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Preparation of organic-inorganic hybrid silica monolith with octyl and sulfonic acid groups for capillary electrochromatograhpy and application in determination of theophylline and caffeine in beverage
被引:45
|作者:
Chen, Ming-Luan
[1
]
Zheng, Ming-Ming
[1
]
Feng, Yu-Qi
[1
]
机构:
[1] Wuhan Univ, Dept Chem, Minist Educ, Key Lab Analyt Chem Biol & Med, Wuhan 430072, Peoples R China
关键词:
Capillary electrochromatograhpy;
Organic-inorganic hybrid silica monolith;
Caffeine and theophylline;
Beverage;
PERFORMANCE LIQUID-CHROMATOGRAPHY;
SOLID-PHASE MICROEXTRACTION;
STATIONARY PHASES;
MIXED-MODE;
MASS-SPECTROMETRY;
REVERSED-PHASE;
ZONE-ELECTROPHORESIS;
ELECTROOSMOTIC FLOW;
GAS CHROMATOGRAPHY;
COLUMN;
D O I:
10.1016/j.chroma.2010.03.032
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
An organic-inorganic hybrid silica monolithic column with octyl and sulfonic acid groups has been prepared by sol-gel technique for capillary electrochromatograhpy. The structure of hybrid monolith was optimized by changing the composition of tetraethoxysilane (TEOS), octyltriethoxysilane (C-8-TEOS) and 3-mercaptopropyltrimethoxysilane (MPTMS) in the mixture of precursors. Then, the obtained hybrid monolith was oxidized using hydrogen peroxide (30%, w/w) to yield sulfonic acid groups. The sulfonic acid group, which served as strong cation-exchanger, dominated the charge on the surface of the capillary column and generated stable electroosmotic flow (EOF) in a wide range of pH. The monolithic column was characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy and elemental analysis (EA), and the performance of column was evaluated in detail by separating different kinds of compounds with column efficiency up to 155,000 plates/m for thiourea. In addition, this monolithic column was also applied in the analysis of theophylline (TP) and caffeine (CA) in beverages. The detection limits were 0.39 and 0.48 mu g/mL for theophylline and caffeine, respectively. The method reproducibility was tested by evaluating the intra- and inter-clay precisions, and relative standard deviations of less than 3.9 and 8.4%. respectively, were obtained. Recoveries of compounds from spiked beverage samples ranged from 87.2 to 105.2%. (C) 2010 Elsevier B.V. All rights reserved.
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页码:3547 / 3556
页数:10
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