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Synthesis and Characterization of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized Silver Nanoparticles: Dual Colorimetric Sensors of Zn(2+) and Homocysteine
[Image: see text] A colorimetric assay has been developed for Zn(2+) and homocysteine (Hcy) detection using functionalized silver nanoparticles (AgNPs). AgNPs have been synthesized using silver nitrate, where sodium citrate is used as a stabilizing agent and NaBH(4) as a reducing agent. Then, the na...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494438/ https://www.ncbi.nlm.nih.gov/pubmed/36157721 http://dx.doi.org/10.1021/acsomega.2c04165 |
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author | Mondal, Palash Yarger, Jeffery L. |
author_facet | Mondal, Palash Yarger, Jeffery L. |
author_sort | Mondal, Palash |
collection | PubMed |
description | [Image: see text] A colorimetric assay has been developed for Zn(2+) and homocysteine (Hcy) detection using functionalized silver nanoparticles (AgNPs). AgNPs have been synthesized using silver nitrate, where sodium citrate is used as a stabilizing agent and NaBH(4) as a reducing agent. Then, the nanoparticles (citrate@AgNPs) were functionalized with 1H-imidazole-4,5-dicarboxylic acid (IDCA). UV–visible and FTIR spectra suggested that IDCA was functionalized on the surface of citrate@AgNPs through the N atom of the imidazole ring. The IDCA-functionalized silver nanoparticles (IDCA@AgNPs) simultaneously detected Zn(2+) and Hcy from aqueous solution and showed different responses to the two analytes (Zn(2+) and Hcy) based on the aggregation-induced color change of IDCA@AgNPs. They showed the color change from yellow to red, which was easily discriminated by visual inspection as well as UV–visible spectroscopy. The surface plasmon resonance absorbance values of Zn(2+) and Hcy are 485 and 512 nm, respectively, when Zn(2+) and Hcy react with IDCA@AgNPs. IDCA@AgNPs showed linearity with Zn(2+) and Hcy concentrations, with the detection limit of 2.38 μM and 0.54 nM, respectively (S/N = 3). The IDCA@AgNPs showed excellent selectivity toward Zn(2+) and Hcy compared to the different metal ions and amino acids, respectively. Optimal detection was achieved toward Zn(2+) and Hcy in the pH range 3–10. In addition, IDCA@AgNPs were used to detect Zn(2+) and Hcy from lake water, showing low interference. |
format | Online Article Text |
id | pubmed-9494438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94944382022-09-23 Synthesis and Characterization of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized Silver Nanoparticles: Dual Colorimetric Sensors of Zn(2+) and Homocysteine Mondal, Palash Yarger, Jeffery L. ACS Omega [Image: see text] A colorimetric assay has been developed for Zn(2+) and homocysteine (Hcy) detection using functionalized silver nanoparticles (AgNPs). AgNPs have been synthesized using silver nitrate, where sodium citrate is used as a stabilizing agent and NaBH(4) as a reducing agent. Then, the nanoparticles (citrate@AgNPs) were functionalized with 1H-imidazole-4,5-dicarboxylic acid (IDCA). UV–visible and FTIR spectra suggested that IDCA was functionalized on the surface of citrate@AgNPs through the N atom of the imidazole ring. The IDCA-functionalized silver nanoparticles (IDCA@AgNPs) simultaneously detected Zn(2+) and Hcy from aqueous solution and showed different responses to the two analytes (Zn(2+) and Hcy) based on the aggregation-induced color change of IDCA@AgNPs. They showed the color change from yellow to red, which was easily discriminated by visual inspection as well as UV–visible spectroscopy. The surface plasmon resonance absorbance values of Zn(2+) and Hcy are 485 and 512 nm, respectively, when Zn(2+) and Hcy react with IDCA@AgNPs. IDCA@AgNPs showed linearity with Zn(2+) and Hcy concentrations, with the detection limit of 2.38 μM and 0.54 nM, respectively (S/N = 3). The IDCA@AgNPs showed excellent selectivity toward Zn(2+) and Hcy compared to the different metal ions and amino acids, respectively. Optimal detection was achieved toward Zn(2+) and Hcy in the pH range 3–10. In addition, IDCA@AgNPs were used to detect Zn(2+) and Hcy from lake water, showing low interference. American Chemical Society 2022-09-07 /pmc/articles/PMC9494438/ /pubmed/36157721 http://dx.doi.org/10.1021/acsomega.2c04165 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Mondal, Palash Yarger, Jeffery L. Synthesis and Characterization of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized Silver Nanoparticles: Dual Colorimetric Sensors of Zn(2+) and Homocysteine |
title | Synthesis and Characterization
of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized
Silver Nanoparticles:
Dual Colorimetric Sensors of Zn(2+) and Homocysteine |
title_full | Synthesis and Characterization
of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized
Silver Nanoparticles:
Dual Colorimetric Sensors of Zn(2+) and Homocysteine |
title_fullStr | Synthesis and Characterization
of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized
Silver Nanoparticles:
Dual Colorimetric Sensors of Zn(2+) and Homocysteine |
title_full_unstemmed | Synthesis and Characterization
of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized
Silver Nanoparticles:
Dual Colorimetric Sensors of Zn(2+) and Homocysteine |
title_short | Synthesis and Characterization
of 1H-Imidazole-4,5-dicarboxylic Acid-Functionalized
Silver Nanoparticles:
Dual Colorimetric Sensors of Zn(2+) and Homocysteine |
title_sort | synthesis and characterization
of 1h-imidazole-4,5-dicarboxylic acid-functionalized
silver nanoparticles:
dual colorimetric sensors of zn(2+) and homocysteine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494438/ https://www.ncbi.nlm.nih.gov/pubmed/36157721 http://dx.doi.org/10.1021/acsomega.2c04165 |
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