Title of article :
Penicillin analyses by capillary electrochromatography-mass spectrometry with different charged poly(stearyl methacrylate–divinylbenzene) monoliths as stationary phases
Author/Authors :
Liu، نويسنده , , Wan-Ling and Wu، نويسنده , , Ching-Yi and Li، نويسنده , , Yi-Ting and Huang، نويسنده , , Hsi-Ya، نويسنده ,
Issue Information :
ماهنامه با شماره پیاپی سال 2012
Pages :
7
From page :
71
To page :
77
Abstract :
This study describes the ability of an on-line concentration capillary electrochromatography (CEC) coupled with mass spectrometry (MS) for the determination of eight common penicillin antibiotics. Poly(stearyl methacrylate–divinylbenzene) (poly(SMA–DVB)) based monolithic columns prepared under the same conditions but differing only in the charged monomer were used as separation columns. Vinylbenzyl trimethylammonium chloride (VBTA) and vinylbenzenesulfonate (VBSA) were employed as the positively charged monolith and negatively charged monolith, respectively. Results indicated that poly(SMA–DVB–VBTA) monolithic column provided reproducible performance for penicillin separation through ion-exchange interaction, while the negatively charged poly(SMA–DVB–VBSA) column produced unstable separation due to the electrostatic repulsion between the electrophilic analytes and the negatively charged stationary phase. On-line concentration steps of step-gradient elution combined with anion selective injection (ASEI) were used to enhance the detection sensitivity of the CEC-MS method and all penicillin detection sensitivities were further improved (reduction in the limits of detection from 1.9–31 μg/L (normal injection mode) to 0.05–0.2 μg/L (on-line concentration mode)). Finally, this optimal on-line concentration CEC-MS method was applied to trace penicillin analyses in milk samples.
Keywords :
Charge monomer , Capillary electrochromatography-mass spectrometry , Polymeric monoliths , milk sample , penicillin
Journal title :
Talanta
Serial Year :
2012
Journal title :
Talanta
Record number :
1664194
Link To Document :
بازگشت