Molecularly imprinted polymers on CdS quantum dots for sensitive determination of cefixime after its preconcentration by magnetic graphene oxide
A sensitive and selective method was developed for the simple monitoring of cefixime based on its preconcentration by magnetic Fe 3 O 4 @SiO 2 modified graphene oxide (Fe 3 O 4 @SiO 2 -GO) and fluorimetric detection using molecularly imprinted polymer coated CdS quantum dots (MIP-CdS QDs). GO was si...
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Veröffentlicht in: | New journal of chemistry 2017, Vol.41 (15), p.7186-7194 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A sensitive and selective method was developed for the simple monitoring of cefixime based on its preconcentration by magnetic Fe
3
O
4
@SiO
2
modified graphene oxide (Fe
3
O
4
@SiO
2
-GO) and fluorimetric detection using molecularly imprinted polymer coated CdS quantum dots (MIP-CdS QDs). GO was simply synthesized using the Hummers method and then was modified using Fe
3
O
4
@SiO
2
nanoparticles. MIP-CdS QDs were obtained by copolymerization of certain monomers in the presence of CdS QDs as fluorescent materials and cefixime as a template molecule. The obtained nanomaterials were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and X-ray powder diffraction (XRD). MIP-CdS QDs showed a high tendency towards cefixime, and the adsorbed cefixime molecules led to a linear increase in the emission intensity of QDs. Based on this effect, a selective determination method was designed for cefixime. To detect lower cefixime concentrations, a preconcentration step was applied. In this regard, the dispersed Fe
3
O
4
@SiO
2
-GO displayed good efficiency to extract low amounts of cefixime as a model analyte. Important parameters including pH, buffer type and concentration, reagent amounts, ionic buffer, incubation time, eluent,
etc.
were optimized for both the extraction and detection steps. A calibration graph in the concentration range of 0.001–0.7 μg mL
−1
was obtained for cefixime with a detection limit (3 s) of 0.54 ng mL
−1
. The present method was satisfactorily used for cefixime determination in pharmaceutical and urine samples. The results were shown to possess adequate features compared with previous methods. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/C7NJ00834A |