Green Emission Carbon Nanodots as Fluorescence Turn-on Probe for Detecting Picolinic Acid

A new strategy for the determination of picolinic acid ( PLA ) is developed by utilizing green-emissive boron and nitrogen co-doped carbon nanodots ( BNCNDs ) and Cu 2+ ion. Hydroquinone, uric acid and boric acid act as carbon, nitrogen and boron sources for BNCNDs synthesis, respectively. Interesti...

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Published inJournal of analytical chemistry (New York, N.Y.) Vol. 76; no. 8; pp. 920 - 929
Main Authors Ding, Yu-Jie, Jin, Xing, Wang, Zhong-Xia, Wang, Wei
Format Journal Article
LanguageEnglish
Published Moscow Pleiades Publishing 01.08.2021
Springer
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Abstract A new strategy for the determination of picolinic acid ( PLA ) is developed by utilizing green-emissive boron and nitrogen co-doped carbon nanodots ( BNCNDs ) and Cu 2+ ion. Hydroquinone, uric acid and boric acid act as carbon, nitrogen and boron sources for BNCNDs synthesis, respectively. Interestingly, the green emission of BNCNDs is quenched in the presence of Cu 2+ by electron transfer. Upon addition of the specific reagent ( PLA ), Cu 2+ ion is removed from the surface of BNCNDs owing to the formation of a strong complex between PLA and Cu 2+ ion, which leads to a significant fluorescence recovery of BNCNDs. The “turn-on” phenomenon allows to determine PLA by a very simple method. This chemosensing method displays a linear range from 50 nM to 80 μM with a detection limit of 14 nM (3σ/ k ) for PLA. The method was applied to the determination of PLA in fetal bovine serum samples with the recoveries between 94 and 106%, which shows that this method has potential for use in applications to real samples.
AbstractList A new strategy for the determination of picolinic acid (PLA) is developed by utilizing green-emissive boron and nitrogen co-doped carbon nanodots (BNCNDs) and Cu.sup.2+ ion. Hydroquinone, uric acid and boric acid act as carbon, nitrogen and boron sources for BNCNDs synthesis, respectively. Interestingly, the green emission of BNCNDs is quenched in the presence of Cu.sup.2+ by electron transfer. Upon addition of the specific reagent (PLA), Cu.sup.2+ ion is removed from the surface of BNCNDs owing to the formation of a strong complex between PLA and Cu.sup.2+ ion, which leads to a significant fluorescence recovery of BNCNDs. The "turn-on" phenomenon allows to determine PLA by a very simple method. This chemosensing method displays a linear range from 50 nM to 80 [mu]M with a detection limit of 14 nM (3[sigma]/k) for PLA. The method was applied to the determination of PLA in fetal bovine serum samples with the recoveries between 94 and 106%, which shows that this method has potential for use in applications to real samples.
A new strategy for the determination of picolinic acid (PLA) is developed by utilizing green-emissive boron and nitrogen co-doped carbon nanodots (BNCNDs) and Cu2+ ion. Hydroquinone, uric acid and boric acid act as carbon, nitrogen and boron sources for BNCNDs synthesis, respectively. Interestingly, the green emission of BNCNDs is quenched in the presence of Cu2+ by electron transfer. Upon addition of the specific reagent (PLA), Cu2+ ion is removed from the surface of BNCNDs owing to the formation of a strong complex between PLA and Cu2+ ion, which leads to a significant fluorescence recovery of BNCNDs. The “turn-on” phenomenon allows to determine PLA by a very simple method. This chemosensing method displays a linear range from 50 nM to 80 μM with a detection limit of 14 nM (3σ/k) for PLA. The method was applied to the determination of PLA in fetal bovine serum samples with the recoveries between 94 and 106%, which shows that this method has potential for use in applications to real samples.
A new strategy for the determination of picolinic acid ( PLA ) is developed by utilizing green-emissive boron and nitrogen co-doped carbon nanodots ( BNCNDs ) and Cu 2+ ion. Hydroquinone, uric acid and boric acid act as carbon, nitrogen and boron sources for BNCNDs synthesis, respectively. Interestingly, the green emission of BNCNDs is quenched in the presence of Cu 2+ by electron transfer. Upon addition of the specific reagent ( PLA ), Cu 2+ ion is removed from the surface of BNCNDs owing to the formation of a strong complex between PLA and Cu 2+ ion, which leads to a significant fluorescence recovery of BNCNDs. The “turn-on” phenomenon allows to determine PLA by a very simple method. This chemosensing method displays a linear range from 50 nM to 80 μM with a detection limit of 14 nM (3σ/ k ) for PLA. The method was applied to the determination of PLA in fetal bovine serum samples with the recoveries between 94 and 106%, which shows that this method has potential for use in applications to real samples.
Audience Academic
Author Ding, Yu-Jie
Wang, Wei
Wang, Zhong-Xia
Jin, Xing
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  email: wangw@ycit.edu.cn
  organization: School of Chemistry and Chemical Engineering, Yancheng Institute of Technology
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Copyright Pleiades Publishing, Ltd. 2021. ISSN 1061-9348, Journal of Analytical Chemistry, 2021, Vol. 76, No. 8, pp. 920–929. © Pleiades Publishing, Ltd., 2021.
COPYRIGHT 2021 Springer
Copyright_xml – notice: Pleiades Publishing, Ltd. 2021. ISSN 1061-9348, Journal of Analytical Chemistry, 2021, Vol. 76, No. 8, pp. 920–929. © Pleiades Publishing, Ltd., 2021.
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Keywords carbon nanodots
picolinic acid
sensor
photoluminescence
Cu(II)
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Snippet A new strategy for the determination of picolinic acid ( PLA ) is developed by utilizing green-emissive boron and nitrogen co-doped carbon nanodots ( BNCNDs )...
A new strategy for the determination of picolinic acid (PLA) is developed by utilizing green-emissive boron and nitrogen co-doped carbon nanodots (BNCNDs) and...
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SubjectTerms Acids
Analytical Chemistry
Boric acid
Boron
Carbon
Chemistry
Chemistry and Materials Science
Copper
Electron transfer
Electron transport
Emission spectra
Fluorescence
Hydroquinone
Investigations
Reagents
Uric acid
Title Green Emission Carbon Nanodots as Fluorescence Turn-on Probe for Detecting Picolinic Acid
URI https://link.springer.com/article/10.1134/S1061934821080037
https://www.proquest.com/docview/2556409086/abstract/
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