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A Simple and Rapid Phosphorescence Probe Based on Mn-Doped ZnS Quantum Dots for Chloramphenicol Detection.

Authors :
Liu, Zhenping
Wang, Xianfeng
Hou, Jingzhou
Huo, Danqun
Hou, Changjun
Source :
NANO. Nov2019, Vol. 14 Issue 11, pN.PAG-N.PAG. 10p.
Publication Year :
2019

Abstract

An innovative phosphorescence probe based on Mn-doped ZnS quantum dots (Mn:ZnS QDs) was developed for selective detection of chloramphenicol (CAP) via inner-filter effect (IFE). Mn:ZnS QDs were synthesized by water method and modified with L-Cysteine for better stability, and the average diameter of the nanometer particle was 3.8 nm. With the excitation wavelength at 289 nm, the strong phosphorescence of Mn:ZnS QDs can be emitted at 583 nm. The excitation spectrum of Mn:ZnS QDs was substantially overlapped with the absorption spectrum of the target CAP. The excited light of Mn:ZnS QDs can be absorbed partially by CAP when they coexist, the phosphorescence intensity decreased with the increasing concentration of CAP, and it has a good linear relationship. Under optimal conditions, the linear relational concentration range achieved four orders of magnitude from 25 to 1. 2 × 1 0 5 ng ⋅ mL − 1 ( R 2 = 0. 9 9 9), with a detection limit (LOD; S ∕ N = 3) down to 0.81 ng ⋅ mL − 1 . The simple, rapid and low cost IFE phosphorescent probe exhibited satisfactory recoveries ranging from 88.9% to 98.5% for CAP analysis in spiked honey, which shows a potential for routine screening of CAP in ensuring the food safety. A phosphorescence probe for the detection of chloramphenicol (CAP) was established by using the internal filtration effect (IFE) of CAP on the room temperature phosphorescence signal of manganese-doped ZnS quantum dots (Mn:ZnS QDs). The quantitative detection of CAP can be realized by simply mixing the QDs solution with the solution of the samples to be tested. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17932920
Volume :
14
Issue :
11
Database :
Academic Search Index
Journal :
NANO
Publication Type :
Academic Journal
Accession number :
139888134
Full Text :
https://doi.org/10.1142/S1793292019501443