Internal Standard Capillary Electrophoresis as a High-Throughput Method for pKa Determination in Drug Discovery and Development

被引:21
作者
Cabot, Joan M.
Fuguet, Elisabet
Roses, Marti [1 ]
机构
[1] Univ Barcelona, Dept Quim Analit, E-08028 Barcelona, Spain
关键词
acidity constant; IS-CE; high-throughput method; pKa determination; internal standard; capillary electrophoresis; ACIDITY CONSTANTS; DISSOCIATION-CONSTANTS; ZONE-ELECTROPHORESIS; VALUES; SOLUBILITY; MOBILITY; WATER;
D O I
10.1021/co500059p
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel high-throughput method for determining acidity constants (pK(a)) by capillary electrophoresis (CE) is developed. The method, based on the use of an internal standard (IS-CE), is implemented as a routine method for accurate experimental pKa determination of drugs undergoing physicochemical measurements in drug discovery laboratories. Just two electropherograms at 2 different pH values are needed to calculate an acidity constant. Several ISs can be used in the same buffer and run to enhance precision. With 3 ISs, for example, the pK(a) of the test compound (TC) can be obtained in triplicate in less than 3 min of electrophoresis. It has been demonstrated that the IS-CE method eliminates some systematic errors, maintaining, or even increasing the precision of the results compared with other methods. Furthermore, pH buffer instability during electrophoretic runs is not a problem in the IS-CE method. It is also proved that after 16 h of electroseparation using the same buffer vial, pH may change by around one unit; but the pK(a) calculated by the IS-CE method remains constant. Thus, IS-CE is a powerful high-throughput method for pKa determination in drug discovery and development.
引用
收藏
页码:518 / 525
页数:8
相关论文
共 32 条
[1]   A comparative study of capillary zone electrophoresis and pH-potentiometry for determination of dissociation constants [J].
Andrasi, Melinda ;
Buglyo, Peter ;
Zekany, Laszlo ;
Gaspar, Attila .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2007, 44 (05) :1040-1047
[2]  
Avdeef Alex, 2001, Current Topics in Medicinal Chemistry, V1, P277, DOI 10.2174/1568026013395100
[3]   Determination of pKa values of active pharmaceutical ingredients [J].
Babic, Sandra ;
Horvat, Alka J. M. ;
Pavlovic, Dragana Mutavdzic ;
Kastelan-Macan, Marija .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2007, 26 (11) :1043-1061
[4]   Comparison between capillary electrophoresis, liquid chromatography, potentiometric and spectrophotometric techniques for evaluation of pKa values of zwitterionic drugs in acetonitrile-water mixtures [J].
Barbosa, J ;
Barrón, D ;
Jiménez-Lozano, E ;
Sanz-Nebot, V .
ANALYTICA CHIMICA ACTA, 2001, 437 (02) :309-321
[5]  
Barry B.W., 2001, EUR J PHARM SCI, V14, P101
[6]   The preparation of background electrolytes capillary zone electrophoresis: Golden rules and pitfalls [J].
Beckers, JL ;
Bocek, P .
ELECTROPHORESIS, 2003, 24 (03) :518-535
[7]   High-throughput measurement of pKa values in a mixed-buffer linear pH gradient system [J].
Box, K ;
Bevan, C ;
Comer, J ;
Hill, A ;
Allen, R ;
Reynolds, D .
ANALYTICAL CHEMISTRY, 2003, 75 (04) :883-892
[8]   Using Measured pKa, LogP and Solubility to Investigate Supersaturation and Predict BCS Class [J].
Box, K. J. ;
Comer, J. E. A. .
CURRENT DRUG METABOLISM, 2008, 9 (09) :869-878
[9]   AUTOMATED PK(A) DETERMINATION AT LOW SOLUTE CONCENTRATIONS BY CAPILLARY ELECTROPHORESIS [J].
CLEVELAND, JA ;
BENKO, MH ;
GLUCK, SJ ;
WALBROEHL, YM .
JOURNAL OF CHROMATOGRAPHY A, 1993, 652 (02) :301-308
[10]  
Comer W. T., 2013, REF MODULE CHEM MOL, DOI [10.1016/B978-0-12-409547-2.02699-8, DOI 10.1016/B978-0-12-409547-2.02699-8]