Abstract

In this work an application of optical fiber sensors for real-time optical monitoring of electrochemical deposition of ketoprofen during its anodic oxidation is discussed. The sensors were fabricated by reactive magnetron sputtering of indium tin oxide (ITO) on a 2.5 cm-long core of polymer-clad silica fibers. ITO tuned in optical properties and thickness allows for achieving a lossy-mode resonance (LMR) phenomenon and it can be simultaneously applied as an electrode in an electrochemical setup. The ITO-LMR electrode allows for optical monitoring of changes occurring at the electrode during electrochemical processing. The studies have shown that the ITO-LMR sensor’s spectral response strongly depends on electrochemical modification of its surface by ketoprofen. The effect can be applied for real-time detection of ketoprofen. The obtained sensitivities reached over 1400 nm/M (nm·mg−1·L) and 16,400 a.u./M (a.u.·mg−1·L) for resonance wavelength and transmission shifts, respectively. The proposed method is a valuable alternative for the analysis of ketoprofen within the concentration range of 0.25–250 μg mL−1, and allows for its determination at therapeutic and toxic levels. The proposed novel sensing approach provides a promising strategy for both optical and electrochemical detection of electrochemical modifications of ITO or its surface by various compounds.

Highlights

  • Demand for nonprescription drugs, such as 2-(3-benzoylphenyl)-propanoic acidis expected to increase in the near future

  • This part of the experiment was done in order to estimate the sensitivity of the device to changes of optical properties at the indium tin oxide (ITO)

  • The probes were installed in a setup allowing one to record the transmission spectra, while the sensor was consecutively immersed in different refractive index (RI) solutions

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Summary

Introduction

Demand for nonprescription drugs, such as 2-(3-benzoylphenyl)-propanoic acid (ketoprofen, KP)is expected to increase in the near future. Several methods have already been reported for quantitative determination of KP, including liquid chromatography-mass spectrometry [3], UV-fluorescence [4], ion chromatography [5], flow injection with chemiluminescence [6], or electrochemical detection [7] Both chromatographic and non-chromatographic techniques usually require rigorous sample preparation and expensive extraction methods (including solid-phase extraction) when real samples are considered. Mass spectrometry in turn requires analyte signal suppression or enhancement during electrospray ionization, especially for analysis of multi-compound samples. Application of all these methods is time-consuming and requires expensive and highly specialized setups which are only available in well-equipped research laboratories. Photometric UV and fluorescence-based methods commonly suffer from low sensitivity and selectivity, while the latter require specific chemicals or compounds (e.g., nanoparticles) in the detection procedure

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