Quantitation of Ethyl Glucuronide and Ethyl Sulfate in Urine using LC-MS/MS

Similar documents
Benzodiazepines and Barbiturates

Definitive EtG/EtS LC-MS/MS Analysis:

High-sensitivity, high-throughput quantitation of catecholamine metabolites in urine by LC/MS/MS for clinical research

Simultaneous analysis for forensic drugs in human blood and urine using ultra-high speed LC-MS/MS

Development of high speed CYP cocktail inhibition assay using UHPLC-MS/MS

Quantitative Analysis of EtG and EtS in Urine Using FASt ETG and LC-MS/MS

Analysis of Opioids Using Isotope Dilution with GCMS-TQ8030 GC/MS/MS. No. GCMS No. SSI-GCMS-1401

Quantitative Analysis of Opioids Using a Triple-Quadrupole GC/MS/MS

Highly sensitive quantitative estimation of genotoxic impurities from API and drug formulation using LC/MS/MS

Quantitative Analysis of EtG and EtS in Urine Using FASt ETG and LC-MS/MS

Multi-residue analysis of pesticides in crude food extracts using a simple extraction technique and LC/MS/MS

Analytical determination of testosterone in human serum using an Agilent Ultivo Triple Quadrupole LC/MS

Analysis of Residual Solvents in Pharmaceuticals (USP<467>) with Shimadzu GC-2010 Plus and HS-10 Headspace Sampler

Screening of pesticides in water using SPE on line

Preparative Separation of Active Components from Natural Products using Low-pressure Gradient Preparative HPLC

Rapid Screening and Confirmation of Melamine Residues in Milk and Its Products by Liquid Chromatography Tandem Mass Spectrometry

Highly sensitive quantitative analysis of Felodipine and Hydrochlorothiazide from plasma using LC/MS/MS

Determination of N-Nitrosamines by USEPA Method 521 using Triple Quadrupole Gas Chromatography Mass Spectrometry

Improved Automated Sample Preparation for the Analysis of 25-OH-Vitamin D3 by LC/MS/MS

Evaluation of a novel glass vial overcoming adsorption effect for pharmaceutical drugs

Determination of 198 pesticide residues in eggplant using Gas Chromatography tandem Mass Spectrometry/Mass Spectrometry

Highly sensitive and rapid analysis of synthetic dyes in sea food by LC/MS/MS

EPA Method 535: Detection of Degradates of Chloroacetanilides and other Acetamide Herbicides in Water by LC/MS/MS

High-Throughput LC-MS/MS Quantification of Estrone (E1) and Estradiol (E2) in Human Blood Plasma/Serum for Clinical Research Purposes

Maximizing Triple Quadrupole Mass Spectrometry Productivity with the Agilent StreamSelect LC/MS System

Plasma-free Metanephrines Quantitation with Automated Online Sample Preparation and a Liquid Chromatography-Tandem Mass Spectrometry Method

Fast and Reliable Method for the Analysis of Methylmalonic Acid from Human Plasma

Determination of VOCs by USEPA Method 8260 with Extended Dynamic Range using Fast, Sensitive Capillary GC/MS

Analysis of Illegal Dyes in Food Matrices using Automated Online Sample Preparation with LC/MS

A novel approach to the analysis of multivitamin by online supercritical fluid extraction/supercritical fluid chromatography

Macrolides in Honey Using Agilent Bond Elut Plexa SPE, Poroshell 120, and LC/MS/MS

Analysis of Synthetic Cannabinoids and Metabolites: Adding New Compounds to an Existing LC-MS/MS Method

Appendix II- Bioanalytical Method Development and Validation

A Method for Simultaneous Analysis of 174 Pesticides in Grape Using GC-MS/MS

Simultaneous determination of 74 kinds of pesticides in Chinese herbal medicine listed in Chinese pharmacopoeia (2015) by GPC-GC-MS/MS

Applying MRM Spectrum Mode and Library Searching for Enhanced Reporting Confidence in Routine Pesticide Residue Analysis

Research of Polychlorinated Biphenyls (PCBs) in Vegetables by GC-MS/MS

COMPREHENSIVE LC X LC ANALYSIS OF FLAVORING INGREDIENTS IN DISTILLED SPIRITS

Agilent 6460 Triple Quadrupole LC/MS System with an Agilent 1290 Infinity LC For Multi-Plant Growth Regulator Analysis in Grapes

Analysis of Pesticides in Baby Foods Using a Triple-Quadrupole GC/MS/MS

Analysis of Low-Calorie Sweeteners by Liquid Chromatography-Tandem Mass Spectrometry

EPA Method 535: Detection of Degradates of Chloroacetanilides and other Acetamide Herbicides in Water by LC/MS/MS

Extraction of Methylmalonic Acid from Serum Using ISOLUTE. SAX Prior to LC-MS/MS Analysis

Tecan AC Extraction Plate

Quantitative Analysis of Water-Soluble B-Vitamins in Cereal Using Rapid Resolution LC/MS/MS. Application. Authors. Abstract.

Analysis of Pesticides in Citrus Oil Using a Shimadzu GCMS-TQ8030. No. GCMS No. SSI-GCMS-1404

Consumables Guide for the Cannabis Testing Lab

Tomorrow s quantitation with the TSQ Fortis mass spectrometer: quantitation of phenylephrine hydrochloride for QA/QC laboratories

Development of 2D-LC/MS/MS Method for Quantitative Analysis of 1α,25-Dihydroxylvitamin D3 in Human Serum

Extraction of Cocaine and Metabolites From Urine Using ISOLUTE SLE+ prior to LC-MS/MS Analysis

Improved Extraction of THC and its Metabolites from Oral Fluid Using Oasis PRiME HLB Solid Phase Extraction (SPE) and a UPLC CORTECS C 18

Using UHPLC-Triple Quadrupole MS/MS to Detect the Presence of Bark Extract and Yohimbine Adulteration in Dietary Supplements and Botanicals

Extraction of Aflatoxins and Ochratoxin from Dried Chili Using ISOLUTE. Myco Prior to LC-MS/MS Analysis

Yun W. Alelyunas, Mark D. Wrona, Russell J. Mortishire-Smith, Nick Tomczyk, and Paul D. Rainville Waters Corporation, Milford, MA, USA INTRODUCTION

Analysis of Serum 17-Hydroxyprogesterone, Androstenedione, and Cortisol by UPLC-MS/MS for Clinical Research

A Sensitive and Reproducible Signature Peptide MRM Based Quantitation Method for Pegylated Interferon α-2b in Serum

Quantitative Determination of Dioxins in Drinking Water by Isotope Dilution using Triple Quadrupole GC-MS/MS

Fast and Accurate Analysis of Fluorotelomer Alcohols and Acrylates using Triple Quadrupole GC-MS/MS

LC-MS/MS Method for the Determination of Diclofenac in Human Plasma

Analysis of allergens found in cosmetics using MDGC-GCMS (Multi-Dimensional Gas Chromatograph Mass Spectrometer)

Application Note LCMS-110 Development of a Targeted Quantitative LC-MS/MS Method for 431 Positive and Negative Ion Pesticides in a Single Analysis

Determination of Hormones in Drinking Water by LC/MS/MS Using an Agilent InfinityLab Poroshell HPH Column (EPA 539)

Determination of Beta-Blockers in Urine Using Supercritical Fluid Chromatography and Mass Spectrometry

Quantitative Analysis of β-lactam Antibiotics in Human Plasma by High Sensitivity LC/MS/MS Method

LC-MS/MS Analysis of Phytocannabinoids and their

Structural Analysis by In-Depth Impurity Search Using MetID Solution and High Accuracy MS/MS

Analysis of Biomarkers in Crude Oil Using the Agilent 7200 GC/Q-TOF

Plasma Metanephrines and 3-Methoxytyramine by LC/MS/MS Using Agilent SimpliQ WCX SPE, 1290 Infi nity LC, and 6460 Triple Quadrupole LC/MS

Overview. Introduction. André Schreiber AB SCIEX Concord, Ontario (Canada)

Ultrafast Analysis of Buprenorphine and Norbuprenorphine in Urine Using the Agilent RapidFire High-Throughput Mass Spectrometry System

Chiral Separation Using SFC and HPLC

+ butanal + 2-picolineborane. + acetic acid. + butanal + 2-picolineborane. + acetic acid

Forensic and toxicological drug screening using liquid chromatography-tandem mass spectrometry with MS/MS library based identification

Identification and Quantitation of Pesticides in Chamomile and Ginger Extracts Using an Agilent 6460 Triple Quadrupole LC/MS system with Triggered MRM

Fast Screening and Quantitation of Perfluorinated Sources from Textiles using Chemical Ionization GC-MS

Clinical Toxicology. Biomass Component Extraction: The uneaten cooked plant specimen was prepared for

AB SCIEX SelexION Technology Used to Improve Mass Spectral Library Searching Scores by Removal of Isobaric Interferences

High Sensitivity HPLC Analysis of Perchlorate in Tap Water Using an Agilent 6460 Triple Quadrupole LC/MS System

LC/MS/MS qua ntitation of β-estradiol 17-acetate using an Agilent 6460 Triple Quadrupole LC/MS working in ESI negative ion mode

Evaluation of a New HPLC, a New Tandem MS and a New Data Processing Software for General Clinical Use

isobaric Barbiturates in Serum using LDTD- MS/MS combined with differential mobility

Pittcon P

Liquid Chromatography Mass Spectrometry. Shimadzu Corporation, UK; 2 Phytocontrol, France; 3 Shimadzu France, France. Trimesium S + CH 3 ETU

VOC Analysis of Water-Based Coatings by Headspace-Gas Chromatography

Supporting Information. Sweetened Swimming Pools and Hot Tubs

LC/MS/MS of Fungicides and Metabolites in Apple Juice with Agilent Bond Elut Plexa and Poroshell 120

Sensitive Detection of 2-MIB and Geosmin in Drinking Water

Rapid method development to study plasma stability of diverse pharmaceutical compounds using Rapid Resolution LC and triple quadrupole MS

LC/MS/MS of Fungicides and Metabolites in Orange Juice with Agilent Bond Elut Plexa and Poroshell 120

LC/MS/MS Analysis of Pesticide Residues in Apples Using Agilent Chem Elut Cartridges

Quantitative analysis of small molecules in biological samples. Jeevan Prasain, Ph.D. Department of Pharmacology & Toxicology, UAB.

Analysis of Stachydrine in Leonurus japonicus Using an Agilent ZORBAX RRHD HILIC Plus Column with LC/ELSD and LC/MS/MS

Fast and Accurate Quantitation of Perfluorinated Sources from Textiles using Gas Chromatography-Triple Quadrupole Mass Spectrometry

Determination of Organochlorine Pesticides and Polychlorinated Biphenyls Using GC/MS/MS Operated in the MRM Mode

Multiple Fragmentation Methods for Small Molecule Characterization on a Dual Pressure Linear Ion Trap Orbitrap Hybrid Mass Spectrometer

The Quantitation and Identification of Coccidiostats in Food by LC-MS/MS using the AB SCIEX 4000 Q TRAP System

Analysis of Cannabinoids and Amphetamines in Serum by RRLC/Triple Quadrupole Mass Spectrometry Using a Multimode Ion Source. Application.

Accurate Mass Analysis of Hydraulic Fracturing Waters: Identification of Polyethylene Glycol Surfactants by LC/Q-TOF-MS

Validation Report 18

High-Throughput Protein Quantitation Using Multiple Reaction Monitoring

Transcription:

Liquid Chromatography Mass Spectrometry SSI-LCMS-096 Quantitation of Ethyl Glucuronide and Ethyl Sulfate in Urine using LC-MS/MS LCMS-8045 Summary: A short, robust quantitative method for the analysis of ethyl glucuronide (EtG) and ethyl sulfate () using a Nexera LC coupled to LCMS-8045 triple quadrupole mass spectrometer was developed. Background: EtG and are metabolites of ethanol that are used to measure alcohol use. These metabolites are important to measure for zero tolerance treatment programs and rehab facilities. Method: EtG and standards and deuterated internal standards were purchased from Restek Corporation (Bellefonte, PA). A working internal standard (IS) of 100 ng/ml of EtG-d5 and -d5 was prepared in 0.1% formic acid as the dilution solvent. Working solutions of EtG and were prepared at 50, 100, 200, 500, 1000, 2500, and 5000 ng/ml in both pooled urine and synthetic urine (surine). In addition, four QC working solutions were prepared at 50 (LLOQ), 125 (LQC), 700 (MQC), and 4000 (HQC) ng/ml in both pooled urine and surine. The calibration and QC standards were prepared by aliquoting 50 µl of each working solution and diluting with 950 µl with working IS solution to yield a total of seven calibrators and 4 QC samples for both pooled urine and surine. The standards were vortexed and centrifuged for 10 minutes at 4000 rpm and the supernatant was injected onto the LCMS-8045. The structures for EtG and are shown in Figure 1. Figure 1. Chemical structures for ethyl sulfate () and ethyl glucuronide (EtG)

A Raptor EtG/ column from Restek (100 x 2.1mm, 2.7µm) was used with an UltraShield UHPLC precolumn filter (0.2 µm frit) and a linear binary gradient consisting of 0.1% formic acid in water and 0.1% formic acid in acetonitrile. The gradient conditions are shown in Table 1. The column oven was at 0 C and the injection volume was 10 µl. Time (min) %B 1 5 5 1 5 4 stop Table 1. LC gradient conditions. Negative mode electrospray ionization with multiple reaction monitoring (MRM) transitions were used for analysis on the LCMS-8045. The MRM transitions for each analyte and internal standard are shown in Table 2. Analyte MRM Transition CE (V) 125.1>97.10 17 125.1>80 0 d5 10.1>98.05 19 221.2>75.10 15 EtG 221.2>80 17 EtG d5 226.2>80 17 Table 2. MRM transitions for EtG, EtG-d5,, -d5. 2.75 2 0 0 0 1 0 0 0 0 0 0 0 2.75.00.25 0.75 min Figure 2. Chromatogram of double blank urine. Peak 1 and 2 show matrix interference peaks. 2.2 2.1 (x100) 1.9 1.8 1.7 1.6 1.4 1. 1.2 1.1 0.9 0.8 0.7 0.6 0.4 0. 0.2 0.1-0.1 0 0 0 0 0 2.75.00.25 0.75 min Figure. Chromatogram of double blank synthetic urine (surine). Results and Discussion: In order to ensure that there were no interference peaks in matrix, a double blank of both urine and surine samples was run (Figures 2 and ). The double blank has two known matrix peaks at min and 1.2 min as shown. The surine sample did not show any matrix peaks. EtG elutes at 0.81 min and elutes at 1.87 min which is baseline resolved from the matrix peaks.

This is shown in the chromatograms in Figure 4 and 5 for the 100 ng/ml samples. The calibration curves for EtG and in urine are shown in Figures 6 and 7, respectively. The green points represent the QC samples and red points are the calibration points. The accuracy for each QC ranged from 88-114% for EtG and 95-98% in in the urine samples. For the surine samples, calibration curves are shown in Figures 8 and 9. The accuracy ranged from 88-99% for EtG and 91-102% for. Tables and 4 show the results for each calibration curve. 7.5 (x10,000) 7.0 6.5 6.0 5.5.0 1 EtG 0 0 0 0 0 2.75.00.25 0.75 min Figure 4. 100 ng/ml standard of EtG/ in Pooled Urine. EtG (peak 2), (peak 4). 0 (x10,000) 4.25 0.75 0.25.00 2.75 0 0 EtG 0 0 0 0 0 0 0 0 2.75.00.25 0.75 min Figure 5. 100 ng/ml standard of EtG/ in Surine. EtG (peak 2), (peak 4).

Area Ratio AreaRatio y = 00524099x - 04797849 R² = 0.998178.0 0 250 500 750 100012501500175020002250250027500002505007504000425045004750 Conc.Ratio Figure 6. Calibration curve for EtG in urine. Red points are calibration points, Green points are QC samples. 0 0 0 0 y = 00498579x + 055796 R² = 0.999298 0 0 250 500 750 100012501500175020002250250027500002505007504000425045004750 Conc.Ratio Figure 7. Calibration curve for in urine. Red points are calibration points, Green points are QC samples. QC Spiked EtG/ Avg. EtG in Urine % Accuracy Avg. in Urine % Accuracy LLOQ LQC MQC HQC 50ng/mL 125ng/mL 700ng/mL 4000ng/mL 44.27 88.5 47.67 95.5 142.81 114.25 12.0 98.4 745.8 106.55 675.64 96.52 691.14 92.28 855.76 96.9 Table. Average calculated levels of EtG and and %Accuracy for LLOQ, LQC, MQC and HQC samples in urine.

AeaRatio.0 y = 004495269x - 02028566 R² = 0.9984420 0 250 500 750 100012501500175020002250250027500002505007504000425045004750 Conc.Ratio Figure 8. Calibration curve for EtG in surine. AreaRatio 2.4 y = 00494269x + 0447814 2.2 R² = 0.999477 1.8 1.6 1.4 1.2 0.8 0.6 0.4 0.2 0 250 500 750 1000 1250 1500 1750 2000 2250 2500 2750 000 250 500 750 4000 4250 4500 4750 Conc.Ratio Figure 9. Calibration curve for in surine. QC Spiked EtG/ Avg. EtG in Surine % Accuracy Avg. in Surine % Accuracy LLOQ LQC MQC HQC 50ng/mL 125ng/mL 700ng/mL 4000ng/mL 4 88.1 45.9 91.8 119.6 95.7 12.9 99.1 670.4 95.8 716.4 102. 95.1 98.8 4066.5 101.7 Table 4. Average calculated levels of EtG and and %Accuracy for LLOQ, LQC, MQC and HQC samples in surine.

In addition to running calibration standards, two UTAK controls (level 1 and level 2) and two positive in-house urine samples (56045 and 5604) were analyzed with this method. The chromatograms for the UTAK controls are shown in Figures 10 and 11 and the in-house positive samples are shown in Figures 12 and 1. The calculated concentrations for the UTAK standards are listed in Table 5. The calculated concentrations for the in house positive samples are listed in Table 6.One can clearly see that the matrix effects are fully resolved from the analyte peaks and the amount found in each sample can be easily quantified using the calibrations. 0 (x10,000) 4.75 0 4.25 0.75 0.25.00 2.75 0 0 0 0 1 EtG UTAK LEVEL 1 EtG/ urine 0-0 0 0 0 0 2.75.00.25 0.75 min Figure 10. Chromatogram for UTAK Level 1 standard. Peaks 1 and are matrix peaks. 4.25 (x10,000) 0.75 0.25.00 2.75 0 0 0 0 1 EtG UTAK LEVEL 2 EtG/ urine 0 0 0 0 0 0 2.75.00.25 0.75 min Figure 11. Chromatogram for UTAK Level 2 standard. Peaks 1 and are matrix peaks. Level 1 Level 2 Target Value Reference Value Target Value Reference Value EtG 500ng/mL 481 ng/ml 2000 ng/ml 1870 ng/ml 200ng/mL 199 ng/ml 800 ng/ml 75ng/mL Table 5. Calculated reference values for UTAK samples for EtG and.

(x10,000) 5.5.0 1 EtG 56045 0 0 0 0 0 2.75.00.25 0.75 min Figure 12. Chromatogram for 56045 positive in-house sample. Peaks 1 and are matrix peaks. 6.0 (x10,000) 5.5 5604.0 EtG 1 0 0 0 0 0 2.75.00.25 0.75 min Figure 1. Chromatogram for 5604 positive in-house sample. Peaks 1 and are matrix peaks. Sample ID Mean EtG Conc in Urine. ng/ml Mean Conc in Urine. ng/ml 56045 1461. 84 5604 2275.4 1152.2 Table 6. Calculated values for positive in-house samples for EtG and. Conclusion: An rapid, accurate and robust method was developed using the LCMS-8045 triple quadrupole mass spectrometer to measure EtG and in urine and surine samples. The accuracy values were all between 82-116% and the calibrations were able to successfully measure EtG and in unknown samples. The ability to be able to fully resolve the urine matrix peaks from EtG and allows for a simple and quantifiable method for analyzing these two biomarkers. Acknowledgements: We would to thank Restek Corporation for their assistance with providing the standards, column and results for this application note.

Consumables used in this application Part Number REST-925A12 REST-25809 REST-4101 REST-4102 REST-410 REST-4104 Description Raptor EtG/. 2.7 µm x 100 x 2.1 mm UltraShield UHPLC precolumn filter, 0.2 µm frit Ethyl-β-D-glucuronide (EtG) Ethyl-β-D-glucuronide-d5 (EtG-d5) Ethyl Sulfate sodium salt () Ethyl Sulfate-d5 sodium salt (-d5) 220-91545-49 0.1% Formic acid in water (1L) 220-91545-47 0.1% Formic acid in acetonitrile (1L) 220-4001-01 Vials, LC, LabTotalKit, 100/pk 220-9129-40 220-9129-41 EtG/ Analysis Startup Kit RUO Reference Material Version EtG/ Analysis Startup Kit RUO Certified Reference Material Version

LCMS-8040 LCMS-8045 LCMS-8050 LCMS-8060 LCMS-2020 LCMS-IT-TOF Founded in 1875, Shimadzu Corporation, a leader in the development of advanced technologies, has a distinguished history of innovation built on the foundation of contributing to society through science and technology. Established in 1975, Shimadzu Scientific Instruments (SSI), the American subsidiary of Shimadzu Corporation, provides a comprehensive range of analytical solutions to laboratories throughout North, Central, and parts of South America. SSI maintains a network of nine regional offices strategically located across the United States, with experienced technical specialists, service and sales engineers situated throughout the country, as well as applications laboratories on both coasts. For information about Shimadzu Scientific Instruments and to contact your local office, please visit our Web site at www.ssi.shimadzu.com Shimadzu Corporation www.shimadzu.com/an/ SHIMADZU SCIENTIFIC INSTRUMENTS, INC. Applications Laboratory 7102 Riverwood Drive, Columbia, MD 21045 Phone: 800 477 1227 Fax: 410 81 1222 URL http://www.ssi.shimadzu.com For Research Use Only. Not for use in diagnostic procedures.the content of this publication shall not be reproduced, altered or sold for any commercial purpose without the written approval of Shimadzu.The information contained herein is provided to you as is without warranty of any kind including without limitation warranties as to is accuracy or completeness. Shimadzu does not assume any responsibility or liability for any damage, whether direct or indirect, relating to the use of this publication.this publications is based upon the information available to Shimadzu on or before the date of publication, and subject to change without notice. Shimadzu Scientific Instruments, 2018 First Edition: February 2018