Abstract

Application of the poly-ɛ-caprolactone composite sorbent consisting of the micro- and nanometer fibers for the on-line extraction of non-steroidal anti-inflammatory drugs from a biological matrix has been introduced. A 100 μL human serum sample spiked with ketoprofen, naproxen, sodium diclofenac, and indomethacin was directly injected in the extraction cartridge filled with the poly-ɛ-caprolactone composite sorbent. This cartridge was coupled with a chromatographic instrument via a six-port switching valve allowing the analyte extraction and separation within a single analytical run. The 1.5 min long extraction step isolated the analytes from the proteinaceous matrix was followed by their 13 min HPLC separation using Ascentis Express RP-Amide (100 × 4.6 mm, 5 µm) column. The recovery of all analytes from human serum tested at three concentration levels ranged from 70.1% to 118.7%. The matrix calibrations were carried out in the range 50 to 20,000 ng mL−1 with correlation coefficients exceeding 0.996. The detection limit was 15 ng mL−1, and the limit of quantification corresponded to 50 ng mL−1. The developed method was validated and successfully applied for the sodium diclofenac determination in real patient serum. Our study confirmed the ability of the poly-ɛ-caprolactone composite sorbent to remove the proteins from the biological matrix, thus serving as an alternative to the application of restricted-access media.

Highlights

  • Non-steroidal anti-inflammatory drugs (NSAID) are widely used in pain, osteoarthritis, and rheumatoid arthritis treatment

  • Numerous methods for NSAID determination in biological fluids including gas chromatography [4,5,6], capillary electrophoresis [7,8,9], and liquid chromatography [10,11] were developed over the past years

  • The NSAID are usually determined in plasma, where the direct analysis of untreated matrix can lead to lower sensitivity, unprecise results, and in the worst case to irreversible damage of the chromatography column caused by protein precipitation

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Summary

Introduction

Non-steroidal anti-inflammatory drugs (NSAID) are widely used in pain, osteoarthritis, and rheumatoid arthritis treatment. A mechanism of their action lies in the inhibition of cyclo-oxygenase enzyme, an enzyme serving prostaglandin biosynthesis. These drugs play a crucial role in the suppression of the inflammatory response of an organism. The reduction in prostaglandin levels results in antipyretics, analgesics, and anti-inflammatory activity of NSAID. Monitoring of NSAID in body fluid is essential for toxicological and pharmacokinetics studies. Their determination as a part of rational pharmacotherapy that aims to reduce risks and achieve disease treatment goals is less common

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