| Literature DB >> 28961529 |
Ji Yang1, Zheng-Zhong Lin1, A-Zha Nur1, Yan Lu1, Ming-Hui Wu2, Jun Zeng1, Xiao-Mei Chen1, Zhi-Yong Huang3.
Abstract
A novel fluorescence-based sensor combining synchronous fluorescence spectroscopy (SFS) with molecularly imprinted polymers (MIPs) was fabricated with reverse microemulsion method. Tetracycline (TC), (3-aminopropyl) triethoxysilane (APTES), tetraethyl orthosilicate (TEOS) and carbon quantum dots (CDs) were used as template, functional monomer, cross-linker and signal sources respectively in the probe preparation. A synchronous fluorescence emission (λem) at 355nm was observed for the prepared MIP-coated CDs (MIP@CDs) particles when the wavelength interval (Δλ) was set as 70nm, and the synchronous fluorescence intensity could be rapidly and efficiently quenched by TC based on inner filter effect (IFE). The quenching efficiencies of synchronous fluorescence intensity was linearly fitted with tetracycline (TC) concentrations ranging from 0.1 to 50μmolL-1 with a detection limit (DL) of 9nmolL-1 (3σ, n=9). The MIP@CDs was used as a probe to detect TC in fish samples with the recoveries ranging from 98.4% to 103.1% and the relative standard deviation less than 6.0%. The results illustrated that the as-prepared MIP@CDs could be applied to the detection of trace TC in fish samples with rapidity, high sensitivity and accuracy.Entities:
Keywords: Carbon dots; Fish; Inner filter effect; Molecularly imprinted polymers; Synchronous fluorescence spectroscopy; Tetracycline
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Year: 2017 PMID: 28961529 DOI: 10.1016/j.saa.2017.09.066
Source DB: PubMed Journal: Spectrochim Acta A Mol Biomol Spectrosc ISSN: 1386-1425 Impact factor: 4.098