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Merck
  • Multi-residue determination of 115 veterinary drugs and pharmaceutical residues in milk powder, butter, fish tissue and eggs using liquid chromatography-tandem mass spectrometry.

Multi-residue determination of 115 veterinary drugs and pharmaceutical residues in milk powder, butter, fish tissue and eggs using liquid chromatography-tandem mass spectrometry.

Analytica chimica acta (2015-06-21)
Marilena E Dasenaki, Nikolaos S Thomaidis
要旨

A simple and sensitive multi-residue method for the determination of 115 veterinary drugs and pharmaceuticals, belonging in more than 20 different classes, in butter, milk powder, egg and fish tissue has been developed. The method involves a simple generic solid-liquid extraction step (solvent extraction, SE) with 0.1% formic acid in aqueous solution of EDTA 0.1% (w/v)-acetonitrile (ACN)-methanol (MeOH) (1:1:1, v/v) with additional ultrasonic-assisted extraction. Precipitation of lipids and proteins was promoted by subjecting the extracts at very low temperature (-23°C) for 12h. Further cleanup with hexane ensures fat removal from the matrix. Analysis was performed by liquid chromatography coupled with electrospray ionization and tandem mass spectrometry (LC-ESI-MS/MS). Two separate runs were performed for positive and negative ionization in multiple reaction monitoring mode (MRM). Particular attention was devoted to extraction optimization: different sample-to-extracting volume ratios, different concentrations of formic acid in the extraction solvent and different ultrasonic extraction temperatures were tested in butter, egg and milk powder samples. The method was also applied in fish tissue samples. It was validated, on the basis of international guidelines, for all four matrices. Quantitative analysis was performed by means of standard addition calibration. For over 80% of the analytes, the recoveries were between 50% and 120% in all matrices studied, with RSD values in the range of 1-18%. Limits of detection (LODs) and quantification (LOQs) ranged from 0.008 μg kg(-1) (oxfendazole in butter) to 3.15 μg kg(-1) (hydrochlorthiazide in egg). The evaluated method provides reliable screening, quantification, and identification of 115 veterinary drug and pharmaceutical residues in foods of animal origin and has been successfully applied in real samples.

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製品内容

Sigma-Aldrich
ギ酸アンモニウム, ≥99.995% trace metals basis
Sigma-Aldrich
ギ酸アンモニウム 溶液, BioUltra, 10 M in H2O
Sigma-Aldrich
メタノール, JIS special grade, ≥99.8%
Sigma-Aldrich
アセトニトリル, anhydrous, 99.8%
Sigma-Aldrich
メタノール, SAJ first grade, ≥99.5%
Sigma-Aldrich
メタノール, anhydrous, 99.8%
Sigma-Aldrich
ギ酸, ≥95%, FCC, FG
Supelco
ギ酸アンモニウム 溶液, 10 mM in H2O, suitable for HPLC
Sigma-Aldrich
ヘキサン, JIS special grade, ≥96.0%
Sigma-Aldrich
ヘキサン, anhydrous, 95%
Sigma-Aldrich
アセトニトリル, electronic grade, 99.999% trace metals basis
Sigma-Aldrich
メタノール, suitable for HPLC
Sigma-Aldrich
ギ酸, JIS special grade, ≥98.0%
Sigma-Aldrich
アセトニトリル, ≥99.8%, suitable for HPLC
Sigma-Aldrich
メタノール, SAJ special grade
Sigma-Aldrich
ヘキサン, SAJ first grade, ≥95.0%
Sigma-Aldrich
アセトニトリル, ≥99.8%, for residue analysis, JIS 300
Sigma-Aldrich
ヘキサン, suitable for HPLC
Sigma-Aldrich
メタノール, NMR reference standard
Sigma-Aldrich
アセトニトリル, JIS special grade, ≥99.5%
Sigma-Aldrich
ヘキサン, JIS 300, ≥96.0%, for residue analysis
Sigma-Aldrich
ヘキサン, for residue analysis, JIS 5000
Sigma-Aldrich
Methanol-12C, 99.95 atom % 12C
Sigma-Aldrich
ヘキサン, JIS 1000, ≥96.0%, for residue analysis
Sigma-Aldrich
ギ酸, SAJ first grade, 88.0-89.5%
Sigma-Aldrich
アセトニトリル, ≥99.5%, ACS reagent
Sigma-Aldrich
アセトニトリル 溶液, contains 0.1 % (v/v) trifluoroacetic acid, suitable for HPLC
Supelco
メタノール 溶液, contains 0.10 % (v/v) formic acid, UHPLC, suitable for mass spectrometry (MS), ≥99.5%
Sigma-Aldrich
メタノール, JIS 300, ≥99.8%, for residue analysis
Sigma-Aldrich
アセトニトリル 溶液, contains 0.1 % (v/v) formic acid, suitable for HPLC