Surfactant-bound monolithic columns for CEC

被引:8
作者
Gu, Congying [1 ,2 ]
He, Jun [1 ]
Jia, Jinping [2 ]
Fang, Nenghu [2 ]
Shamsi, Shahab A. [1 ]
机构
[1] Georgia State Univ, Dept Chem, Ctr Biotechnol & Drug Design, Atlanta, GA 30303 USA
[2] Shanghai Jiao Tong Univ, Dept Environm Sci & Engn, Shanghai 200030, Peoples R China
基金
美国国家卫生研究院;
关键词
11-Acrylaminoundecanoic acid (AAUA) monomer; D-Optimal design; Mixed-mode stationary phase; Pesticides and isomer separation; Physical and chromatographic properties; PERFORMANCE LIQUID-CHROMATOGRAPHY; CAPILLARY ELECTROCHROMATOGRAPHY; STATIONARY PHASES; EXPERIMENTAL-DESIGN; POLYMER MONOLITHS; MASS-SPECTROMETRY; POROUS PROPERTIES; SEPARATION MEDIA; NUCLEIC-ACIDS; OPTIMIZATION;
D O I
10.1002/elps.200900434
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
A novel anionic surfactant bound monolithic stationary phase based on 11-acrylaminoundecanoic acid is designed for CEC. The monolith possessing bonded undecanoyl groups (hydrophobic sites) and carboxyl groups (weak cationic ion-exchange sites) were evaluated as a mixed-mode stationary phase in CEC for the separation of neutral and polar solutes. Using a multivariate D-optimal design the composition of the polymerization mixture was modeled and optimized with five alkylbenzenes and seven alkyl phenyl ketones as test solutes. The D-optimal design indicates a strong dependence of electrochromatographic parameters on the concentration of 11-acrylaminoundecanoic acid monomer and porogen (water) in the polymerization mixture. A difference of 6, 8 and 13% RSD between the predicted and the experimental values in terms of efficiency, resolution and retention time, respectively, indeed confirmed that the proposed approach is practical. The physical (i.e. morphology, porosity and permeability) and chromatographic properties of the monolithic columns were thoroughly investigated. With the optimized monolithic column, high efficiency separation of N-methylcarbamates pesticides and positional isomers was successfully achieved. It appears that this type of mixed-mode monolith (containing both chargeable and hydrophobic sites) may have a great potential as a new generation of CEC stationary phase.
引用
收藏
页码:3814 / 3827
页数:14
相关论文
共 54 条
[1]
ANDERSON MJ, 2002, RUBBER PLASTIC 1021
[2]
[Anonymous], 2005, PRACTICAL HIGH PERFO
[3]
Development of a liquid-liquid extraction procedure for five 1,4-dihydropyridines calcium channel antagonists from human plasma using experimental design [J].
Baranda, AB ;
Etexbarria, N ;
Jiménez, RM ;
Alonso, RM .
TALANTA, 2005, 67 (05) :933-941
[4]
Development of acrylate-based monolithic stationary phases for electrochromatographic separations [J].
Barrioulet, MP ;
Delaunay-Bertoncini, N ;
Demesmay, C ;
Rocca, JL .
ELECTROPHORESIS, 2005, 26 (21) :4104-4115
[5]
Convective Interaction Media short monolithic columns: Enabling chromatographic supports for the separation and purification of large biomolecules [J].
Barut, M ;
Podgornik, A ;
Brne, P ;
Strancar, A .
JOURNAL OF SEPARATION SCIENCE, 2005, 28 (15) :1876-1892
[6]
Capillary electrochromatography with monolithic stationary phases - II. Preparation of cationic stearyl-acrylate monoliths and their electrochromatographic characterization [J].
Bedair, M ;
El Rassi, Z .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1013 (1-2) :35-45
[7]
Multiple response optimization applied to the development of a capillary electrophoretic method for pharmaceutical analysis [J].
Candioti, LV ;
Robles, JC ;
Mantovani, VE ;
Goicoechea, HC .
TALANTA, 2006, 69 (01) :140-147
[8]
Supercritical carbon dioxide extraction of turmeric oil from Curcuma longa Linn and purification of turmerones [J].
Chang, LH ;
Jong, TT ;
Huang, HS ;
Nien, YF ;
Chang, CMJ .
SEPARATION AND PURIFICATION TECHNOLOGY, 2006, 47 (03) :119-125
[9]
Application of statistical experimental design for optimization of alkaline protease production from Bacillus sp RGR-14 [J].
Chauhan, B ;
Gupta, R .
PROCESS BIOCHEMISTRY, 2004, 39 (12) :2115-2122
[10]
Fritless capillary columns for HPLC and CEC prepared by immobilizing the stationary phase in an organic polymer matrix [J].
Chirica, GS ;
Remcho, VT .
ANALYTICAL CHEMISTRY, 2000, 72 (15) :3605-3610