and accuracy of this assay is suitable for characterization of the pharmacokinetics of topical administration of imdomethacin to rats. The method has been successfully used to provide pharmacokinetic data in a large number of diverse pharmaceutical studies.

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Source
http://dx.doi.org/10.1016/s0378-4347(01)00532-1DOI Listing

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