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Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection

We report fabrication of new generation nanoflowers (NFs) using gallic acid (GA) and copper (II) ions (Cu(2+)) acted as an organic and inorganic component, respectively with effective peroxidase mimic activities in solution and on filter membrane. Unlike the typical protein NFs synthesis mechanism,...

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Autores principales: Dadi, Seyma, Celik, Cagla, Ocsoy, Ismail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542149/
https://www.ncbi.nlm.nih.gov/pubmed/33028883
http://dx.doi.org/10.1038/s41598-020-73778-7
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author Dadi, Seyma
Celik, Cagla
Ocsoy, Ismail
author_facet Dadi, Seyma
Celik, Cagla
Ocsoy, Ismail
author_sort Dadi, Seyma
collection PubMed
description We report fabrication of new generation nanoflowers (NFs) using gallic acid (GA) and copper (II) ions (Cu(2+)) acted as an organic and inorganic component, respectively with effective peroxidase mimic activities in solution and on filter membrane. Unlike the typical protein NFs synthesis mechanism, gallic acid NFs (GA-NFs) was formed via coordination reaction between carboxyl groups of GA and Cu(2+). The different morphologies of the GA-NFs were acquired based upon whether the carboxyl groups in gallic acid are active or not. The peroxidase mimic activity of the GA-NFs relied on the Fenton reaction in the presence of hydrogen peroxide (H(2)O(2)) was tested towards m-cresol as a function of concentration of the GA-NFs, m-cresol, H(2)O(2) and reaction time. Under the optimized conditions, the oxidative coupling of m-cresol with 4-aminoantipyrine (4-AAP) was catalyzed by the GA-NFs dispersed in solution and adsorbed on filter paper to form an antipyrine dye and it was visually and spectrophotometrically recorded. The m-cresol with range of 0.05–0.5 mM was detected in 10 min and 15 min by using the GA-NFs in solution and on filter paper, respectively. We demonstrated that the NFs can be produced from non-protein molecules and GA-NFs can be used as a promising nanocatalyst for a variety of applications.
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spelling pubmed-75421492020-10-08 Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection Dadi, Seyma Celik, Cagla Ocsoy, Ismail Sci Rep Article We report fabrication of new generation nanoflowers (NFs) using gallic acid (GA) and copper (II) ions (Cu(2+)) acted as an organic and inorganic component, respectively with effective peroxidase mimic activities in solution and on filter membrane. Unlike the typical protein NFs synthesis mechanism, gallic acid NFs (GA-NFs) was formed via coordination reaction between carboxyl groups of GA and Cu(2+). The different morphologies of the GA-NFs were acquired based upon whether the carboxyl groups in gallic acid are active or not. The peroxidase mimic activity of the GA-NFs relied on the Fenton reaction in the presence of hydrogen peroxide (H(2)O(2)) was tested towards m-cresol as a function of concentration of the GA-NFs, m-cresol, H(2)O(2) and reaction time. Under the optimized conditions, the oxidative coupling of m-cresol with 4-aminoantipyrine (4-AAP) was catalyzed by the GA-NFs dispersed in solution and adsorbed on filter paper to form an antipyrine dye and it was visually and spectrophotometrically recorded. The m-cresol with range of 0.05–0.5 mM was detected in 10 min and 15 min by using the GA-NFs in solution and on filter paper, respectively. We demonstrated that the NFs can be produced from non-protein molecules and GA-NFs can be used as a promising nanocatalyst for a variety of applications. Nature Publishing Group UK 2020-10-07 /pmc/articles/PMC7542149/ /pubmed/33028883 http://dx.doi.org/10.1038/s41598-020-73778-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dadi, Seyma
Celik, Cagla
Ocsoy, Ismail
Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection
title Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection
title_full Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection
title_fullStr Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection
title_full_unstemmed Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection
title_short Gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection
title_sort gallic acid nanoflower immobilized membrane with peroxidase-like activity for m-cresol detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542149/
https://www.ncbi.nlm.nih.gov/pubmed/33028883
http://dx.doi.org/10.1038/s41598-020-73778-7
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AT ocsoyismail gallicacidnanoflowerimmobilizedmembranewithperoxidaselikeactivityformcresoldetection