Benzo[a]pyrene Method Development

Similar documents
How To Develop A Recipe Card

Step-by-Step Analytical Methods Validation and Protocol in the Quality System Compliance Industry

Cigarette Variability Task Force: CVAR

Chemistry 321, Experiment 8: Quantitation of caffeine from a beverage using gas chromatography

Chemical analysis service, Turner s Green Technology Group

How To Test For Contamination In Large Volume Water

CORESTA RECOMMENDED METHOD Nº 80

CORESTA RECOMMENDED METHOD N 72

Analysis of Polyphenols in Fruit Juices Using ACQUITY UPLC H-Class with UV and MS Detection

Fast, Reproducible LC-MS/MS Analysis of Dextromethorphan and Dextrorphan

MEPS - Micro Extraction by Packed Sorbent Online SPE for GC and LC sample preparation - Extraction to injection in a single process

Thermo Scientific SOLAµ SPE Plates Technical Guide. Consistent excellence. for bioanalysis

Determination of Polycyclic Aromatic Hydrocarbons (PAH) in Food with GC-MS/MS

Vitamin C quantification using reversed-phase ion-pairing HPLC

Extraction of Epinephrine, Norepinephrine and Dopamine from Human Plasma Using EVOLUTE EXPRESS WCX Prior to LC-MS/MS Analysis

Overview. Triple quadrupole (MS/MS) systems provide in comparison to single quadrupole (MS) systems: Introduction

Analysis of Free Bromate Ions in Tap Water using an ACQUITY UPLC BEH Amide Column

LC-MS/MS Method for the Determination of Docetaxel in Human Serum for Clinical Research

CONFIRMATION OF ZOLPIDEM BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY

Analysis of the Vitamin B Complex in Infant Formula Samples by LC-MS/MS

ANALYTICAL METHODS INTERNATIONAL QUALITY SYSTEMS

LC-MS/MS, the new reference method for mycotoxin analysis

Analysis of Phthalate Esters in Children's Toys Using GC-MS

Expectations for GC-MS Lab

Technical Report. Automatic Identification and Semi-quantitative Analysis of Psychotropic Drugs in Serum Using GC/MS Forensic Toxicological Database

Alignment and Preprocessing for Data Analysis

Simultaneous determination of L-ascorbic acid and D-iso-ascorbic acid (erythorbic acid) in wine by HPLC and UV-detection (Resolution Oeno 11/2008)

UHPLC/MS: An Efficient Tool for Determination of Illicit Drugs

Indoor Air Comfort Test Report

Determination of Anabolic Steroids in Horse Urine by SPE and LC-MS/MS

Extraction of Cannabinoids in Marijuana and Edibles by QuEChERS

The First Quantitative Analysis of Alkylated PAH and PASH by GCxGC/MS and its Implications on Weathering Studies

Setting up a Quantitative Analysis MS ChemStation

High sensitivity assays using online SPE-LC-MS/MS -How low can you go? Mohammed Abrar Unilabs York Bioanalytical solutions, York, UK

Shimadzu Simulated Distillation Gas Chromatograph System C184-E030

Thermo Scientific HyperSep Solid Phase Extraction Method Development Guide

Guide to Reverse Phase SpinColumns Chromatography for Sample Prep

Method development for analysis of formaldehyde in foodsimulant. melamine-ware by GC-MS and LC-MS/MS. Internal Technical Report

LC-MS/MS for Chromatographers

GENERAL UNKNOWN SCREENING FOR DRUGS IN BIOLOGICAL SAMPLES BY LC/MS Luc Humbert1, Michel Lhermitte 1, Frederic Grisel 2 1

Application Note. Determination of Nitrite and Nitrate in Fruit Juices by UV Detection. Summary. Introduction. Experimental Sample Preparation

Standard Analytical Methods of Bioactive Metabolitesfrom Lonicera japonica Flower Buds by HPLC-DAD and HPLC-MS/MS

Paper Chromatography: Separation and Identification of Five Metal Cations

Determination of Pesticide Residues in Drinking Water Using Automated Solid-Phase Extraction and Gas Chromatography with Nitrogen Phosphorus Detection

Quantitative analysis of anabolic steroids in control samples from food-producing animals using a column-switching LC-HESI-MS/MS assay

Amino Acid Analyzer L-8900

Daniel M. Mueller, Katharina M. Rentsch Institut für Klinische Chemie, Universitätsspital Zürich, CH-8091 Zürich, Schweiz

# LCMS-35 esquire series. Application of LC/APCI Ion Trap Tandem Mass Spectrometry for the Multiresidue Analysis of Pesticides in Water

Purification of reaction mixtures using flash chromatography.

A VISION to On-Line SPE PTV GC MS Determination of Organic Micro Pollutants in Surface Water

Online SPE-LC-APCI-MS/MS for the Determination of Steroidal Hormones in Drinking Water

AppsLab Library. A new online platform for Thermo Fisher Scientific applications and methods. Susanne Kramer, Ph.D. Product Manager AppsLab Library

SPE, LC-MS/MS Method for the Determination of Ethinyl Estradiol from Human Plasma

Develop a Quantitative Analytical Method for low (» 1 ppm) levels of Sulfate

Reference Materials for Environmental Performance Testing Dr Steve Wood Head of Regulatory and Legislative Services. ISPRA 25 June 2009

A commitment to quality and continuous improvement

Application Note # MS-14 Fast On-site Identification of Drugs with the mobile GC/MS system E²M

Gas Chromatography Liner Selection Guide

Using Natural Products Application Solution with UNIFI for the Identification of Chemical Ingredients of Green Tea Extract

STANDARD OPERATING PROCEDURES

Advantages of Polar, Reversed- Phase HPLC Columns for the Analysis of Drug Metabolites

Increasing the Multiplexing of High Resolution Targeted Peptide Quantification Assays

Automation of Solid Phase Extraction and Column Chromatographic Cleanup

Training Courses 2014 HPLC GC SPE

Selective Testosterone Analysis in Human Serum by LC-FAIMS-MS/MS

Determination of Caffeine in Beverages HPLC-1

The Automated SPE Assay of Fipronil and Its Metabolites from Bee Pollen.

The Theory of HPLC. Gradient HPLC

Application of TargetView software within the food industry - the identi cation of pyrazine compounds in potato crisps

Pesticide Analysis by Mass Spectrometry

Sensitive and Rapid Determination of Polycyclic Aromatic Hydrocarbons in Tap Water

ANALYSIS OF FOOD AND NATURAL PRODUCTS LABORATORY EXERCISE

TargetQuan 3 Software. Leading the way in regulatory. POPs quantification. Bullet Bullet Bullet

Enhancing GCMS analysis of trace compounds using a new dynamic baseline compensation algorithm to reduce background interference

Strategies for Developing Optimal Synchronous SIM-Scan Acquisition Methods AutoSIM/Scan Setup and Rapid SIM. Technical Overview.

Thermo Scientific SOLA SPE cartridges and plates Technical Guide. Join the revolution. unparalleled performance

Proficiency Testing In A Global Analytical Environment Benefits & Challenges. AOAC September 2007

Application of Structure-Based LC/MS Database Management for Forensic Analysis

EFFECT OF CERTAIN LIQUID FILTER ADDITIVES ON MENTHOL DELIVERY

APPENDIX C. DATA VALIDATION REPORT

LIQUID CHROMATOGRAPHY HOW MUCH ASPIRIN, ACETAMINOPHEN, AND CAFFEINE ARE IN YOUR PAIN RELIEVER? USING HPLC TO QUANTITATE SUBSTANCES (Revised: )

Fipronil Analysis By GC/XSD following Post-Extraction Gel Permeation Chromatography Cleanup

Simultaneous Qualitative and Quantitative Data Acquisition for Research of Diabetes Drugs

The Essential CHROMacademy Guide. Mobile Phase Optimization Strategies for Reversed Phase HPLC

1.1 This test method covers the qualitative and quantitative determination of the content of benzene and toluene in hydrocarbon wax.

Thermo Scientific Dionex Chromeleon 7 Chromatography Data System Software

AppNote 6/2003. Analysis of Flavors using a Mass Spectral Based Chemical Sensor KEYWORDS ABSTRACT

Intelligent use of Relative Response Factors in Gas Chromatography-Flame Ionisation Detection

Therapeutic Drug Monitoring of Antiretroviral Drugs with HPLC-MS

Conversion of a USP Gas Chromatography Method to Convergence Chromatography: Analysis of Atropa Belladonna

Simultaneous Metabolite Identification and Quantitation with UV Data Integration Using LightSight Software Version 2.2

An Advanced Base Deactivated Capillary Column for analysis of Volatile amines Ammonia and Alcohols.

Implementing New USP Chapters for Analytical Method Validation

Introduction. The following definitions may help you better understand the components of the data report.

Analysis of Drugs by using the Ultra Inert Inlet Liners with Wool

Transcription:

Benzo[a]pyrene Method Development Dr Michael Intorp CORESTA Cooperation Center for Scientific Research Relative to Tobacco FDA Center for Tobacco Products Scientific Workshop Tobacco Product Analysis 30 31 July 2013

Creation Set up in 1999 initially as a Task Force Background Growing regulatory interest Lack of standardised methods Measurement reproducibility not established Objective CORESTA Special Analytes Sub-Group Propose practical and robust recommended methods for compounds in cigarette mainstream smoke (CORESTA Recommended Methods, CRMs) Work Program One of the priority compounds was identified as benzo[a]pyrene 2

CORESTA Special Analytes Sub-Group Development of Recommended Methods Approach used for the development of robust methods Should involve a relatively large number of laboratories CORESTA well represents global expertise in this type of measurement. There are more than 20 active laboratories from 12 countries Should involve a wide range of product and design styles Range of blend styles Range of tar yields Manufactured in various global regions Consensual and unanimous decisions on standardisation 3

B[a]P method development between 1999 and 2003 Review of existing methods for cigarette smoke Two types of methods were identified (HPLC-FLD and GC-MS) Both types required matrix reduction (clean up) Joint experiments using HPLC-FLD methods Decision was based on most widely used method (HPLC-FLD) However, reduction of initially observed variability appeared technically difficult (poor separation from other components) Investigation of GC-MS methods as alternative Collaborative study results demonstrated lower between laboratory variability compared to HPLC-FLD 4

Laboratory B[a]P method comparison: HPLC-FLD versus GC-MS Data from 12 laboratories on the 2R4F reference cigarette Benzo[a]pyrene (ng/cig) under ISO smoking regime HPLC GC-MS Mean SD RSD (%) Mean SD RSD (%) Statistical Difference (ISO 5725-2) HPLC v GS-MS 1 5.10 0.60 11.6 7.50 0.50 6.2 yes 2 4.98 0.74 14.9 6.80 0.44 6.5 yes 3 3.20 0.72 27.4 5.60 0.33 5.8 yes 4 2.69 0.53 19.8 5.25 0.20 3.9 yes 5 5.12 0.54 10.5 5.72 0.10 1.7 no 6 2.36 0.50 21.2 5.49 0.80 14.6 n/a 7 4.92 0.60 12.2 - - - - 8 5.87 0.20 3.3 4.60 0.18 3.8 yes 9 6.08 0.91 14.9 7.28 1.15 15.7 no 10 4.95 0.35 7.1 4.97 0.16 3.3 no 11 5.28 0.46 8.7 5.54 0.39 7.0 no 12 4.07 0.27 6.7 4.71 0.30 6.5 yes Mean across all data 4.55 1.21 26.5 5.77 0.99 17.3 5

Benzo[a]pyrene GC-MS method Analytical details Conditioning and machine smoking according to ISO 3402 and ISO 3308. Methanol extraction of the total particulate matter collected on the glass-fibre filter pad and dilution with water. Clean up through solid phase extraction (CH), followed by the elution of B[a]P with cyclohexane. Analytical determination using single ion monitoring (SIM) detection mode. Ion traces for quantification and confirmation: B[a]P: m/z 252 (quantification) and 250 (confirmation) B[a]P-d12: m/z 264 (quantification) and 260 (confirmation) 6

Benzo[a]pyrene GC-MS method Analytical details 30 m capillary column with a methylphenyl (5 %) polysiloxane stationary phase, 0.25 mm id and 0.25 µm film. Retention times of the B[a]P and B[a]P-d12 peaks are between 40 and 45 minutes. B[a]P d12 B[a]P The upper chromatogram shows the portion of chromatogram located between 40 and 65 min and the lower one is a zoom around the B[a]P and B[a]Pd12 peaks 7

Benzo[a]pyrene GC-MS method Collaborative Study 2003 13 laboratories (8 countries) 7 test cigarettes ISO 3308 smoking Repeatability (r) and Reproducibility (R) estimates by ISO 5725-2 Cigarette Mean (ng/cig) r (ng/cig) R (ng/cig) R% 2R4F 7.3 1.3 2.5 35 A 1.8 0.5 1.0 56 B 5.3 1.1 2.5 48 C 6.5 1.1 2.2 34 D 7.8 1.5 2.9 37 E 8.7 1.4 2.7 31 F 14.1 2.3 5.9 42 8

Benzo[a]pyrene GC-MS method Collaborative Study 2011 Statistical Data obtained from Collaborative Study 2011 outliers removed 12 laboratories (maximum) / 10 test cigarettes Cigarette Sample ISO 3308 regime Benzo[a]pyrene (ng/cig) Health Canada T-115 regime N Mean r R R% N Mean r R R% CM6 10 15.48 2.48 5.19 33.5 11 27.86 4.65 8.45 30.3 1R5F 10 1.64 0.41 0.80 48.8 12 7.13 1.25 2.28 32.0 3R4F 11 6.66 0.85 2.00 30.0 12 15.51 1.68 4.93 31.8 1 10 8.49 2.00 3.11 36.6 9 17.81 3.06 6.79 38.1 2 10 8.00 1.26 2.15 26.9 9 18.37 1.88 4.85 26.4 3 9 8.22 1.24 2.57 31.3 10 20.69 4.88 7.85 37.9 4 8 3.84 0.69 1.74 45.3 9 10.63 1.97 3.67 34.5 5 8 2.14 0.55 1.32 61.7 10 7.52 1.67 2.93 39.0 6 9 7.66 0.99 2.69 35.1 9 14.24 2.28 4.85 34.1 7 8 1.85 0.58 1.14 61.6 10 9.12 1.83 3.98 43.6 General increase in R and decrease in R% with increasing BaP yields for both regimes 9

Benzo[a]pyrene - R (ng/cig) 9 8 7 CRM 58 BaP 2003 - ISO CRM 58 BaP 2012 - ISO CRM 58 BaP 2012 - HCI Benzo[a]pyrene R versus Mean yield from CRM 58 6 5 4 3 2 1 0 0 5 10 15 20 25 30 Benzo[a]pyrene - Mean (ng/cig) 10

Conclusions & Achievements CRM 58 was developed for BaP in cigarette mainstream smoke and is on the CORESTA website. Some observations on data variability is being made publicly available in a Beiträge publication. Round-table discussions during development provide valuable insight into causes and ways to reduce inter-laboratory data variability Inter-laboratory variability from collaborative studies is still higher compared to TNCO even when working to a CRM. 11

Benzo[a]pyrene Method Development Summary 2003 Collaborative Study - GC-MS method - 13 labs ISO 3308 2004 Optimised method published as CRM 58 2008 Published as international standard (ISO 22634) 2011 Collaborative study (11 labs) using ISO 3308 and HC T-115 2013 Revision of CRM 58 including HCI data on CORESTA website 2013 Publication submitted to Beiträge 12

Outlook CORESTA Special Analytes Sub-Group provides a valuable forum for method development, in this example for BaP in cigarette mainstream smoke. Bringing together the wide ranging global expertise represented by the tobacco manufacturers, contract laboratories, governmental and other laboratories has led to: Open discussions and the readiness of members to modify their internal methodologies Advantages for participating laboratories to make use of shared knowledge Significant optimisation of many aspects of the methodology Participation in collaborative studies has helped with aspects of laboratory accreditation under ISO 17025 or equivalent. Learnings are incorporated in the final Recommended Methods and are also recorded via papers published by the Sub-Group 13

Appendix - Publications Purkis, S., Intorp, M., Hauleithner, A., Updates of CORESTA Recommended Methods after further collaborative studies carried out under both ISO and Health Canada Intense smoking regimes; Beitr. TabakForsch. Int. 2013 submitted to Journal. 14

Questions? 15