OPTIMUM CONDITIONS FOR PREPARATIVE OPERATION OF CAPILLARY ZONE ELECTROPHORESIS

被引:26
作者
CIFUENTES, A [1 ]
XU, X [1 ]
KOK, WT [1 ]
POPPE, H [1 ]
机构
[1] UNIV AMSTERDAM,AMSTERDAM INST MOLEC STUDIES,ANALYT CHEM LAB,1018 WV AMSTERDAM,NETHERLANDS
关键词
D O I
10.1016/0021-9673(95)00539-Y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The possibilities to use capillary zone electrophoresis (CZE) as a preparative tool have been studied, mostly from a theoretical point of view. The preparative performance of CZE is quantitated by the production rate, the amount of analyte that can be purified per unit of time. The production rate available with CZE is shown to depend in the first place on the chemical characteristics of the analyte-buffer combination. A figure of merit can be defined for a buffer system, describing its susceptibility to analyte overloading. Methods to find an optimal buffer system are referred to. It is shown that the loadability of the system is inversely proportional to the plate number required for the separation. A second important factor for the maximum production rate is shown to be the thermal management of the instrumental system, The average increase of the solution temperature and the non-uniform migration velocity by temperature differences within the solutions are discussed. It is shown that in practical cases the temperature rise of the solutions will be the main limiting factor when high fields are used. With low fields, which in general give a higher production rate, siphoning of the solution becomes the dominant limitation for the production rate. With cylindrical capillaries the highest production rate that can be obtained under practical conditions is in the order of 5 . 10(-13) mol s(-1). Experimental and theoretical results indicate that with rectangular capillaries the production rate can be increased by a factor of three.
引用
收藏
页码:141 / 156
页数:16
相关论文
共 35 条
[1]   PEAK HOMOGENEITY DETERMINATION AND MICROPREPARATIVE FRACTION COLLECTION BY CAPILLARY ELECTROPHORESIS FOR PHARMACEUTICAL ANALYSIS [J].
ALTRIA, KD ;
DAVE, YK .
JOURNAL OF CHROMATOGRAPHY, 1993, 633 (1-2) :221-225
[2]   ON THE DISPERSION OF A SOLUTE BY DIFFUSION, CONVECTION AND EXCHANGE BETWEEN PHASES [J].
ARIS, R .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1959, 252 (1271) :538-550
[3]   CALCULATION OF THE COMPOSITION OF SAMPLE ZONES IN CAPILLARY ZONE ELECTROPHORESIS .1. MATHEMATICAL-MODEL [J].
BECKERS, JL .
JOURNAL OF CHROMATOGRAPHY A, 1995, 693 (02) :347-357
[4]   ELECTRICALLY DRIVEN OPEN-TUBULAR LIQUID-CHROMATOGRAPHY [J].
BRUIN, GJM ;
TOCK, PPH ;
KRAAK, JC ;
POPPE, H .
JOURNAL OF CHROMATOGRAPHY, 1990, 517 :557-572
[5]   RECTANGULAR CAPILLARY ELECTROPHORESIS - SOME THEORETICAL CONSIDERATIONS [J].
CIFUENTES, A ;
POPPE, H .
CHROMATOGRAPHIA, 1994, 39 (7-8) :391-404
[6]  
CIFUENTES A, IN PRESS ELECTROPHOR
[7]   CONTRIBUTION TO CHOICE OF OPTIMAL GEOMETRIC CONDITIONS FOR PREPARATIVE LIQUID-CHROMATOGRAPHY [J].
DEJONG, AWJ ;
POPPE, H ;
KRAAK, JC .
JOURNAL OF CHROMATOGRAPHY, 1978, 148 (01) :127-141
[8]   COMPUTER-SIMULATION FOR CAPILLARY ZONE ELECTROPHORESIS - A QUANTITATIVE APPROACH [J].
ERMAKOV, SV ;
RIGHETTI, PG .
JOURNAL OF CHROMATOGRAPHY A, 1994, 667 (1-2) :257-270
[9]   EXPERIMENTAL AND THEORETICAL-STUDY OF ARTIFACTUAL PEAK SPLITTING IN CAPILLARY ELECTROPHORESIS [J].
ERMAKOV, SV ;
ZHUKOV, MY ;
CAPELLI, L ;
RIGHETTI, PG .
ANALYTICAL CHEMISTRY, 1994, 66 (22) :4034-4042
[10]   INDIRECT PHOTOMETRIC DETECTION IN CAPILLARY ZONE ELECTROPHORESIS [J].
FORET, F ;
FANALI, S ;
OSSICINI, L ;
BOCEK, P .
JOURNAL OF CHROMATOGRAPHY, 1989, 470 (01) :299-308