Determination of lidocaine and its two N-desethylated metabolites in dog and horse plasma by high-performance liquid chromatography combined with electrospray ionization tandem mass spectrometry

A sensitive method for the quantification of lidocaine and its metabolites, monoethylglycinexylidide (MEGX) and glycinexylidide (GX), in animal plasma using high-performance liquid chromatography combined with electrospray ionization mass spectrometry is described. The sample preparation includes a liquid–liquid extraction with methyl tert-butylmethyl ether after addition of 2 M sodium hydroxide. Ethylmethylglycinexylidide (EMGX) is used as an internal standard. For chromatographic separation, an ODS Hypersil column was used. Isocratic elution was achieved with 0.01 M ammonium acetate and acetonitrile as mobile phases. Good linearity was observed in the range of 2.5–1000 ng ml−1 for lidocaine in both dog and horse plasma. For MEGX, linear calibration curves were obtained in the range of 5–1000 ng ml−1 and 20–1000 ng ml−1 for dog and horse plasma, respectively. In dog and horse plasma good linearity was observed in the range of 200–1500 ng ml−1 for GX. The limit of quantification (LOQ) in dog plasma for lidocaine, MEGX and GX was set at 2.5 ng ml−1, 20 ng ml−1 and 200 ng ml−1, respectively. For horse plasma a limit of quantification of 2.5 ng ml−1, 5 ng ml−1 and 200 ng ml−1 was achieved for lidocaine, MEGX and GX, respectively. In dog plasma, the limit of detection (LOD) was found to be 0.8 ng ml−1, 2.3 ng ml−1 and 55 ng ml−1 for lidocaine, MEGX and GX, respectively. In horse plasma the LODʹs found for lidocaine, MEGX and GX, were 1.1 ng ml−1, 0.5 ng ml−1 and 13 ng ml−1, respectively. The method was shown to be of use in pharmacokinetic studies after application of a transdermal patch in dogs and after an intravenous infusion in horses.