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Development of a Nonenzymatic Colorimetric Sensor for the Detection of Uric Acid Based on Ionic Liquid-Mediated Nickel Nanostructures
[Image: see text] Uric acid (UA) is a metabolic byproduct of purine nucleotides and is excreted as a urine component. Abnormalities in UA metabolism cause localized inflammation due to crystal deposition and can lead to various diseases. In the current study, we successfully fabricated a biosensor b...
Autores principales: | , , , , , , , , |
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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/PMC9352337/ https://www.ncbi.nlm.nih.gov/pubmed/35936421 http://dx.doi.org/10.1021/acsomega.2c04070 |
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author | Nishan, Umar Ullah, Wajid Muhammad, Nawshad Asad, Muhammad Afridi, Saifullah Khan, Muslim Shah, Mohibullah Khan, Naeem Rahim, Abdur |
author_facet | Nishan, Umar Ullah, Wajid Muhammad, Nawshad Asad, Muhammad Afridi, Saifullah Khan, Muslim Shah, Mohibullah Khan, Naeem Rahim, Abdur |
author_sort | Nishan, Umar |
collection | PubMed |
description | [Image: see text] Uric acid (UA) is a metabolic byproduct of purine nucleotides and is excreted as a urine component. Abnormalities in UA metabolism cause localized inflammation due to crystal deposition and can lead to various diseases. In the current study, we successfully fabricated a biosensor based on 1-H-3-methylimidazolium acetate (ionic liquid, IL)-capped nickel nanoparticles (NiNPs) for the detection of uric acid in test samples. The structures of IL-capped NiNPs and their precursors were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction. The IL-capped NiNPs possessed intrinsic peroxidase-like properties and displayed selective UA quenching after interacting with 3,3′,5,5′-tetramethylbenzidine (TMB) solution. Different parameters such as pH, time, IL, TMB, and UA concentration were optimized to obtain the best results for the proposed sensor. The UA biosensor shows good responses in the linear range from 1 × 10(–8) to 2.40 × 10(–6) M, with a lower limit of detection of 1.30 × 10(–7) M, a limit of quantification of 4.3 × 10(–7) M, and an R(2) value of 0.9994. For the colorimetric detection of UA, the proposed sensor gave a short time response of 4 min at room temperature and pH 7.5. The proposed sensing probe detects UA in real serum samples and could be used as a selective sensor for UA in the real sample detection. |
format | Online Article Text |
id | pubmed-9352337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93523372022-08-05 Development of a Nonenzymatic Colorimetric Sensor for the Detection of Uric Acid Based on Ionic Liquid-Mediated Nickel Nanostructures Nishan, Umar Ullah, Wajid Muhammad, Nawshad Asad, Muhammad Afridi, Saifullah Khan, Muslim Shah, Mohibullah Khan, Naeem Rahim, Abdur ACS Omega [Image: see text] Uric acid (UA) is a metabolic byproduct of purine nucleotides and is excreted as a urine component. Abnormalities in UA metabolism cause localized inflammation due to crystal deposition and can lead to various diseases. In the current study, we successfully fabricated a biosensor based on 1-H-3-methylimidazolium acetate (ionic liquid, IL)-capped nickel nanoparticles (NiNPs) for the detection of uric acid in test samples. The structures of IL-capped NiNPs and their precursors were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction. The IL-capped NiNPs possessed intrinsic peroxidase-like properties and displayed selective UA quenching after interacting with 3,3′,5,5′-tetramethylbenzidine (TMB) solution. Different parameters such as pH, time, IL, TMB, and UA concentration were optimized to obtain the best results for the proposed sensor. The UA biosensor shows good responses in the linear range from 1 × 10(–8) to 2.40 × 10(–6) M, with a lower limit of detection of 1.30 × 10(–7) M, a limit of quantification of 4.3 × 10(–7) M, and an R(2) value of 0.9994. For the colorimetric detection of UA, the proposed sensor gave a short time response of 4 min at room temperature and pH 7.5. The proposed sensing probe detects UA in real serum samples and could be used as a selective sensor for UA in the real sample detection. American Chemical Society 2022-07-20 /pmc/articles/PMC9352337/ /pubmed/35936421 http://dx.doi.org/10.1021/acsomega.2c04070 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 | Nishan, Umar Ullah, Wajid Muhammad, Nawshad Asad, Muhammad Afridi, Saifullah Khan, Muslim Shah, Mohibullah Khan, Naeem Rahim, Abdur Development of a Nonenzymatic Colorimetric Sensor for the Detection of Uric Acid Based on Ionic Liquid-Mediated Nickel Nanostructures |
title | Development of
a Nonenzymatic Colorimetric Sensor
for the Detection of Uric Acid Based on Ionic
Liquid-Mediated Nickel Nanostructures |
title_full | Development of
a Nonenzymatic Colorimetric Sensor
for the Detection of Uric Acid Based on Ionic
Liquid-Mediated Nickel Nanostructures |
title_fullStr | Development of
a Nonenzymatic Colorimetric Sensor
for the Detection of Uric Acid Based on Ionic
Liquid-Mediated Nickel Nanostructures |
title_full_unstemmed | Development of
a Nonenzymatic Colorimetric Sensor
for the Detection of Uric Acid Based on Ionic
Liquid-Mediated Nickel Nanostructures |
title_short | Development of
a Nonenzymatic Colorimetric Sensor
for the Detection of Uric Acid Based on Ionic
Liquid-Mediated Nickel Nanostructures |
title_sort | development of
a nonenzymatic colorimetric sensor
for the detection of uric acid based on ionic
liquid-mediated nickel nanostructures |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352337/ https://www.ncbi.nlm.nih.gov/pubmed/35936421 http://dx.doi.org/10.1021/acsomega.2c04070 |
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