Abstract

Pharmacologically active compounds are often detected in wastewater and surface waters. The nonsteroidal anti-inflammatory drug diclofenac (DCF) was included in the European watch list of substances that requires its environmental monitoring in the member states. DCF may harmfully influence the ecosystem already at concentrations ≤ 1 μg L−1. The fast and easy quantification of DCF is becoming a subject of global importance. Fluorescence polarization immunoassay (FPIA) is a homogeneous mix-and-read method which does not require the immobilization of reagents. FPIA can be performed in one phase within 20–30 min, making it possible to analyse wastewater without any complicated pre-treatment. In this study, new tracer molecules with different structures, linking fluorophores to derivatives of the analyte, were synthesized, three homologous tracers based on DCF, two including a C6 spacer, and one heterologous tracer derived from 5-hydroxy-DCF. The tracer molecules were thoroughly assessed for performance. Regarding sensitivity of the FPIA, the lowest limit of detection reached was 2.0 μg L−1 with a working range up to 870 μg L−1. The method was validated for real wastewater samples against LC-MS/MS as reference method with good agreement of both methods.Graphical abstract

Highlights

  • Diclofenac (DCF) is a nonsteroidal anti-inflammatory drug (NSAID) with analgesic, anti-inflammatory, and antipyretic properties

  • Mass spectrometric detection was performed on an Fluorescence polarization immunoassay for the determination of diclofenac in wastewater

  • The combination of tracer and antibody has a significant influence on sensitivity, selectivity, and reliability of an fluorescence polarization immunoassay (FPIA), and should always be carefully studied

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Summary

Introduction

Diclofenac (DCF) is a nonsteroidal anti-inflammatory drug (NSAID) with analgesic, anti-inflammatory, and antipyretic properties. The mechanism of action of diclofenac, like that of other NSAIDs, involves inhibition of cyclooxygenase (COX-1 and COX-2). Another pharmacological effect is the inhibition of prostaglandin synthesis in vitro [1]. Various instrumental methods have been applied for detection of DCF, including ultra-performance liquid chromatography (UPLC) coupled to high-resolution mass spectrometers [4, 5]. These techniques are expensive and require extensive sample preparation [6]

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