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Sulfur/nitrogen co-doped carbon-based copper nanozyme with high peroxidase-like activity for dual-channel paper-based detection of melatonin.

Authors :
Zhou, Chenyu
Wang, Nan
Su, Yu
Liu, Junxue
Lv, Yuntai
Su, Xingguang
Source :
Sensors & Actuators B: Chemical. Nov2024, Vol. 418, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Multiple heteroatom doping is one of the effective strategies to tune the structure of carbon supports and enhance the catalytic performance of nanozymes. Herein, the carbon-based copper nanozyme with sulfur/nitrogen co-doping (S/Cu-NC) was synthesized by one-step pyrolysis of Cu-doped ZIF-8 with thiourea encapsulated (Th/Cu@ZIF-8). Benefiting from the synergy of binary heteroatoms and 3D porous structure, the obtained S/Cu-NC had more active sites and exhibited outstanding peroxidase-like activity. Subsequently, a dual-channel (colorimetric/fluorescent) detection method for melatonin was developed by selecting 3,3,5,5-tetramethylbenzidine (TMB) and thiamine as the substrates of S/Cu-NC, which was based on the free radical scavenging effect of melatonin. Furthermore, a simple and portable paper-based device was designed to realize the rapid detection of melatonin through color changes under ultraviolet light and daylight, and the limit of detection were 0.87 μM and 1.42 μM, respectively. This paper-based device was successfully applied to detect melatonin in two kinds of drug samples with satisfactory results. • The carbon-based copper nanozyme with S/N co-doping (S/Cu-NC) was synthesized by one-step pyrolysis. • S/Cu-NC exhibited enhanced peroxidase-like activity due to more activity sites brought by heteroatoms. • A portable paper-based device was constructed to realize the dual-channel rapid detection of melatonin. • The portable paper-based device was used to detection melatonin in two types of drug samples. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09254005
Volume :
418
Database :
Academic Search Index
Journal :
Sensors & Actuators B: Chemical
Publication Type :
Academic Journal
Accession number :
178939860
Full Text :
https://doi.org/10.1016/j.snb.2024.136246