<p>Analysis of critical biomarkers like <span>l</span>-lactate is extremely important in clinical practice. Herein, a non-invasive and sensitive colorimetric biosensor for accurate <span>l</span>-lactate determination has been developed. The proposed method demonstrates the ability of Fe<sup>3+</sup> ions of iron(III) chloride to substitute the traditional horseradish peroxidase enzyme in the colorimetric determination of <span>l</span>-Lactate. The biosensor is based on the release of H<sub>2</sub>O<sub>2</sub> by lactate oxidase enzyme (LOx) after 30&#xa0;min incubation in a 37&#xa0;°C water bath. Subsequently, H<sub>2</sub>O<sub>2</sub> reacts with 3,3′,5,5′-tetramethylbenzidine substrate (TMB) catalyzed by Fe<sup>3+</sup> ion utilizing its peroxidase-mimetic activity. Fe<sup>3+</sup> ion has peroxidase-like activity which could rapidly catalyze the oxidation reaction of TMB by H<sub>2</sub>O<sub>2,</sub> producing a characteristic blue colored product at 30&#xa0;°C water bath for 15&#xa0;min. Based on the catalytic mechanism of fast electron transfer between TMB and H<sub>2</sub>O<sub>2</sub> with the assistance of the intrinsic peroxidase-like activity of Fe<sup>3+</sup> ion, a colorimetric biosensor for determination of <span>l</span>-lactate was developed. The obtained colored product of oxidized TMB could be measured spectrophotometrically at λmax 652&#xa0;nm. The biosensor yielded a reproducible response over a linear range of 5 µM–20 µM of <span>l</span>-lactate with a limit of detection of 1.278 µM. Furthermore, satisfactory results were obtained upon application of the method to artificial saliva samples.</p>

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Development of a biosensor for spectrophotometric determination of l-lactate in artificial saliva

  • Rehab E. Bayoumy,
  • Nariman A. El-Ragehy,
  • Nagiba Y. Hassan,
  • Amr M. Mahmoud

摘要

Analysis of critical biomarkers like l-lactate is extremely important in clinical practice. Herein, a non-invasive and sensitive colorimetric biosensor for accurate l-lactate determination has been developed. The proposed method demonstrates the ability of Fe3+ ions of iron(III) chloride to substitute the traditional horseradish peroxidase enzyme in the colorimetric determination of l-Lactate. The biosensor is based on the release of H2O2 by lactate oxidase enzyme (LOx) after 30 min incubation in a 37 °C water bath. Subsequently, H2O2 reacts with 3,3′,5,5′-tetramethylbenzidine substrate (TMB) catalyzed by Fe3+ ion utilizing its peroxidase-mimetic activity. Fe3+ ion has peroxidase-like activity which could rapidly catalyze the oxidation reaction of TMB by H2O2, producing a characteristic blue colored product at 30 °C water bath for 15 min. Based on the catalytic mechanism of fast electron transfer between TMB and H2O2 with the assistance of the intrinsic peroxidase-like activity of Fe3+ ion, a colorimetric biosensor for determination of l-lactate was developed. The obtained colored product of oxidized TMB could be measured spectrophotometrically at λmax 652 nm. The biosensor yielded a reproducible response over a linear range of 5 µM–20 µM of l-lactate with a limit of detection of 1.278 µM. Furthermore, satisfactory results were obtained upon application of the method to artificial saliva samples.