Separation of lidocaine and its metabolites by capillary electrophoresis using volatile aqueous and nonaqueous electrolyte systems

The separation of the basic drug lidocaine and six of its metabolites has been investigated both by using volatile aqueous electrolyte system, at low pH and by employing non‐aqueous electrolyte systems. In aqueous systems, the best separation of the compounds under the investigated conditions was achieved by using the electrolyte 60 mM trifluoroacetic acid (TFA)/triethylamine (TEA) at pH 2.5 containing 15% methanol. With this electrolyte, all seven compounds were well separated with high efficiency and migration time repeatability. The separations with bare fused‐silica capillaries and polyacrylamide‐coated capillaries were compared with higher separation efficiency with the latter. On the other hand, near baseline separation of all the seven compounds was also obtained by employing the non‐aqueous electrolyte, 40 mM ammonium acetate in methanol and TFA (99:1, v/v), with comparable migration time repeatability but lower separation efficiency relative to the aqueous system.

[1]  M. Riekkola,et al.  Capillary zone electrophoresis of basic drugs in non-aqueous acetonitrile with buffers based on a conventional pH scale , 2001 .

[2]  M. Riekkola,et al.  Capillary zone electrophoresis of basic analytes in methanol as non-aqueous solvent mobility and ionisation constant. , 2001, Journal of chromatography. A.

[3]  M. Riekkola,et al.  Non-aqueous capillary electrophoresis. , 2000, Journal of chromatography. A.

[4]  T. Arvidsson,et al.  High-performance liquid chromatography-tandem electrospray mass spectrometry for the determination of lidocaine and its metabolites in human plasma and urine. , 2000, Journal of chromatography. B, Biomedical sciences and applications.

[5]  G. D. de Jong,et al.  Multiple solid-phase microextraction. , 2000, Journal of chromatography. A.

[6]  G. D. de Jong,et al.  Determination of lidocaine in plasma by direct solid-phase microextraction combined with gas chromatography. , 2000, Journal of chromatography. B, Biomedical sciences and applications.

[7]  T. Arvidsson,et al.  Evaluation of solid-phase microextraction in combination with gas chromatography (SPME-GC) as a tool for quantitative bioanalysis , 2000 .

[8]  R. A. Zeeuw,et al.  Coupling device for desorption of drugs from solid-phase extraction-pipette tips and on-line gas chromatographic analysis , 1999 .

[9]  A. Marzo,et al.  Highly sensitive bioassay of lidocaine in human plasma by high-performance liquid chromatography-tandem mass spectrometry. , 1999, Journal of chromatography. A.

[10]  M. Riekkola,et al.  Alcohols and wide‐bore capillaries in nonaqueous capillary electrophoresis , 1999, Electrophoresis.

[11]  P. Vouros,et al.  Peer Reviewed: Advances in CE/MS. , 1999 .

[12]  A. Cifuentes,et al.  Preparation of linear polyacrylamide-coated capillaries - Study of the polymerization process and its effect on capillary electrophoresis performance , 1999 .

[13]  L. Escuder-Gilabert,et al.  Analysis of pharmaceutical preparations containing local anesthetics by micellar liquid chromatography and spectrophotometric detection , 1999 .

[14]  H. Wan,et al.  Characterization of lidocaine and its metabolites in human plasma using capillary electrophoresis , 1999 .

[15]  H. Wätzig,et al.  Strategies for capillary electrophoresis: Method development and validation for pharmaceutical and biological applications , 1998, Electrophoresis.

[16]  S. Hansen,et al.  Nonaqueous capillary electrophoresis — its applicability in the analysis of food, pharmaceuticals and biological fluids , 1998, Electrophoresis.

[17]  T. Arvidsson,et al.  CHROMATOGRAPHIC BEHAVIOR OF UNDERIVATIZED LIDOCAINE AND METABOLITES IN CGC , 1998 .

[18]  S. Hansen,et al.  Separation of cationic cis-trans (Z-E) isomers and diastereoisomers using non-aqueous capillary electrophoresis , 1997 .

[19]  M. Riekkola,et al.  Selectivity in capillary electrophoresis in the presence of micelles, chiral selectors and non-aqueous media. , 1997, Journal of chromatography. A.

[20]  T. Yaksh,et al.  An improved method for the measurement of lidocaine and its metabolites in rat plasma. , 1997, Therapeutic drug monitoring.

[21]  J. Strong,et al.  Identification of 2,6-xylidine as a major lidocaine metabolite in human liver slices. , 1996, Drug metabolism and disposition: the biological fate of chemicals.

[22]  G. Clarke,et al.  Selectivity of capillary electrophoresis for the analysis of cardiovascular drugs , 1996 .

[23]  R. Cole,et al.  Analysis of tamoxifen and its metabolites by on-line capillary electrophoresis-electrospray ionization mass spectrometry employing nonaqueous media containing surfactants. , 1996, Analytical chemistry.

[24]  W. Hancock,et al.  Application of capillary electrophoresis, high-performance liquid chromatography, on-line electrospray mass spectrometry and matrix-assisted laser desorption ionization--time of flight mass spectrometry to the characterization of single-chain plasminogen activator. , 1995, Journal of chromatography. A.

[25]  G. Clarke,et al.  Investigation and optimisation of the use of organic modifiers in micellar electrokinetic chromatography , 1995 .

[26]  G. Strichartz Protracted relief of experimental neuropathic pain by systemic local anesthetics. How, where, and when. , 1995, Anesthesiology.

[27]  Stefan Fischer,et al.  Enhanced sensitivity for peptide mapping with electrospray liquid chromatography-mass spectrometry in the presence of signal suppression due to trifluoroacetic acid-containing mobile phases. , 1995, Journal of chromatography. A.

[28]  R. Becklin,et al.  The Amount of Ultraviolet Absorbance in a Synthetic Peptide is Directly Proportional to Its Number of Peptide Bonds , 1995 .

[29]  S. Terabe,et al.  Effect of organic modifier concentrations on electrokinetic migrations in micellar electrokinetic chromatography , 1995, Electrophoresis.

[30]  J. Bernal,et al.  Extraction of basic drugs from whole blood and determination by high performance liquid chromatography , 1994 .

[31]  R. Cole,et al.  Cetyltrimethylammonium chloride as a surfactant buffer additive for reversed-polarity capillary electrophoresis-electrospray mass spectrometry. , 1993, Journal of chromatography. A.

[32]  G. Chee,et al.  Reproducible and high-speed separation of basic drugs by capillary zone electrophoresis. , 1993, Journal of chromatography.

[33]  A. Scholer,et al.  Assessment of lidocaine metabolite formation in comparison with other quantitative liver function tests. , 1993, Journal of hepatology.

[34]  A. Camm,et al.  Relative efficacy and safety of intravenous drugs for termination of sustained ventricular tachycardia , 1990, The Lancet.

[35]  M. Björk,et al.  Capillary gas chromatographic method for the simultaneous determination of local anaesthetics in plasma samples. , 1990, Journal of chromatography.

[36]  M. Gray,et al.  High-performance liquid chromatography of lidocaine and nine of its metabolites in human plasma and urine. , 1987, Journal of chromatography.

[37]  A. Chen,et al.  Carrier-free zone electrophoresis, displacement electrophoresis and isoelectric focusing in a high-performance electrophoresis apparatus. , 1987, Journal of chromatography.

[38]  A. Wahlén,et al.  Lidocaine Base and Hydrochloride , 1985 .

[39]  Stellan Hjertén,et al.  High-performance electrophoresis : Elimination of electroendosmosis and solute adsorption , 1985 .

[40]  K. Oka,et al.  Simultaneous determination of lidocaine and its principal metabolites by liquid chromatography on silica gel, with aqueous eluent. , 1984, Clinical chemistry.

[41]  T. Wenger,et al.  Simultaneous determination of lidocaine and its metabolites in plasma and myocardium. , 1984, Journal of chromatography.

[42]  N. Carliner,et al.  Lidocaine and its active metabolites , 1978, Clinical pharmacology and therapeutics.