Synthesis and Characterization of a Novel Modified Biosensor Carbon/Chitosan L-Leucine and Albumin Electrode for Bilirubin and Uric Acid Blood Detection

Bilirubin (BR) is a yellow-to-orange bile pigment produced by hemoglobin breakdown. It circulates in the blood, is absorbed by the liver, and then conjugated to form bilirubin diglucuronide. Its increased level in serum (Hyperbilirubinemia) may considered as an indication of certain diseases such as neonatal jaundice, hepatitis, and severe liver failure with cirrhosis. Thus, the monitoring of BR in plasma is clinically important. Herein, a novel carbon/chitosan paste electrode modified by L-leucine and Albumin (C/Chi-PL-BSA) is synthesized and tested for electrochemical sensitive determination of BR and Uric Acid. Significate sensitivity and important selectivity in the linear range of 1.00–150.00 μM for BR, and 10.00–600.00 μM for UA were obtained. Moreover, micromolar detection limits of 0.40 μM for BR and 1.00 μM for UA were achieved at pH13. The proposed oxidation mechanisms of BR and UA in alkaline media have been supported by DFT calculations at the B3LYP/ 6–31 G(d) level of theory. The easy preparation and high reproducibility made this electrode very appropriate in pharmaceutical preparations for the electrochemical determination of BR. Furthermore, Analyses using human serum were performed, demonstrating a high percentage of recovery.

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Publication Details

Journal
Journal of The Electrochemical Society
Published
2024-09-02
DOI
https://doi.org/10.1149/1945-7111/ad7989
Citations
2
Primary Topic
Electrochemical sensors and biosensors
Type
article
Field-Weighted Citation Impact
0.42

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article

Synthesis and Characterization of a Novel Modified Biosensor Carbon/Chitosan L-Leucine and Albumin Electrode for Bilirubin and Uric Acid Blood Detection

Khalid Riffi Temsamani, Mohammed Lamarti Sefian, El Hassane Anouar, Wafaa S. Abo El‐Yazeed et al.
2 citations
Journal of The Electrochemical Society
Electrochemical sensors and biosensors
0.42
article

Synthesis and Characterization of a Novel Modified Biosensor Carbon/Chitosan L-Leucine and Albumin Electrode for Bilirubin and Uric Acid Blood Detection

Khalid Riffi Temsamani, Mohammed Lamarti Sefian, El Hassane Anouar, Wafaa S. Abo El‐Yazeed, Redouan El Khamlichi, Hanan A. Albalwi, Dounia Bouchta, Jalal Kassout, Said Boudra, Lamia-e Khamlichi
article en
2 citations

Abstract

Bilirubin (BR) is a yellow-to-orange bile pigment produced by hemoglobin breakdown. It circulates in the blood, is absorbed by the liver, and then conjugated to form bilirubin diglucuronide. Its increased level in serum (Hyperbilirubinemia) may considered as an indication of certain diseases such as neonatal jaundice, hepatitis, and severe liver failure with cirrhosis. Thus, the monitoring of BR in plasma is clinically important. Herein, a novel carbon/chitosan paste electrode modified by L-leucine and Albumin (C/Chi-PL-BSA) is synthesized and tested for electrochemical sensitive determination of BR and Uric Acid. Significate sensitivity and important selectivity in the linear range of 1.00–150.00 μM for BR, and 10.00–600.00 μM for UA were obtained. Moreover, micromolar detection limits of 0.40 μM for BR and 1.00 μM for UA were achieved at pH13. The proposed oxidation mechanisms of BR and UA in alkaline media have been supported by DFT calculations at the B3LYP/ 6–31 G(d) level of theory. The easy preparation and high reproducibility made this electrode very appropriate in pharmaceutical preparations for the electrochemical determination of BR. Furthermore, Analyses using human serum were performed, demonstrating a high percentage of recovery.

Journal of The Electrochemical SocietyVol. 171(9)
Prince Sattam bin Abdulaziz University
Openalex Percentile: Top 38%
Electrochemical sensors and biosensors
0.42
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Synthesis and Characterization of a Novel Modified Biosensor Carbon/Chitosan L-Leucine and Albumin Electrode for Bilirubin and Uric Acid Blood Detection — Khalid Riffi Temsamani, Mohammed Lamarti Sefian, et al. · Journal of The Electrochemical Society (2024) | TGRS Research Map | TGRS