Determination of malachite green and leucomalachite green in carp muscle by liquid chromatography with visible and fluorescence detection

• Published in: Journal of Chromatography A Vol. 1089; no. 1; pp. 187 - 192
• Main Authors: Mitrowska, Kamila, Posyniak, Andrzej, Zmudzki, Jan
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 30-09-2005; Elsevier
• Subjects: Analytical method; Aniline Compounds - analysis; Animals; Biological and medical sciences; Carp; Carps; Cyprinus carpio; drug residues; Fish and seafood industries; fluorescence; food analysis; food contamination; Food industries; Fundamental and applied biological sciences. Psychology; Leucomalachite green; liquid chromatography; Malachite green; metabolites; Muscles - chemistry; Reproducibility of Results; Residues; Rosaniline Dyes - analysis; Sensitivity and Specificity; skeletal muscle; Spectrometry, Fluorescence - methods; Residues; Leucomalachite green; Carp; Analytical method; Malachite green; Solid phase extraction; Edible fish; Chemical analysis; Metabolite; HPLC chromatography; Basic dye; Chemical enrichment; Tissue; Sample preparation; Muscle; Quantitative analysis; Trace analysis; Validation; Fluorescence detector; Pesticides; Triarylmethane dye; Visible spectrometry; Fish fillet; Contamination; Fungicide; Residue
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2005.07.004

A liquid chromatography-VIS/FLD method for the analysis of malachite green (MG) and its major metabolite, leucomalachite green (LMG) in carp muscle has been described. The method consists in an extraction with acetonitrile-buffer mixture followed by partioning with dichloromethane. Clean up and isolation were performed on SCX solid phase extraction (SPE) column. Chromatographic separation was achieved by using phenyl-hexyl column with an isocratic mobile phase consisting of acetonitrile and acetate buffer (0.05
M, pH 4.5) (60:40, v/v). Liquid chromatography with absorbance detector (
λ
=
620
nm) was used for the determination of MG while LMG was detected by fluorescence detector (
λ
ex
=
265
nm and
λ
em
=
360
nm). The both detectors were connected on-line which allowed direct analysis of a sample extract for MG and LMG without the need for any post-column procedure. The whole method has been validated, according to the EU requirements (Commission Decision 2002/657/EC). Specificity, stability, decision limit (CC
α), detection capability (CC
β), accuracy and precision were determined. Average recoveries of MG and LMG from muscle fortified at three levels (0.5, 1 and 2
μg/kg) were 62% (range from 60.4 to 63.5%) and 90% (range from 89.0 to 91.5%), respectively. Relative standard deviations (RSD) of recoveries at all fortification levels were less than 10.9 and 8.6% for MG and LMG, respectively. The calculated CC
α for MG and LMG were 0.15 and 0.13
μg/kg, and CC
β were 0.37 and 0.32
μg/kg, complying with the minimum required performance limit (MRPL) of 2
μg/kg (sum of MG and LMG).