Simultaneous Determination of Indole-3-Acetic Acid and Indole-3-Butyric Acid in Plant by Field-Amplified Sample Stacking Open-Tubular Capillary Electrochromatography Based on Solid-Phase Extraction with Calixarene Sorbent

被引:12
作者
Yang, Liu [1 ]
Chen, Yanlong [1 ]
Zhao, Shengnan [1 ]
Zhang, Wenfen [1 ]
Du, Huifang [1 ]
Deng, Zhifen [1 ]
Zhang, Shusheng [1 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, Kexue Rd 100, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Indole-3-acetic acid; Beta-indolebutyric acid; Open-tubular capillary electrochromatography; Methyldiethanolamine amination polychloromethyl styrene; SPE; TANDEM MASS-SPECTROMETRY; PERFORMANCE LIQUID-CHROMATOGRAPHY; ABSCISIC-ACID; ZONE-ELECTROPHORESIS; GAS-CHROMATOGRAPHY; STATIONARY-PHASE; INORGANIC ANIONS; BONDED SILICA; MS/MS METHOD; PHYTOHORMONES;
D O I
10.1007/s10337-015-2999-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes the preparation and application of methyldiethanolamine amination polychloromethyl styrene nanolatex (MDEAPL) and MDEAPL coated capillary column (ccc-MDEAPL). The ccc-MDEAPL column was characterized with steady EOF values from -14.6 x 10(-5) to -19.8 x 10(-5) at pH 7.08-7.56. A method using tetraazacalix[2]arene[2]triazine-modified silica gel (NCS) as solid-phase extraction (SPE) sorbent was developed for concentrating and purifying the two phytohormones, indole-3-acetic acid (IAA) and beta-indolebutyric acid (IBA) of different plants. The determination conditions of IAA and IBA for field-amplified sample stacking open-tubular capillary electrochromatography based on SPE with NCS sorbent (NCS-SPE-FASS-OT-CEC) were optimized as follows: background electrolyte, 30 mmol L-1 Tris + 24 mmol L-1 HClO4 (30 % acetonitrile, pH 7.24); ccc-MDEAPL, 50 mu m i.d. x 50 cm (effective length 41.5 cm); separation voltage, -25 kV; column temperature, 25 degrees C; UV detection wavelength, 230 nm; water-plug injection, 30 mbar x 20 s; sample electrokinetic injection, -20 kV x 20 s. Under the optimized conditions, IAA and IBA were well separated within 6 min (Rs > 1.5). The NCS-SPE-FASS-OT-CEC method was validated in terms of linearity, sensitivity, selectivity, precision and accuracy. The detection limits were 8 ng mL(-1) for IAA and 25 ng mL(-1) for IBA (S/N = 3), respectively. The overall recoveries ranged from 81.0 to 89.0 %. The developed method was successfully applied for the determination of IAA and IBA in different positions of various plants.
引用
收藏
页码:243 / 254
页数:12
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