Identification of lidocaine and its metabolites in post-adminstration equine urine by ELISA and MS/MS

Citation
L. Dirikolu et al., Identification of lidocaine and its metabolites in post-adminstration equine urine by ELISA and MS/MS, J VET PHARM, 23(4), 2000, pp. 215-222
Citations number
9
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS
ISSN journal
01407783 → ACNP
Volume
23
Issue
4
Year of publication
2000
Pages
215 - 222
Database
ISI
SICI code
0140-7783(200008)23:4<215:IOLAIM>2.0.ZU;2-P
Abstract
Lidocaine is a local anesthetic drug that is widely used in equine medicine . It has the advantage of giving good local anesthesia and a longer duratio n of action than procaine. Charles C. Thomas, Springfield, IL). Although ap proved for use in horses in training by the American Association of Equine Practitioners (AAEP), lidocaine is also an Association of Racing Commission ers International (ARCI) Class 2 drug and its detection in forensic samples can result in significant penalties. Lidocaine was observed as a monoprotonated ion at m/z 235 by ESI+ MS/MS (el ectrospray ionization-positive ion mode) analysis. The base peak ion at m/z 86, representing the postulated methylenediethylamino fragment [CH2N(CH2CH 3)(2)](+), was characteristic of lidocaine and 3-hydroxylidocaine in both E SI+ and EI (electron impact- positive ion mode) mass spectrometry. In addit ion, we identified an ion at m/z 427 as the principal parent ion of the ion at m/z 86, consistent with the presence of a protonated analog of 3-hydrox ylidocaine-glucuronide. We also sought to establish post-administration ELISA-based 'detection time s' for lidocaine and lidocaine-related compounds in urine following single subcutaneous injections of various doses (10, 40, 400 mg). Our findings sug gest relatively long ELISA based 'detection times' for lidocaine following higher doses of this drug.