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Effective determination of trace residues of glibenclamide in urine samples using dispersive micro solid-phase extraction and its final detection by chromatographic analysis
被引:13
作者:
Eilami, Owrang
[1
]
Asfaram, Arash
[2
]
Ghaedi, Mehrorang
[3
]
Goudarzi, Alireza
[4
]
机构:
[1] Yasuj Univ Med Sci, Coll Med, Dept Infect Dis & Trop Med, Yasuj, Iran
[2] Yasuj Univ Med Sci, Med Plants Res Ctr, Yasuj, Iran
[3] Univ Yasuj, Dept Chem, Yasuj 7591874831, Iran
[4] Golestan Univ, Dept Polymer Engn, Gorgan 4918888369, Iran
关键词:
LIQUID-LIQUID MICROEXTRACTION;
MOLECULARLY IMPRINTED POLYMER;
QUANTITATIVE-DETERMINATION;
HUMAN PLASMA;
HPLC METHOD;
PRECONCENTRATION;
NANOPARTICLES;
WATER;
GLIMEPIRIDE;
ADSORPTION;
D O I:
10.1039/c8ay01965g
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
An analytical procedure for rapid and effective dispersive micro-solid-phase extraction (DMSPE) of glibenclamide (GB) from urine samples was set up by using sulfur doped tin oxide nanoparticles (S@ SnO2-NPs) loaded on activated carbon (AC), as the sorbent, and clean-up materials, followed by detection. The main experimental parameters affecting the extraction efficiency for GB were assessed and optimized. The maximum recovery of GB predicted by optimization plots was 98.86%, obtained with 15 mL of water, 250 mL of methanol (as an eluent), pH 8.0, 25 mg of S@ SnO2-NPs-AC, and an extraction time of 2.5 min. Our results indicated that under these optimized extraction conditions, determination coefficients (R-2) of the calibration curves in the range of 0.60-5500 mg L-1 were > 0.991, detection limits (signal-to-noise ratio = 3) were in the range of 0.09-0.16 mg L-1, the average recoveries of spiked GB in urine samples were 95.73-105.50%, and assessed relative standard deviations (RSDs, %) were between 1.15 and 6.84%. The results also demonstrated that the presented method could be suitable for the determination of trace residues of GB in urine samples.
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页码:627 / 634
页数:8
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