Determination of Gentian Violet, Its Demethylated Metabolites, and Leucogentian Violet in Chicken Tissue by Liquid Chromatography with Electrochemical Detection

Abstract

Abstract A method Is presented for determination of residues of gentian violet (GV), Its demethylated metabolites (pentamethyl and tetramethyl), and leucogentian violet (LGV) In chicken tissue. The analytes are extracted from tissue with acetonitrlle/ buffer and partitioned Into methylene chloride. Polar lipids are removed on an alumina column followed by partitioning Into methylene chloride from a citrate buffer. The compounds of interest are isolated on a disposable carboxyl- Ic acid cation exchange column and then eluted with 0.02% HCI In methanol. GV, Its metabolites, and LGV are determined by liquid chromatography using Isocratlc elution with a buffered mobile phase from a cyano column and amperometrlc electrochemical detection at +1.000 V. Average recoveries of GV and LGV from commercially purchased chicken liver fortified with 20 ppb of each compound were 92% [standard deviation (SD) = 7, coefficient of variation (CV) = 7.6%] and 86% (SD = 7, CV = 8.1 %), respectively. Average recoveries of GV, LGV, the pentamethyl metabolite, and 1 of the tetramethyl metabolites from control chicken liver (provided by the Center for Veterinary Medicine) fortified with 20 ppb of each compound were 80% (SD = 7, CV = 8.8%), 76% (SD = 3, CV = 3.9%), 83% (SD = 6, CV = 7.2%), and 76% (SD = 8, CV = 10.5%), respectively. Mean results from 10 analyses of residue-Incurred chicken liver were 31 ppb GV (SD = 3, CV = 9.7%), 34 ppb pentamethyl metabolite (SD = 3, CV = 8.8%), and 40 ppb tetramethyl metabollte(s) (SD = 2, CV = 5.0%), for an average value of 105 ppb total residues (SD = 6, CV = 5.7%); no LGV was found. Data are also presented to show applicability of the method to muscle tissue.