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Nitrogen- and sulfur-doped carbon dots as peroxidase mimetics: colorimetric determination of hydrogen peroxide and glutathione, and fluorimetric determination of lead(II).
Tang, Mingyu; Zhu, Baoya; Wang, Ying; Wu, Hongbo; Chai, Fang; Qu, Fengyu; Su, Zhongmin.
  • Tang M; Key Laboratory of Photochemical Biomaterials and Energy Storage Materials, Heilongjiang Province; College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, People's Republic of China.
  • Zhu B; Key Laboratory for Photonic and Electronic Bandgap Materials, Ministry of Education, Harbin Normal University, Harbin, 150025, People's Republic of China.
  • Wang Y; Key Laboratory of Photochemical Biomaterials and Energy Storage Materials, Heilongjiang Province; College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, People's Republic of China.
  • Wu H; Key Laboratory for Photonic and Electronic Bandgap Materials, Ministry of Education, Harbin Normal University, Harbin, 150025, People's Republic of China.
  • Chai F; Key Laboratory of Photochemical Biomaterials and Energy Storage Materials, Heilongjiang Province; College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, People's Republic of China.
  • Qu F; Key Laboratory for Photonic and Electronic Bandgap Materials, Ministry of Education, Harbin Normal University, Harbin, 150025, People's Republic of China.
  • Su Z; Key Laboratory of Photochemical Biomaterials and Energy Storage Materials, Heilongjiang Province; College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, People's Republic of China.
Mikrochim Acta ; 186(9): 604, 2019 08 05.
Article en En | MEDLINE | ID: mdl-31385065
ABSTRACT
Fluorescent carbon dots co-doped with nitrogen and sulfur (N/S CDs) were prepared and found to display viable peroxidase mimicking activity. They have a blue fluorescence (with excitation/emission maxima at 340/456 nm) with a quantum yield of 35%. The N/S CDs catalyze the oxidation of 3,3,5,5-tetramethylbenzidine (TMB) in the presence of H2O2, and this leads to the appearance of a blue solution with a absorption maximum at 654 nm. A colorimetric method was developed for the determination of H2O2 that has a 1.75 µM detection limit and a linear response in the 10-5 to 10-4 M concentration range. The method can be extended to the enzymatic determination of glutathione with a 0.26 µM detection limit and a working range from 0.20 to 100 µM. In addition, the CDs respond to lead(II) which is a quencher of the blue fluorescence at 456 nm, with a detection limit of 11 µM and a working range up to 100 µM. Simultaneously, the color changes can be visually detected with absorbance signal changes from 10 to 100 µM with limit of 3.9 µM. A multiple detection system was worked out that allows monitoring of H2O2 and glutathione successively, and of lead(II). Graphical abstract (A) Schematic representation of the nitrogen & sulphur doped carbon dots with blue fluorescence, (B) the peroxidase-like activity in colorimetric detecting of H2O2 and GSH and (C) the illustration for the application of Pb2+ detection with fluorescence and colorimetric method.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2019 Tipo del documento: Article