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CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase

[Image: see text] Manganese dioxide (MnO(2)) nanosheet-based fluorescence sensors often use oxidase-like activity or wide absorption spectrum for detection of antioxidants. In those strategies, MnO(2) nanosheets were reduced to Mn(2+) by antioxidants. However, few strategies emphasize the role of Mn...

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Autores principales: Lu, Hongzhi, Xu, Shoufang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246696/
https://www.ncbi.nlm.nih.gov/pubmed/34235328
http://dx.doi.org/10.1021/acsomega.1c01828
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author Lu, Hongzhi
Xu, Shoufang
author_facet Lu, Hongzhi
Xu, Shoufang
author_sort Lu, Hongzhi
collection PubMed
description [Image: see text] Manganese dioxide (MnO(2)) nanosheet-based fluorescence sensors often use oxidase-like activity or wide absorption spectrum for detection of antioxidants. In those strategies, MnO(2) nanosheets were reduced to Mn(2+) by antioxidants. However, few strategies emphasize the role of Mn(2+) obtained from MnO(2) reduction in the design of the fluorescence sensor. Herein, we expanded the application of a MnO(2) nanosheet-based fluorescence sensor by involving Mn(2+) in the detection process using ascorbic acid (AA) as a model target. In this strategy, carbon dots (CDs), MnO(2) nanosheets, and tetraphenylporphyrin tetrasulfonic acid (TPPS) comprise a ternary system for ratiometric fluorescence detection of AA. Initially, CDs were quenched by MnO(2) nanosheets based on the inner filter effect, while TPPS maintained its fluorescence intensity. After the addition of AA, MnO(2) nanosheets were reduced to Mn(2+) so that the fluorescence intensity of CDs was recovered and TTPS was quenched by coordination with Mn(2+). Overall, AA triggered an emission intensity increase at 440 nm for CDs and a decrease at 640 nm for TPPS. The ratio intensity of CDs to TPPS (F(440)/F(640)) showed a good linear relationship from 0.5 to 40 μM, with a low detection limit of 0.13 μM for AA detection. By means of the alkaline phosphatase (ALP)-triggered generation of AA, this strategy can be applied for the detection of ALP in the range of 0.1–100 mU/mL, with a detection limit of 0.04 mU/mL. Furthermore, this sensor was applied to detect AA and ALP in real, complex samples with ideal recovery. This novel platform extended the application of MnO(2) nanosheet-based fluorescence sensors.
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spelling pubmed-82466962021-07-06 CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase Lu, Hongzhi Xu, Shoufang ACS Omega [Image: see text] Manganese dioxide (MnO(2)) nanosheet-based fluorescence sensors often use oxidase-like activity or wide absorption spectrum for detection of antioxidants. In those strategies, MnO(2) nanosheets were reduced to Mn(2+) by antioxidants. However, few strategies emphasize the role of Mn(2+) obtained from MnO(2) reduction in the design of the fluorescence sensor. Herein, we expanded the application of a MnO(2) nanosheet-based fluorescence sensor by involving Mn(2+) in the detection process using ascorbic acid (AA) as a model target. In this strategy, carbon dots (CDs), MnO(2) nanosheets, and tetraphenylporphyrin tetrasulfonic acid (TPPS) comprise a ternary system for ratiometric fluorescence detection of AA. Initially, CDs were quenched by MnO(2) nanosheets based on the inner filter effect, while TPPS maintained its fluorescence intensity. After the addition of AA, MnO(2) nanosheets were reduced to Mn(2+) so that the fluorescence intensity of CDs was recovered and TTPS was quenched by coordination with Mn(2+). Overall, AA triggered an emission intensity increase at 440 nm for CDs and a decrease at 640 nm for TPPS. The ratio intensity of CDs to TPPS (F(440)/F(640)) showed a good linear relationship from 0.5 to 40 μM, with a low detection limit of 0.13 μM for AA detection. By means of the alkaline phosphatase (ALP)-triggered generation of AA, this strategy can be applied for the detection of ALP in the range of 0.1–100 mU/mL, with a detection limit of 0.04 mU/mL. Furthermore, this sensor was applied to detect AA and ALP in real, complex samples with ideal recovery. This novel platform extended the application of MnO(2) nanosheet-based fluorescence sensors. American Chemical Society 2021-06-16 /pmc/articles/PMC8246696/ /pubmed/34235328 http://dx.doi.org/10.1021/acsomega.1c01828 Text en © 2021 The Authors. Published by American Chemical Society 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 Lu, Hongzhi
Xu, Shoufang
CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase
title CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase
title_full CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase
title_fullStr CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase
title_full_unstemmed CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase
title_short CDs–MnO(2)–TPPS Ternary System for Ratiometric Fluorescence Detection of Ascorbic Acid and Alkaline Phosphatase
title_sort cds–mno(2)–tpps ternary system for ratiometric fluorescence detection of ascorbic acid and alkaline phosphatase
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246696/
https://www.ncbi.nlm.nih.gov/pubmed/34235328
http://dx.doi.org/10.1021/acsomega.1c01828
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