Development of an enzymatic biosensor to determine eugenol in dental samples

A GCE/CRGO-βCD′s/ADA-SPE/AuNPs biosensor was successfully developed to determine eugenol in dental samples. The optimal conditions to construct the biosensor were obtained from an experimental design based on the response surfaces methodology. The GCE/CRGO-βCD/ADA-SPE/AuNPs biosensor exhibited a ver...

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Published inTalanta (Oxford) Vol. 210; p. 120647
Main Authors Lopez, Jimena Claudia, Zon, María Alicia, Fernández, Héctor, Granero, Adrian Marcelo
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.04.2020
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Abstract A GCE/CRGO-βCD′s/ADA-SPE/AuNPs biosensor was successfully developed to determine eugenol in dental samples. The optimal conditions to construct the biosensor were obtained from an experimental design based on the response surfaces methodology. The GCE/CRGO-βCD/ADA-SPE/AuNPs biosensor exhibited a very good analytical performance for the quantification of eugenol. Thus, it shows a linear range between 1.3 × 10−8 and 1 × 10−5 mol L−1, with a sensitivity of (5.3 ± 0.3) x 10−3 A mol−1 L. The limits of detection and quantification were 4 × 10−9 mol L−1 and 1.3 × 10−8 mol L−1, respectively. Biosensors had an intraday and inter day reproducibility of 5% and 8%, respectively. The repeatability was of 3%, and the stability was 21 days (a decrease of 30% in current responses was observed after the fourth week). Recovery studies were performed in order to validate the proposed method. Recovery percentages were between 94 and 108%. A value of the apparent Michaellis-Menten constant, KMapp, of 3.1 × 10−6 mol L−1 was obtained using both Lineweaver-Burk and Eadi-Hofstee methods. [Display omitted] •An enzymatic biosensor to determine eugenol in dental samples is proposed.•Soybean peroxidase enzyme is used as the biological component.•Supramolecular chemistry is explored.•The working electrodes are modified glassy carbon electrodes.•Chemically reduced graphene oxide is used.
AbstractList A GCE/CRGO-βCD's/ADA-SPE/AuNPs biosensor was successfully developed to determine eugenol in dental samples. The optimal conditions to construct the biosensor were obtained from an experimental design based on the response surfaces methodology. The GCE/CRGO-βCD/ADA-SPE/AuNPs biosensor exhibited a very good analytical performance for the quantification of eugenol. Thus, it shows a linear range between 1.3 × 10 and 1 × 10  mol L , with a sensitivity of (5.3 ± 0.3) x 10  A mol  L. The limits of detection and quantification were 4 × 10  mol L and 1.3 × 10  mol L , respectively. Biosensors had an intraday and inter day reproducibility of 5% and 8%, respectively. The repeatability was of 3%, and the stability was 21 days (a decrease of 30% in current responses was observed after the fourth week). Recovery studies were performed in order to validate the proposed method. Recovery percentages were between 94 and 108%. A value of the apparent Michaellis-Menten constant, K , of 3.1 × 10  mol L was obtained using both Lineweaver-Burk and Eadi-Hofstee methods.
A GCE/CRGO-βCD′s/ADA-SPE/AuNPs biosensor was successfully developed to determine eugenol in dental samples. The optimal conditions to construct the biosensor were obtained from an experimental design based on the response surfaces methodology. The GCE/CRGO-βCD/ADA-SPE/AuNPs biosensor exhibited a very good analytical performance for the quantification of eugenol. Thus, it shows a linear range between 1.3 × 10−8 and 1 × 10−5 mol L−1, with a sensitivity of (5.3 ± 0.3) x 10−3 A mol−1 L. The limits of detection and quantification were 4 × 10−9 mol L−1 and 1.3 × 10−8 mol L−1, respectively. Biosensors had an intraday and inter day reproducibility of 5% and 8%, respectively. The repeatability was of 3%, and the stability was 21 days (a decrease of 30% in current responses was observed after the fourth week). Recovery studies were performed in order to validate the proposed method. Recovery percentages were between 94 and 108%. A value of the apparent Michaellis-Menten constant, KMapp, of 3.1 × 10−6 mol L−1 was obtained using both Lineweaver-Burk and Eadi-Hofstee methods. [Display omitted] •An enzymatic biosensor to determine eugenol in dental samples is proposed.•Soybean peroxidase enzyme is used as the biological component.•Supramolecular chemistry is explored.•The working electrodes are modified glassy carbon electrodes.•Chemically reduced graphene oxide is used.
ArticleNumber 120647
Author Lopez, Jimena Claudia
Zon, María Alicia
Fernández, Héctor
Granero, Adrian Marcelo
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Keywords Soybean peroxidase enzyme
β-Cyclodextrin′s
Chemically reduced graphene oxide
Eugenol
Enzymatic biosensor
Language English
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Snippet A GCE/CRGO-βCD′s/ADA-SPE/AuNPs biosensor was successfully developed to determine eugenol in dental samples. The optimal conditions to construct the biosensor...
A GCE/CRGO-βCD's/ADA-SPE/AuNPs biosensor was successfully developed to determine eugenol in dental samples. The optimal conditions to construct the biosensor...
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SubjectTerms Chemically reduced graphene oxide
Enzymatic biosensor
Eugenol
Soybean peroxidase enzyme
β-Cyclodextrin′s
Title Development of an enzymatic biosensor to determine eugenol in dental samples
URI https://dx.doi.org/10.1016/j.talanta.2019.120647
https://www.ncbi.nlm.nih.gov/pubmed/31987210
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