Sensitive analysis of aminoglycoside antibiotics via hyphenation of transient moving substitution boundary with field-enhanced sample injection in capillary electrophoresis

•A novel FESI-MSB method in CE-AD was developed.•The mechanism of MSB relied on substitution reaction between 18C6H4-AGs and Na+.•18C6H4 proved to be a novel PSP for analytes with primary amine groups focusing.•This strategy afforded about 400–1000-fold improvements in detection sensitivity. A novel...

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Published in:Journal of Chromatography A Vol. 1295; pp. 128 - 135
Main Authors: Ge, Shuli, Tang, Wanrong, Han, Ruobing, Zhu, Yan, Wang, Qingjiang, He, Pingang, Fang, Yuzhi
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 21-06-2013
Elsevier
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Summary:•A novel FESI-MSB method in CE-AD was developed.•The mechanism of MSB relied on substitution reaction between 18C6H4-AGs and Na+.•18C6H4 proved to be a novel PSP for analytes with primary amine groups focusing.•This strategy afforded about 400–1000-fold improvements in detection sensitivity. A novel field-enhanced sample injection coupled with transient moving substitution boundary method in capillary electrophoresis was developed for aminoglycoside antibiotic (AG) analysis using 18-crown-6-tetracarboxylic acid (18C6H4) as a pseudostationary phase. Results indicated that the stacking mechanism of moving substitution boundary relied on the substitution reaction between 18C6H4-bonded AG complexes and Na+ at the substitution boundary. The stacking mechanism as well as important parameters governing pre-concentration and separation have been investigated in order to obtain maximum resolution and sensitivity. Under optimized conditions, using a sample prepared in a low-conductivity matrix, the limits of detection for streptomycin, neomycin, and kanamycin were 0.62, 5.9 and 8.6nM (S/N=3), respectively, and the detection sensitivities were improved 940-, 692-, and 415-fold, respectively. The method also gave accurate and reliable results in the analysis of AGs in river water samples.
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ISSN:0021-9673
1873-3778
DOI:10.1016/j.chroma.2013.04.049