Veterinary Drug Detection in Pork and Milk

Similar documents
Determination, Confirmation and Quantitation of Multi-Class Antibiotic Residues in Milk by UHPLC MS/MS

Determination of Benzimidazole Residues in Animal Tissue by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry

Ultra-Fast Analysis of Contaminant Residue from Propolis by LC/MS/MS Using SPE

Rapid LC-MS/MS Method for the Analysis of Fipronil and Amitraz Insecticides and Associated Metabolites in Egg and Other Poultry Products

Quantification of Chloramphenicol in Chicken Using Xevo TQD with RADAR Technology

Sensitive and selective analysis of fipronil residues in eggs using Thermo Scientific GC-MS/MS triple quadrupole technology

Screening 36 Veterinary Drugs in Animal Origin Food by LC/MS/MS Combined with Modified QuEChERS Method

Multi-residue Screening of Veterinary Drugs (I) and (II) in Meat According to the Japan Positive List Using Cartridge-based SPE and LC-MS/MS

Analysis of Multiclass Veterinary Drugs in Baby Food by Ultra Fast Chromatography with High Performance Triple Quadrupole Mass Spectrometry

Extraction and Cleanup Protocols for LC-MS/MS Multiresidue Determination of Veterinary Drugs in Tissue and Milk Samples

Multi-residue Method II for Veterinary Drugs by HPLC (Animal and Fishery Products)

[ APPLICATION NOTE ] Analysis of Ketamine and Xylazine in Rat Tissues Using the ACQUITY UPLC with 2D Technology APPLICATION BENEFITS INTRODUCTION

Quantification of Several Acidic Drugs in Equine Serum Using LC MS-MS

A Unique Approach to Managing the Problem of Antibiotic Resistance

Automated Online Multi-Residue LC-MS/MS Method for the Determination of Antibiotics in Chicken Meat

International Journal of Pharmacy and Pharmaceutical Sciences. Research Article

Stability of Tylosin in Honey Impact on Residue Analysis Don Noot, Tom Thompson

One Analysis, One Column, Less than 9 Minutes for Over 60 Multiclass Antibiotics

An LC-MS/MS method to determine antibiotic residues in distillers grains

Detection of residues of quinolones in milk

Multi-residue Determination of Polar Veterinary Drugs in Livestock and Fishery Products by Liquid Chromatography/ Tandem Mass Spectrometry

ANTIBIOTICS IN PLASMA

Multi-residue Automated Turbulent Flow Online LC-MS/MS Method for the Determination of Antibiotics in Milk

ANTIBIOTICS RESIDUES IN HONEY: VALIDATION PROCEDURE HONEY ANALYTICAL METHODS VALIDATION

Oasis PRiME HLB Food Applications Notebook

Compliance. Should you have any questions, please contact Praveen Pabba, Ph.D., ( or

Pharma Research Library. 2013, Vol. 1(1):19-29

Fluoroquinolones ELISA KIT

Available online at

Quantitative and confirmatory analysis of veterinary drug residues in food of animal origin by UPLC- MS/MS after QuEChERS clean-up

Determination of Acaricides in Korean Honey Bull. Korean Chem. Soc. 2008, Vol. 29, No

Streptomycin Sulfate According to USP

C 22 H 28 FNa 2 O 8 Pıı516.4

DETERMINATION OF ACTIVE SUBSTANCES IN MULTICOMPONENT VETERINARY PREPARATIONS OF ANTIPARASITIC ACTION BY HPLC METHOD

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE SIMULTANEOUS ESTIMATION OF ALISKIREN AND AMLODIPINE IN TABLET DOSAGE FORM

Accepted Manuscript. Authors: Meritxell Gros, Sara Rodríguez-Mozaz, Damià Barceló

Analysis of Veterinary Drugs in Meat with the Agilent 6495 Triple Quadrupole LC/MS

IJCBS, 10(2016): International Journal of Chemical and Biochemical Sciences (ISSN )

Multilaboratory Trial for Determination of Ceftiofur Residues in Bovine and Swine Kidney and Muscle, and Bovine Milk

Determination of gentamicin and related impurities in gentamicin sulfate

ABSTRACT. Usharani N, Divya K and Ashrtiha VVS. Original Article

European Public MRL assessment report (EPMAR)

Development and Validation of RP-HPLC Method for Determination of Related Substances of Medetomidine in Bulk Drug

Ensuring Customer Success

Journal of Integrative Agriculture 2018, 17(6): Available online at ScienceDirect

Analysis of Hormones & Anabolics

COMMITTEE FOR VETERINARY MEDICINAL PRODUCTS

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF AMLODIPINE BESYLATE AND IRBESARTAN

Multi-residue Method I for Veterinary Drugs by HPLC (Animal and Fishery Products)

Determination of ofloxacin in bulk drug and pharmaceutical dosage form by high performance liquid chromatography method

Should you have any questions, please contact Edith Chang, Ph.D., Senior Scientific Liaison ( or

Quantification of EPA 1694 Pharmaceuticals and Personal Care Products in Water at the ng/l Level Utilizing Online Sample Preparation with LC-MS/MS

Journal of Applied Pharmaceutical Research ISSN No

COMMITTEE FOR VETERINARY MEDICINAL PRODUCTS

Simultaneous Determination of Danofloxacin and Difloxacin Residues in Poultry Meat using High Pressure Liquid Chromatography with PDA Detection

Occurrence of Antibiotics in Drinking Water

Journal of Global Trends in Pharmaceutical Sciences

AMOXICILLIN AND CLAVULANIC ACID TABLETS Draft proposal for The International Pharmacopoeia (February 2018)

Development and validation of a HPLC analytical assay method for amlodipine besylate tablets: A Potent Ca +2 channel blocker

SPECTROPHOTOMETRIC ESTIMATION OF MELOXICAM IN BULK AND ITS PHARMACEUTICAL FORMULATIONS

Using Charm II 7600 For Residue Testing in Meats in Barbados

Oasis PRiME HLB - Introducing A New Sorbent for the Sample Cleanup of Food Matrices

The mission of the U.S. Department of Agriculture

Analytica Chimica Acta 529 (2005)

International Journal of Pharmaceutical Research & Analysis

PO. Vasan, Gandhinagar District, Gujarat, India, 3 Dean at Faculty of Pharmacy, Dharmsinh Desai University, Nadiad, Gujarat, India.

VALIDATED RP-HPLC METHOD FOR THE SIMULTANEOUS DETERMINATION OF AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM IN BULK AND PHARMACEUTICAL FORMULATION

COMMITTEE FOR MEDICINAL PRODUCTS FOR VETERINARY USE

Application of Peristaltic Filling for Flexibility and Accuracy

Development and Validation of Amlodipine Impurities in Amlodipine Tablets Using Design Space Computer Modeling

European public MRL assessment report (EPMAR)

Development and validation of HPLC method for simultaneous estimation of Amlodipine besylate and Enalapril maleate in solid dosage form

PHARMA SCIENCE MONITOR AN INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES PHARMACOKINETIC INTERACTION OF MOXIFLOXACIN AND

Multi-residue Determination of Polar Veterinary Drugs in Livestock and Fishery Products by

DEVELOPMENT AND VALIDATION OF AMOXICILLIN AND CLAVULANATE BY USING LC-MS METHOD

Proficiency study for macrolides in porcine tissue

ABSTRACT INTRODUCTION HSIU-KUAN CHOU 1, CHIUAN-YANG LAI 1, TAY-HWA CHEN 1 AND GOW-CHIN YEN 2 *

Antibiotics Removal in Biological Sewage Treatment Plants

A validated UPLC/ESI-MS/MS bioanalytical method for the quantification of Perindopril and Amlodipine in human plasma. Kalaiyarasi.

POST SCREENING METHODS FOR THE DETECTION OF BETA-LACTAM RESIDUES IN PIGS.

HPLC method for simultaneous determination of Albendazole metabolites in plasma

Isocratic Reverse Phase High Performance Liquid Chromatographic Estimation of Ramipril and Amlodipine in Pharmaceutical Dosage Form

MULTI-CLASS PROCEDURE FOR ANALYSIS OF ANTIBACTERIAL COMPOUNDS IN EGGS BY LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY

Chemical Residue Testing and the Role of Proficiency Testing Material at the Centre for Veterinary Drug Residues

Supplementary information

Deptt of Pharma Science SGRR ITS Patel Nagar, Dehradun (UK)

Analysis of Contaminants in Food

Deborah A. Cera - Division of Compliance Center for Veterinary Medicine, FDA

Triline Pumps. Vacuum & Pressure Gas moving Engineers. Diaphragm Pumps EVM Series

LC-MS/MS Methods for the Effective Control of Veterinary Drugs in Raw Materials and Manufactured Products. A Food Industry Perspective

FOLIA VETERINARIA, 47, 3 : 2003 STANDARDS IN POULTRY MEAT AND AFTER ADMINISTRATION OF AMURIL PLV. SOL.

Accepted Manuscript. Andreia Freitas, Jorge Barbosa, Fernando Ramos. S (13) DOI: /j.idairyj Reference: INDA 3531

Introduction PAPER IN FOREFRONT. Larissa J. M. Jansen 1 & Yvette J. C. Bolck 1 & Janneau Rademaker 1 & Tina Zuidema 1 & Bjorn J. A.

Analytical Chemistry Insights 2014:9

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets

Chandra Mohan Rao Kota et al INTERNATIONAL JOURNAL OF RESEARCH AND REVIEWS IN PHARMACY AND APPLIED SCIENCES

Kamepalli Sujana et al. / Journal of Pharmacy Research 2014,8(12), Available online through

A Simple Sample Preparation with HPLC UV Method for Estimation of Amlodipine from Plasma: Application to Bioequivalence Study

Concentration of Enrofloxacin Residue from Tilapia (Oreochromis niloticus) Muscular That Infected by Aeromonas salmonicida

Premi Test. Art. No. R3900. R-Biopharm AG. Fast Determination of antibiotic residues in less than 4 hours

Transcription:

Application Note Food Testing Veterinary Drug Detection in Pork and Milk Using an Ultivo LC/TQ with a standard ESI ion source Figure 1. Agilent Ultivo LC/TQ with ESI source. Author Theresa Sosienski Agilent Technologies, Inc. Abstract This Application Note highlights a 1-minute analytical method for the precise quantification of 12 regulated veterinary drug compounds in pork and milk. The method uses an Agilent 126 Infinity II Prime LC and an Agilent Ultivo triple quadrupole LC/MS with an ESI source. The 12 veterinary drug compounds selected for evaluation in this method have maximum residue limits (MRLs) up to 1, µg/kg as defined by global regulations, and need to be analyzed at levels up to 5 the MRL. The intuitive design and easy maintenance of Ultivo make the system well suited for high-throughput detection of these veterinary drugs. Ground pork and milk were chosen to represent broad matrices with high fat and water content. This method exceeds the sensitivity requirements defined by global regulations, with high precision (RSD% <14 %) for all veterinary drug compounds included in this method.

Introduction Veterinary drugs are mainly used in livestock to prevent diseases and parasites, and promote growth. Improper use of veterinary drugs in livestock operations can result in the accumulation of these drugs in animal tissues and other animal-derived foods such as milk or eggs. Because of global concern for the presence of veterinary drugs in livestock products for human consumption, an AOAC working group recently proposed Standard Method Performance Requirements (SMPRs) for an extensive list of veterinary drug compounds. These included detection limits based on US 1, Codex 2, China 3, and Canada 4 regulations for veterinary drug residues in meat and milk. Detection limit requirements were proposed at half the MRL with the lowest MRL between the regulatory agencies always being chosen as the default. The 12 veterinary drugs included in this method represent a group of veterinary drugs that have relatively high MRLs in milk and meat. The veterinary drug compounds each have target testing levels, defined as 1/2 the MRL of the compound. The target testing levels of the 12 studied compounds range from 22.5 1 µg/kg in milk and from 5 5 µg/kg in meat (Table 1). The Ultivo triple quadrupole LC/MS with a standard ESI source can be the perfect system for such measurements. This Application Note demonstrates the precise quantification of 12 regulated veterinary drug compounds in pork and milk using a 126 Infinity II Prime LC and an Ultivo LC/TQ equipped with an ESI source. The Ultivo-ESI inherited the outstanding performance of Ultivo. Table 1. Target testing levels of the 12 veterinary drugs in milk and meat. Compound Experimental Reagents and chemicals Milk target testing level (µg/kg) 5 5 Chlortetracycline 5 5 Closantel 22.5 5 Dihydrostreptomycin 62.5 25 Diminazene 75 25 Fenbendazole 5 5 Lincomycin 75 5 Novobiocin 25 5 Oxytetracycline 5 5 1 1 Streptomycin 62.5 25 Tetracycline 5 5 All reagents used were HPLC or LC/MS grade. Acetonitrile and methanol were purchased from Honeywell (Morristown, NJ, USA), and ultrapure water was sourced from a Milli-Q Integral System with a LC-Pak Polisher and a.22-µm point-of-use membrane filter cartridge (EMD Millipore, Billerica, MA, USA). Formic acid was purchased from Fisher Scientific (Fair Lawn, NJ, USA), and ammonium fluoride (solid powder) was purchased from Aldrich (Sigma-Aldrich Corp., St. Louis, MO, USA), a 5 M stock solution was made. Veterinary drug standards were also purchased from Sigma-Aldrich. Meat target testing level (µg/kg) Sample preparation Fresh 2 % pasteurized organic milk and antibiotic-free ground pork (8 % lean, 2 % fat) were obtained from local grocery stores. Samples of 2 g of pork or milk were weighed in 5-mL polypropylene tubes, and frozen until analysis. The sample preparation procedure for pork was sourced from a method previously evaluated by Zhao; et al. 5. The method was further modified for the milk extraction, and is summarized in Figure 2. A Heidolph Hei-MIX Multi Reax system was used to vortex the samples. Agilent Captiva EMR Lipid cartridges, 6 ml, 6 mg (p/n 519-14) were used in the final cleanup of the pork extraction. Captiva EMR Lipid cartridges provide efficient and selective lipid removal with exceptional recovery of hydrophobic analytes. 2

Milk Pork Weigh 2 g of milk into a 5-mL centrifuge tube. Weigh 2 g of pork into a 5-mL centrifuge tube. Add 4 µl.5 M EDTA solution. Add 2 ml of.1 M EDTA solution and two ceramic homogenizers to the pork. Shake supernatants for 5 minutes on a vortex shaker. Shake for 5 minutes on a vortex shaker. Shake for 5 minutes on a vortex shaker. Centrifuge the supernatants at 4,5 rpm for 5 minutes. Add 7.6 ml of acetonitrile with 2 % formic acid and 2 % DMSO. Centrifuge at 4,5 rpm for 5 minutes, then transfer the supernatant. Transfer 5 ml of supernatant to a Captiva EMR Lipid cartridge, allow gravity elution, then collect the eluate. Shake for 5 minutes on a vortex shaker. Centrifuge at 4,5 rpm for 5 minutes. Add 8 ml of acetonitrile with 2 % formic acid and 2 % DMSO. Shake for 5 minutes on a vortex shaker. Combine supernatants in a 15-mL centrifuge tube. Add 5 ml of 8:2 acetonitrile/water solution, and apply gentle vacuum until no liquid remains in the cartridge. Transfer the eluate to an LC vial. Transfer the supernatant to an LC vial. Centrifuge at 4,5 rpm for 5 minutes, then transfer the supernatant. Figure 2. Sample preparation procedure for veterinary drugs in pork and milk. Instrumentation Agilent 126 Infinity II Prime LC 126 Infinity II Prime flexible pump (G714C) 126 Infinity II multisampler with cooler (G7167A) 126 Infinity II multicolumn thermostat (G7116A) Agilent Ultivo triple quadrupole LC/MS system Electrospray ionization source (G1948B) Method Table 2 summarizes the 126 Infinity II Prime LC conditions, and Table 3 summarizes the Ultivo ion source and instrument parameters. Table 4 shows the optimized MS parameters for the compounds of interest. Dynamic multiple reaction monitoring (dmrm) was used for data collection. MassHunter Quantitative Analysis software B.9 with the Quant-My-Way feature was used to accelerate and streamline the data analysis and review process. Table 2. Agilent 126 Infinity II Prime LC parameters. Column Column temperature 4 C Observed column backpressure range Injection volume 4 µl Mobile phase Flow rate Gradient Stop time Post time Table 3. Ultivo ion source and mass analyzer parameters. Gas temperature 325 C Gas flow Nebulizer pressure 8 L/min 4 psi Capillary voltage 2, V (+) Cycle time 5 ms Agilent InfinityLab Poroshell 12 EC-C8, 2.1 1 mm, 2.7 µm (p/n 695775-96) 17 37 bar A).2 % Formic acid in water B).5 mm Ammonium fluoride in methanol.35 ml/min Time (min) %B 2 1.5 2 2.5 7 5. 1 7. 1 7.1 2 9. 2 9. minutes 1. minutes 3

Experimental design Pork and milk spiked after the extraction procedure (post spiked) were used for the sensitivity, precision, and linearity studies. For recovery evaluation, pork and milk were spiked with a stock solution of veterinary drugs before extraction (prespiked), and compared to post spiked pork and milk extracts for recovery (%) calculations after analysis. Results and discussion Method sensitivity and precision All veterinary drugs could accurately be quantified at 1/2 MRL, while most could be quantified at 1/1 MRL, the lowest level tested in this study. Figure 3 shows the excellent signal response for all analytes at the target testing level in pork extract. The veterinary drugs also showed excellent precision at the lowest testing level, with RSD% below 14 % for all compounds tested, along with each compound s lowest testing level, as shown in Table 5. Accurate quantification at the lowest testing level was defined as having four out of six replicate injections with accuracy of 8 12 %, and a signal to-noise ratio (S/N) greater than 1 for both quantifiers and qualifiers. Several veterinary drug compounds had a very strong signal response at 1/1 MRL, indicating that the quantitation limit is considerably lower than 1/1 MRL (a few examples are included in Figure 4). Table 4. Optimized transitions for veterinary drug detection in dynamic MRM mode. Compound Precursor (m/z) Product (m/z) RT (min) RT Window (min) Fragmentor (V) CE (V) Polarity Dihydrostreptomycin 584.3 24.67.89 1 44 Positive Dihydrostreptomycin 584.3 2.67.89 1 32 Positive Streptomycin 599.3 582.3.67.69 16 12 Positive Streptomycin 599.3 263.67.69 16 32 Positive Diminazine 282.2 254.1 4.5.77 9 Positive Diminazine 282.2 118.9 4.5.77 9 12 Positive Lincomycin 47.2 126 4.78 1.1 15 28 Positive Lincomycin 47.2 82.2 4.78 1.1 15 8 Positive Tetracycline 445.2 427.1 4.86.81 13 4 Positive Tetracycline 445.2 41.1 4.86.81 13 8 Positive Oxytetracycline 46 443.1 4.88 1.5 13 Positive Oxytetracycline 46 426 4.88 1.5 13 12 Positive 422.2 1.9 5.93 7 2 Positive 422.2 83 5.93 7 2 Positive Chlortetracycline 479.1 444.1 5.9 1.1 14 12 Positive Chlortetracycline 479.1 26.1 5.9 1.1 14 6 Positive 524 241 5.21.97 14 8 Positive 524 124.9 5.21.97 14 68 Positive Fenbendazole 3.1 268.1 5.98 1.5 14 16 Positive Fenbendazole 3.1 159 5.98 1.5 14 36 Positive Novobiocin 613.2 133.1 6.6.85 12 68 Positive Novobiocin 613.2 132.5 6.6.85 12 72 Positive Closantel 662.9 264 7.29.8 18 28 Positive Closantel 662.9 194.1 7.29.8 18 8 Positive 4

1 4 1.3 Fenbendazole 1.1 1..9.8.7.6.5.4.3 1 1 7. 6.5 6. 5.5 5. 4.5 4. 3.5 3. 2.5 2. 1.5 1..5 Dihydrostreptomycin.5.6.7.8.9 Streptomycin Lincomycin Oxytetracycline Chlortetracycline Tetracycline Closantel.2 Diminazine.1 Novobiocin.4.6.8 1. 1.4 1.6 1.8 2. 2.2 2.4 2.6 2.8 3. 3.2 3.4 3.6 3.8 4. 4.2 4.4 4.6 4.8 5. 5.2 5.4 5.6 5.8 6. 6.2 6.4 6.6 6.8 7. 7.2 7.4 7.6 Acquisition time (min) Figure 3. Chromatogram of veterinary drug analytes spiked into pork extract at the target testing level (1/2 MRL). Table 5. Lowest testing level and precision for all veterinary drugs studied in pork and milk extract. All could accurately be quantified at or below the target testing level (1/2 MRL). Milk Pork Compound Lowest testing level (µg/kg) RSD% (n = 6) Lowest testing level (µg/kg) RSD% (n = 6) Streptomycin 1/2 MRL 62.5 13.74 1/5 MRL 1 6.92 Dihydrostreptomycin 1/2 MRL 62.5 7.76 1/5 MRL 1 6.52 Diminazine 1/1 MRL 15 5.79 1/1 MRL 5 3.74 Lincomycin 1/1 MRL 15 2.2 1/1 MRL 1.83 Tetracycline 1/1 MRL 1 3.26 1/1 MRL 1 3.48 Oxytetracycline 1/1 MRL 1 4.16 1/1 MRL 1 3.6 1/1 MRL 2 4.34 1/1 MRL 2 5.39 Chlortetracycline 1/1 MRL 1 3.38 1/1 MRL 1 3.46 1/1 MRL 1 11.56 1/1 MRL 1 2.22 Fenbendazole 1/1 MRL 1 1.1 1/1 MRL 1 6 Novobiocin 1/5 MRL 1 1.93 1/1 MRL 1 4.13 Closantel 1/1 MRL 4.5 4.75 1/1 MRL 1 3.6 5

Milk 1 2 1 + MRM (46 & 426.) 3 1 + MRM (47.2 & 126.) 3 1 + MRM (3.1 & 268.1) 3 + MRM (662.9 & 264.) 2.8 5.5 4.866 min. 1.8 4.768 min. 5.969 min. 1.7 2.6.9 7.263 min. 5. 1.6 2.4 1.5.8 4.5 1.4 2.2 1.3 2..7 4. 1.8 3.5.6 1.1 1.6 1. 3. 1.4.5.9 2.5 2. 1.5 1..5 -.5.8.7.6.5.4.3.2.1 -.1 1..8.6.4.2 -.2 4.6 4.7 4.8 4.9 5. 5.1 5.2 4.4 4.6 4.8 5. 5.2 5.7 5.8 5.9 6. 6.1 6.2 6.3 7. 7.1 7.2 7.3 7.4 7.5 7.6 Acquisition time (min) Acquisition time (min) Acquisition time (min) Acquisition time (min) Pork.4.3.2.1 Oxytetracycline in milk 1/1 MRL & 1 µg/kg Peak area: 395 S/N: 2,354 Lincomycin in milk 1/1 MRL & 15 µg/kg Peak area: 12237 S/N: 787 Fenbendazole in pork 1/1 MRL & 15 µg/kg Peak area: 1568 S/N: 114 Closantel in pork 1/1 MRL& 1 µg/kg Peak area: 492 S/N: 878 Figure 4. Select veterinary drug compounds with strong signal response at 1/1 MRL, indicating that the quantitation limit is much lower than 1/1 MRL. Method linearity All veterinary drugs showed good linearity with 1/x weighting, and all calibration curves have R 2 values greater than.98. Calibration levels ranged from 1/1 MRL to 5 MRL for all analytes. Figure 5 shows examples of some of the calibration curves. 1 4.9.8.7.6.5.4.3.2.1 1 4 7 6 5 4 3 2 1 R 2 =.998 Range: 1.6 8 µg/l 1 2 3 4 5 6 7 8 Concentration (ng/ml) R 2 =.998 Range: 16 8 µg/l 1 2 3 4 5 6 7 8 1 4 2.4 R 2 =.999 Range: 3.2 16 µg/l 2. 7 6 1.6 5 4.8 3 2.4 1 Milk Milk Milk 2 4 6 8 1 12 14 16 1 4 1 4 2. 4.5 Chlortetracycline 1.8 R 2 =.999 4. R 2 =.999 1.6 Range: 3.2 16 µg/l 3.5 Range: 1.6 8 µg/l 1.4 3. 2.5 1..8 2..6 1.5.4 1..2.5 Pork Pork Pork 2 4 6 8 1 12 14 16 1 4 Chlortetracycline R 2 =.999 Range: 1.6 8 µg/l 1 2 3 4 5 6 7 8 1 2 3 4 5 6 7 8 Figure 5. Select calibration curves of veterinary drugs spiked into pork and milk matrices at concentrations ranging from 1/1 MRL to 5 MRL. 6

Method recovery The recovery of all veterinary drugs was evaluated in both milk and pork at three levels: 1/2 MRL, MRL, and 2 MRL. Six replicates of each spiking level were evaluated in the recovery study. For 1 of the compounds, the recovery was between 6 and 12 % at all levels in both matrices (Figure 6). Dihydrostreptomycin and streptomycin had poor recovery with this extraction method, but could be detected at or below the target testing level (1/2 MRL) in post spiked matrix. For these two very hydrophilic compounds, a different extraction method may be used, but this analysis method is suitable for screening. For accurate quantitation, internal standards should be used to correct the loss of these two compounds during extraction. A Recovery (%) 15 14 13 12 11 1 9 8 7 6 5 4 3 2 1 Diminazine Lincomycin Tetracycline Oxytetracycline Chlortetracycline Fenbendazole Novobiocin Closantel 1/2 MRL MRL 2X MRL Veterinary drug compound B 13 12 11 1 9 8 7 6 5 4 3 2 1 Recovery (%) Diminazine Lincomycin Tetracycline Oxytetracycline Chlortetracycline Fenbendazole Novobiocin Closantel 1/2 MRL MRL 2X MRL Veterinary drug compound Figure 6. Recovery of veterinary drugs in milk (A) and pork (B) at 1/2 MRL, MRL, and 2 MRL spiking levels. Error bars denote the standard deviation of six replicates. Dihydrostreptomycin and streptomycin are not included. 7

Conclusions The use of an Ultivo triple quadrupole LC/MS equipped with an ESI ion source exceeded the MRL requirements set by global regulatory agencies for veterinary drugs in meat and milk, with excellent precision. Captiva EMR Lipid cartridges provided adequate extra cleanup of the fat-laden pork matrix, assisting the method sensitivity. The 126 Infinity II Prime LC was a perfect separation tool for the low backpressure observed with this method. In applications where the sensitivity requirements can be relaxed, this configuration of Ultivo with an ESI source is an excellent fit-for-purpose choice. References 1. Department of Health and Human Services, Food and Drug Administration, 21 CFR Parts 514 and 558, FDA-21-N-155. 2. Proposal for a regulation of the European Parliament and of the council on veterinary medicinal products, European Commission, 214/257 (COD). 3. Maximum Residue Limits in animal derived foods, Announcement No. 235, Ministry of Agriculture, China, 22. 4. List of Maximum Residue Limits (MRLs) for Veterinary Drugs in Foods, Health Canada, Government of Canada. August 2, 217. https:// www.canada.ca/content/dam/ hc-sc/migration/hc-sc/dhp-mps/ alt_formats/pdf/vet/mrl-lmr/mrl- lmr_versus_new-nouveau-21782- eng.pdf 5. Zhao, L.; Lucas, D. Multiclass Multiresidue Veterinary Drug Analysis in Beef Using Agilent Captiva EMR Lipid Cartridge Cleanup and LC/MS/MS. Agilent Technologies Application Note, publication number 5991 8598EN, 217. www.agilent.com/chem This information is subject to change without notice. Agilent Technologies, Inc. 218 Printed in the USA, December 13, 218 5994-48EN