Electrochemical Determination of Morphine in Urine Samples by Tailoring FeWO4/CPE Sensor

Biosensors (Basel). 2022 Oct 27;12(11):932. doi: 10.3390/bios12110932.

Abstract

Morphine (MORPH) is natural alkaloid and mainly used as a pain reliever. Its monitoring in human body fluids is crucial for modern medicine. In this paper, we have developed an electrochemical sensor for submicromolar detection of MORPH. The sensor is based on modified carbon paste electrode (CPE) by investigating the FexW1-xO4 ratio in iron tungstate (FeWO4), as well as the ratio of this material in CPE. For the first time, the effect of the iron-tungsten ratio in terms of achieving the best possible electrochemical characteristics for the detection of an important molecule for humans was examined. Morphological and electrochemical characteristics of materials were studied. The best results were obtained using Fe1W3 and 7.5% of modifier in CPE. For MORPH detection, square wave voltammetry (SWV) was optimized. Under the optimized conditions, Fe1W3@CPE resulted in limit of detection (LOD) of the method of 0.58 µM and limit of quantification (LOQ) of 1.94 µM. The linear operating range between 5 and 85 µM of MORPH in the Britton-Robinson buffer solution (BRBS) at pH 8 as supporting electrolyte was obtained. The Fe1W3@CPE sensor resulted in good selectivity and excellent repeatability with relative standard deviation (RSD) and was applied in real-world samples of human urine. Application for direct MORPH detection, without tedious sample pretreatment procedures, suggests that developed electrochemical sensor has appeared to be a suitable competitor for efficient, precise, and accurate monitoring of the MORPH in biological fluids.

Keywords: carbon paste electrode; electroanalysis; iron tungstate; morphine; real-world sample; square wave voltammetry.

MeSH terms

  • Carbon* / chemistry
  • Electrochemical Techniques* / methods
  • Electrodes
  • Humans
  • Iron
  • Morphine Derivatives

Substances

  • Carbon
  • Iron
  • Morphine Derivatives

Grants and funding

This work was supported by the Ministry of Education, Science and Technological Development of Republic of Serbia Contract number: 451-03-68/2022-14/200168, and EUREKA project E!13303 and bilateral cooperation Serbia–Croatia, project No 337-00-205/2019-09/03. The authors are grateful to Slađana Savić for the chromatographic analysis of the samples.