EURL-SRM - Analytical Observations Report

Similar documents
Analysis of Pyridate and its metabolite Pyridafol by QuEChERS and LC-MS/MS

Matrix-induced Signal Enhancement of Propamocarb in LC-MS/MS

EURL-SRM - Analytical Observations Report

EURL-SRM - Analytical Method Report. Analysis of Residues of Carbofuran (sum) Using QuEChERS Method

EURL-SRM - Analytical Observations Report

Analysis of Organotin-Pesticides by the QuEChERS Method - Impact of acidifying on the recoveries

Determination of Prochloraz (sum) via its Metabolites

Improvement of Ethoxyquin Recoveries by QuEChERS Through the Addition of Ascorbic Acid Initiator/Institution: EURL-SRM

Determination of Prochloraz (sum) via its Metabolites

Extraction of Multiple Mycotoxins From Grain Using ISOLUTE Myco prior to LC-MS/MS Analysis

Extraction of Multiple Mycotoxins From Nuts Using ISOLUTE Myco prior to LC-MS/MS Analysis

Analysis of Limonin in Citrus Juice Using QuEChERS and LC-MS/MS

Meeting Challenging Requirements for the Quantitation of Regulated Growth Promoters Dexamethasone and Betamethasone in Liver and Milk

Fast, Robust and Reliable Method for the Identification and Quantitation of Sildenafil Residue in Honey using LC-MS/MS

Validation Report 23 B

Rapid, Simple Impurity Characterization with the Xevo TQ Mass Spectrometer

Determination of Pharmaceutical Residues in Bovine Milk via LC MS/MS Following Solid Phase Extraction

Rapid Analysis of Bisphenols A, B, and E in Baby Food and Infant Formula Using ACQUITY UPLC with the Xevo TQD

Implementation Report on the patient safety Recommendation 2009/C 151/01. Healthcare Systems Unit DG SANCO

Fast and simultaneous analysis of ethanol metabolites and barbiturates using the QTRAP 4500 LC-MS/MS system

Validation Report 20

SUPPORTING INFORMATION FOR: CONCENTRATIONS OF POLYBROMINATED DIPHENYL ETHERS, HEXABROMOCYCLODODECANES AND TETRABROMOBISPHENOL-A IN BREAST MILK FROM

Supplementary Information. Effects of Perfluorooctanoic Acid on Metabolic Profiles in Brain and Liver of Mouse by a

Validation Report 8. EURL for Cereals and Feeding stuff National Food Institute Technical University of Denmark

Extraction of Aflatoxin M1 From Infant Formula Using ISOLUTE Myco SPE Columns prior to LC-MS/MS Analysis

UPLC/MS Monitoring of Water-Soluble Vitamin Bs in Cell Culture Media in Minutes

Dr. Erin E. Chambers Waters Corporation. Presented by Dr. Diego Rodriguez Cabaleiro Waters Europe Waters Corporation 1

FOOD IRRADIATION within the EU

Rapid Analysis of Water-Soluble Vitamins in Infant Formula by Standard-Addition

5.24 METHOXYFENOZIDE (209)

EURL-SRM - Analytical Observations Report

Determination of Patulin in Apple Juice Using SPE and UHPLC-MS/MS Analysis

Noora Perkola Finnish Environment Institute. Nordic MS Symposium November 9, 2011, Båstad, Sweden

Development and Validation of an UPLC-MS/MS Method for Quantification of Mycotoxins in Tobacco and Smokeless Tobacco Products

Direct Analysis of Folic Acid in Digestive Juices by LC/TOF-MS Application

Development of a Bioanalytical Method for Quantification of Amyloid Beta Peptides in Cerebrospinal Fluid

A NOVEL METHOD OF M/Z DRIFT CORRECTION FOR OA-TOF MASS SPECTROMETERS BASED ON CONSTRUCTION OF LIBRARIES OF MATRIX COMPONENTS.

Polar Pesticides Method Update

UPLC-MS/MS Analysis of Azole Antifungals in Serum for Clinical Research

EU School Fruit, Vegetables & Milk Scheme 2017/2023

Application Note. Author. Abstract. Introduction. Food Safety

Reduced Ion Suppression and Improved LC/MS Sensitivity with Agilent Bond Elut Plexa

REASONED OPINION. European Food Safety Authority 2, 3. European Food Safety Authority (EFSA), Parma, Italy

Determination of β2-agonists in Pork Using Agilent SampliQ SCX Solid-Phase Extraction Cartridges and Liquid Chromatography-Tandem Mass Spectrometry

Evaluation of active substances in plant protection products Residues Anja Friel European Food Safetey Authority, Parma/ Italy

MALAYSIAN MALAYSIAN COCOA WORKSHOP ON THE SAFE USE OF PESTICIDES IN COCOA AND HARMONIZED

Application Note No. 119/2013 Determination of bisphenol A in preserved food SpeedExtractor E-916: Determination of bisphenol A in preserved food

Fully Automated Online Sample Preparation AND Quantification of Amiodarone from Whole Blood using CLAM-LC-MS/MS

Analysis of Food Sugars in Various Matrices Using UPLC with Refractive Index (RI) Detection

Public administration reforms and public sector performance in Central and Eastern Europe EU member states: in EU perspective

A Robustness Study for the Agilent 6470 LC-MS/MS Mass Spectrometer

Development of a High Sensitivity SPE-LC-MS/MS Assay for the Quantification of Glucagon in Human Plasma Using the ionkey/ms System

ApplicationNOTE A MULTI-RESIDUE LC/MS/MS METHOD FOR THE DETERMINATION OF 81 PESTICIDE RESIDUES IN FRUIT AND VEGETABLES: PART 1, METHOD OVERVIEW

August Determination of Pindone in Agricultural Products by LC-MS/MS

ACQUITY UPLC WITH PDA DETECTION: DETERMINING THE SENSITIVITY LIMITS OF OXYBUTYNIN AND RELATED COMPOUNDS

Determination of 6-Chloropicolinic Acid (6-CPA) in Crops by Liquid Chromatography with Tandem Mass Spectrometry Detection. EPL-BAS Method No.

Matrix Factor Determination with the Waters Regulated Bioanalysis System Solution

REPORT FROM THE COMMISSION TO THE EUROPEAN PARLIAMENT AND THE COUNCIL ON FOOD INGREDIENTS TREATED WITH IONISING RADIATION FOR THE YEAR 2012

Development and Validation of Multiresidue Pesticide Methods at FDA/CFSAN

Setting of new MRLs for fluxapyroxad (BAS 700 F) in various commodities of plant and animal origin 1

2008 Annual Report on Pesticide Residues. according to Article 32 of Regulation (EC) No 396/2005 1

Pesticide Residue Analysis in Whole Milk by QuEChERS and LC-MS/MS

Results of the Survey addressed to the EU Member States about quantification of food waste and preventing Food waste Brussels,

Reasoned opinion on the review of the existing maximum residue levels (MRLs) for benalaxyl according to Article 12 of Regulation (EC) No 396/2005 1

REASONED OPINION. European Food Safety Authority 2. European Food Safety Authority (EFSA), Parma, Italy

REASONED OPINION. European Food Safety Authority 2, 3. European Food Safety Authority (EFSA), Parma, Italy

LIMITE EN COUNCIL OF THE EUROPEAN UNION. Brussels, 7 July /11 LIMITE ENFOPOL 228 DAPIX 81

Amadeo R. Fernández-Alba

High-Throughput, Cost-Efficient LC-MS/MS Forensic Method for Measuring Buprenorphine and Norbuprenorphine in Urine

Reasoned opinion on the modification of the existing MRLs for mepiquat in oats, wheat and food commodities of animal origin 1

Dienes Derivatization MaxSpec Kit

Quantitation of Protein Phosphorylation Using Multiple Reaction Monitoring

IMAZAPYR (267) First draft prepared by Mr M Irie, Ministry of Agriculture, Forestry and Fisheries, Tokyo, Japan

A RAPID AND SENSITIVE ANALYSIS METHOD OF SUDAN RED I, II, III & IV IN TOMATO SAUCE USING ULTRA PERFORMANCE LC MS/MS

Overview. Introduction. Experimental. Cliquid Software for Routine LC/MS/MS Analysis

Key Advantages of Comprehensive Cannabis Analysis

Amphetamines, Phentermine, and Designer Stimulant Quantitation Using an Agilent 6430 LC/MS/MS

Application Note: 425. Introduction. Goal. Experimental Conditions

Quantitative Analysis of Vit D Metabolites in Human Plasma using Exactive System

Probing for Packaging Migrants in a Pharmaceutical Impurities Assay Using UHPLC with UV and Mass Detection INTRODUCTION

Comprehensive Forensic Toxicology Screening in Serum using On-Line SPE LC-MS/MS

The use of mobile-device data to better estimate dynamic population size for wastewater-based epidemiology

[ APPLICATION NOTE ] Oasis PRiME HLB Cartridge for Cleanup of Infant Formula Extracts Prior to UPLC-MS/MS Multiresidue Veterinary Drugs Analysis

Non-reproductive tissues and cells

Uptake and Metabolism of Phthalate Esters by Edible Plants

5.8 DIMETHOMORPH (225)

5.23 PROPAMOCARB (148)

Modification of the existing MRLs for chlorothalonil in barley and several food commodities of animal origin 1

A High Sensitivity UPLC/MS/MS Method for the Analysis of Clopidogrel and Clopidogrel Carboxylic Acid Metabolite in Human K 2 EDTA Plasma

Determination of Chlorophenoxyacetic Acid and Other Acidic Herbicides Using a QuEChERS Sample Preparation Approach and LC-MS/MS Analysis

MS/MS as an LC Detector for the Screening of Drugs and Their Metabolites in Race Horse Urine

Boscalid BOSCALID (221)

Abstract. Introduction

A FORENSIC TOXICOLOGY METHOD FOR THE DETERMINATION OF DESOMORPHINE, HEROIN, METHADONE, BUPRENORPHINE AND METABOLITES IN URINE USING LC/MS QQQ

Modernizing the Forensic Lab with LC-MS/MS Technology

Quantitative Analysis of THC and Main Metabolites in Whole Blood Using Tandem Mass Spectrometry and Automated Online Sample Preparation

Improved Isolation and Analysis of Mycotoxins from Cereals, Beer and Wine

Sunil Kulkarni Product Specialist Agilent Technologies

Review of the existing maximum residue levels (MRLs) for oxamyl according to Article 12 of Regulation (EC) No 396/2005 1

DEXAMETHASONE. First draft prepared by Bruno LE BIZEC, Nantes, France

Transcription:

concerning the following EURL-SRM - Analytical Observations Report o Compound(s): AMTT (metabolite of tritosulfuron) o Commodities: Fruit and vegetables, cereals o Extraction Method(s): o Instrumental analysis: LC-MS/MS Analysis of the Tritosulfuron Metabolite AMTT by Method using LC-MS/MS Version 1 (last update: 30.03.2017) Background information / Initial Observations: AMTT results from the use of tritosulfuron. It is both a metabolite of tritosulfuron as well as an impurity in formulations (specification max. 0.2 g/kg) 1. Tritosulfuron is intended to be used in cereals (autumn and spring sown) and in maize. It is a post-emergence herbicide with systemic action. Due to the high toxicity of AMTT, EFSA in its reasoned opinion on Tritosulfuron in 2015 2, proposed to distinctly regulate AMTT proposing very low MRLs at 0.001 mg/kg for cereals and various products of animal origin. Based on the metabolism study it was concluded that the residues in milk were expected to be so low, that no exceedances of the toxicological thresholds are expected. The development of a method for milk that is validated at 0.0005 mg/kg was advised. With regulation 2016/2016/EC, applicable from 14 January 2017 onwards, the maximum residue level of AMTT for milk and cereals was set at 0.001 mg/kg and for all other products at 0.01 mg/kg. In the preamble of this regulation it is indicated that Analytical methods to achieve the lowest possible LOD need to be developed for AMTT. Once those methods are available, the levels set by this Regulation may be reviewed at any stage. Initial tests have shown that using unmodified and routine instrument settings of an older generation LC-MS/MS instrument (ABI-Sciex 4000), LOQs below 0.01 mg/kg are difficult to achieve, especially for dry commodities, where the sample weight is reduced to 5 g. 1 http://www.bvl.bund.de/shareddocs/downloads/04_pflanzenschutzmittel/02_eu_berichte/tritosulfuron-dar.pdf? blob=publicationfile 2 Reasoned opinion on the review of the existing maximum residue levels (MRLs) for tritosulfuron according to Article 12 of Regulation (EC) No 396/2005 EFSA Journal 2015;13(1):3964 Page 1

Compound details AMTT (CAS: 5311-05-7 ), IUPAC: 4-Methoxy-6-(trifluoromethyl)-1,3,5-triazin-2-amine 2-amino-4-methoxy-6-(trifluormethyl)-1,3,5-triazine Parameter Value Molecular Mass Exact mass 194.117 g/mol 194.04154 Da Pka not ionized when ph < 13 (Chemicalize.org) 3 LogD Residue definition EU Tritosulfuron is approved in ADI / ARfD 1.65 (calculated by Chemicalize.org) 0.62 (20 C/pH7) according to BASF-report 4 2-amino-4-methoxy-6-(trifluormethyl)-1,3,5-triazine (AMTT), resulting from the use of tritosulfuron AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SI, SK 0.0001 mg/kg bw per day / 0.0001 mg/kg bw (EC2008) Materials 5 : Substance Purity CAS Source Tritosulfuron 98.5% 142469-14-5 LGC (Dr. Ehrenstorfer) AMTT 99.9% 5311-05-7 BASF (friendly donation) Chlorpyrifos D10 97.0% 285138-81-0 LGC (Dr. Ehrenstorfer) All other materials and chemicals used as listed in EN 15662 Measurement conditions Measurement was conducted by LC-MS/MS instrument (ESI-positive mode). Details are given in Table 2 and Table 3 Table 2: Instrumentation details LC WATERS Acquity UPLC MS/MS SCIEX API 5500 Q-Trap, run in ESI positive mode Column Acquity BEH C18, 2.1x100 mm, 1.7 µm Pre-column Acquity BEH C18, 2.1x5 mm, 1.7 µm Mobile Phase A: 5 mmol NH 4 formate in purified water + 5% methanol B: 5 mmol NH 4 formate in methanol Gradient Time (min) Mobile Phase A (%) Mobile Phase B (%) 0 60 40 10 10 90 13 10 90 13.1 60 40 19 60 40 Flow 0.4 ml min -1 Injection volume 2 µl, partial loop with needle overfill Column temperature 40 C 3 Chemicalize.org 4 https://www.agrar.basf.de/agroportal/de/media/migrated/de/productfiles/sdb/sdb-arrat.pdf 5 Disclaimer: Names of companies are given for the convenience of the reader and do not indicate any preference by the EURL-SRM towards these companies and their products Page 2

Table 3: MRM details for AMTT (ESI-pos. mode using Sciex API 4000 QTrap): Compound Intensity ranking Q 1 Q 3 DP CE CXP AMTT 3 195 57 66 37 4 2 195 69 66 69 2 4 195 110 66 35 6 1 195 175 66 23 10 5 195 138 66 27 8 Chlorpyrifos D10-360 199 66 23 12 Note: If you measure on an API 5500 instrument you may also use the settings above. DP values could be increased by 20. Experiments conducted and observations: The validation experiments were based on common procedure (EN-15662 6 ). The main focus of validation experiments was on cereals. Various cleanup approaches tested (PSA, C18 or freeze out) had no negative effect on recovery. A summary of the validation experiments is given in Table 4. The results were evaluated with Chlorpyriphos-D10 as internal standard. For mean recovery and RSD only the target MRM of m/z 195/175 was used. All samples, except the 0.02 ppm level of flour, were measured with the more sensitive API5500 instrument. The 0.02 ppm validation level of flour was run on an API 4000. Comparison of API4000 and the more sensitive API5500 is shown in Figure 1. Some exemplary chromatograms showing the various MRM transition when analyzing by API5500 are shown in Figure 2. Table 4: Recovery data for AMTT from various commodities: Matrix Type Matrix Sample Weight + water addition High water Cucumber 10 g High water + low ph Dry Orange Juice Flour 10 g 5 g + 10 ml water Animal Milk 5 g *measured Origin with API4000 + 5 ml water ** matrix interference in qualifier Spiking Level n w/o cleanup Rec.% RSD % 0.001 5 98 3.4 0.01 5 100 1.6 0.001** 5 108 7.0 0.01 5 96 1.6 0.001 5 113 7.6 n with PSA/C18 Rec.% RSD % n 0.002 5 94 6.1 0.005 5 94 3.8 0.01 5 105 3.5 0.02* 5 109 7.8 5 102 11.9 with freeze out Rec.% RSD % 0.001 5 109 19.0 6 Detailed instructions on the method are given in the CEN method EN 15662 (citrate buffered), see also brief description under www.quechers.de. Page 3

Figure 1: Comparison of sensitivity between API 4000 and API 5500 instrument, exemplary with a recovery sample of 0.02 ppm AMTT on flour Instrument m/z 195/175 (target) m/z 195/69 m/z 195/57 m/z 195/110 API4000 API5500 Figure 2: Exemplary chromatograms of 0.001ppm in different matrices measured with API 5500 Matrix m/z 195/175 (target) m/z 195/69 m/z 195/57 m/z 195/110 Cucumber Orange juice (matrix interference on qualifier!) Flour Milk Page 4

Discussion and conclusions: It was shown that AMTT gives good recoveries using the citrate buffered method and that the very low MRLs in cereals and milk (at 0.001 mg/kg) can be routinely enforced but only if high end instrumentation is used. Cleanup with various approaches (PSA, C18 or freeze out) had no negative effect on recovery. Tritosulfuron (parent) is also amenable and may be measured via LC-MS/MS in ESI neg. or ESI pos. mode, but sensitivity in negative mode is much higher (f=40). History Action When Document Version Initial Experiments Oct - Dec 2015 Further Experiments Jan August 2016 Observation document placed on-line March 2017 V1 Page 5