Micellar electrokinetic chromatography-electrospray ionization mass spectrometry for the identification of drug impurities

被引:19
作者
Mol, Roelof
Kragt, Else
Jimidar, Llias
de Jong, Gerhardus J.
Somsen, Govert W.
机构
[1] Univ Utrecht, Dept Biomed Anal, NL-3508 TB Utrecht, Netherlands
[2] Johnson & Johnson Pharmaceut R&D, Global Analyt Dept, B-2340 Beerse, Belgium
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2006年 / 843卷 / 02期
关键词
micellar electrokinetic chromatography (MEKC); mass spectrometry (MS); impurity profiling;
D O I
10.1016/j.jchromb.2006.06.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Previously, we have presented a system hyphenating continuous micellar electrokinetic chromatography (MEKC) with electrospray ionization mass spectrometry (ESI-MS). Here we evaluate this technique for its applicability in impurity profiling of drugs using galantamine and ipratropium as test samples. A background electrolyte (BGE) of 10 mM sodium phosphate (pH 7.5), 12.5-15% acetonitrile and 20 mm sodium dodecylsulfate (SDS) was used for the MEKC-MS analysis of a galantamine sample containing a number of related impurities, and a heat-treated solution of ipratropium containing a number of unknown degradation products. MEKC provided efficient separation of all sample constituents. Despite the presence of non-volatile BGEs, all impurities in the galantamine sample could be detected by ESI-MS in their respective extracted ion traces (XICs) with a detection sensitivity in the sub-mu g/ml range (full-scan mode). MS/MS detection provided useful product spectra allowing the structural characterization of the respective galantamine impurities. With the MEKC-MS/MS system, two degradation products could be revealed and identified in the heat-stressed ipratropium sample. The presented method shows good potential for the detection and structure elucidation of minor impurities in drug substances. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:283 / 288
页数:6
相关论文
共 18 条
[1]   Determination of drug-related impurities by capillary electrophoresis [J].
Altria, KD .
JOURNAL OF CHROMATOGRAPHY A, 1996, 735 (1-2) :43-56
[2]   Choice of capillary electrophoresis systems for the impurity profiling of drugs [J].
Hilhorst, MJ ;
Somsen, GW ;
de Jong, GJ .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 16 (07) :1251-1260
[3]  
Hilhorst MJ, 2001, ELECTROPHORESIS, V22, P1337
[4]   Pharmacology of bronchodilators used in the treatment of COPD [J].
Lötvall, J .
RESPIRATORY MEDICINE, 2000, 94 :S6-S10
[5]   Atmospheric pressure photoionization for enhanced compatibility in on-line micellar electrokinetic chromatography - Mass spectrometry [J].
Mol, R ;
de Jong, GJ ;
Somsen, GW .
ANALYTICAL CHEMISTRY, 2005, 77 (16) :5277-5282
[6]   Micellar electrokinetic chromatography: Current developments and future [J].
Molina, M ;
Silva, M .
ELECTROPHORESIS, 2002, 23 (22-23) :3907-3921
[7]   Recent advances in micellar electrokinetic chromatography [J].
Pappas, TJ ;
Gayton-Ely, M ;
Holland, LA .
ELECTROPHORESIS, 2005, 26 (4-5) :719-734
[8]   Micellar electrokinetic chromatography - From theoretical concepts to real samples (Review) [J].
Pyell, U .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2001, 371 (06) :691-703
[9]   Acetylcholinesterase inhibitors: novel activities of old molecules [J].
Racchi, M ;
Mazzucchelli, M ;
Porrello, E ;
Lanni, C ;
Govoni, S .
PHARMACOLOGICAL RESEARCH, 2004, 50 (04) :441-451
[10]  
Riekkola ML, 1997, PROCESS CONTR QUAL, V10, P169