Simultaneous Qualitative and Quantitative Data Acquisition for Research of Diabetes Drugs



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

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

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

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

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

Overview. Introduction. AB SCIEX MPX -2 High Throughput TripleTOF 4600 LC/MS/MS System

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

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

Thermo Scientific Prelude SPLC System FPO. Making LC/MS accessible. to clinical research and toxicology labs

Ultra Fast UHPLC-LCMSMS Method Development in Clinical Drug Monitoring

MultiQuant Software 2.0 for Targeted Protein / Peptide Quantification

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

Increasing the Multiplexing of High Resolution Targeted Peptide Quantification Assays

MultiQuant Software Version 3.0 for Accurate Quantification of Clinical Research and Forensic Samples

Overview. Purpose. Methods. Results

Simultaneous qualitative and quantitative analysis using the Agilent 6540 Accurate-Mass Q-TOF

Introduction. Methods. Sample Processing

Accurate Mass Screening Workflows for the Analysis of Novel Psychoactive Substances

HRMS in Clinical Research: from Targeted Quantification to Metabolomics

Analysis of Organophosphorus Pesticides in Milk Using SPME and GC-MS/MS. No. GCMS No. SSI-GCMS Shilpi Chopra, Ph.D.

The Use of Micro Flow LC Coupled to MS/MS in Veterinary Drug Residue Analysis

API 3200 LC/MS/MS SYSTEM. Performance, productivity and value combined

Therapeutic Drug Monitoring of Antiretroviral Drugs with HPLC-MS

Cliquid Drug Screen & Quant Software for Routine Forensic Toxicology. great interest in forensic, toxicological and clinical research laboratories.

A High Throughput Automated Sample Preparation and Analysis Workflow for Comprehensive Forensic Toxicology Screening using LC/MS/MS

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

In-Depth Qualitative Analysis of Complex Proteomic Samples Using High Quality MS/MS at Fast Acquisition Rates

Simultaneous Quantitation of 43 Drugs in Human Urine with a Dilute-and-Shoot LC-MS/MS Method

LC-MS/MS for Chromatographers

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

Sensitive steroid analysis on a new High Speed Triple Quadrupole LC/MS/MS. Mikaël LEVI Shimadzu France

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

SIMULTANEOUS DETERMINATION OF NALTREXONE AND 6- -NALTREXOL IN SERUM BY HPLC

Jennifer L. Simeone and Paul D. Rainville Waters Corporation, Milford, MA, USA A P P L I C AT ION B E N E F I T S INT RO DU C T ION

NANOCOMPOSIX'S GUIDE TO ICP-MS MEASUREMENT

DRUG METABOLISM. Drug discovery & development solutions FOR DRUG METABOLISM

A Generic LC-MS Method for the Analysis of Multiple of Drug of Abuse Classes with the Thermo Scientific Exactive TM System

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

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

Metabolomic Profiling of Accurate Mass LC-MS/MS Data to Identify Unexpected Environmental Pollutants

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

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

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

S olid Ph ase Extraction (SP E) Method:

Method Development of LC-MS/MS Analysis of Aminoglycoside Drugs: Challenges and Solutions

High Sensitivity MS Determination of Carryover in a New Autosampler Design

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

Waters Core Chromatography Training (2 Days)

The Scheduled MRM Algorithm Enables Intelligent Use of Retention Time During Multiple Reaction Monitoring

Improving the Metabolite Identification Process with Efficiency and Speed: LightSight Software for Metabolite Identification

EKSIGENT EKSPERT NANOLC 400. Unmatched flexibility for low flow LC/MS

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

Utilization of Rapid LC-MS for Screening and Quantitative Analysis of Pesticides in Food Matrix using an Exactive Plus Benchtop Orbitrap Platform

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

Unique Software Tools to Enable Quick Screening and Identification of Residues and Contaminants in Food Samples using Accurate Mass LC-MS/MS

VALIDATION OF ANALYTICAL PROCEDURES: TEXT AND METHODOLOGY Q2(R1)

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

Guidance for Industry

UPLC-MS/MS Analysis of Aldosterone in Plasma for Clinical Research

Multi Pesticides Residue analysis in Ayurvedic cough Syrup by GCMS/MS using QuEChERS extraction method

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

RAPID MARKER IDENTIFICATION AND CHARACTERISATION OF ESSENTIAL OILS USING A CHEMOMETRIC APROACH

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

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

Development and Validation of a LC-MS/MS Method for Plasma Analysis of the Serotonin Metabolite: 5-Hydroxyindoleacetic acid (5-HIAA)

Quick and Sensitive Analysis of Multiclass Veterinary Drug Residues in Meat, Plasma, and Milk on a Q Exactive Focus LC-MS System

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

Innovative vs Traditional

How To Test For Contamination In Large Volume Water

CORESTA RECOMMENDED METHOD N 72

Determination of Food Dye Concentrations in an Unknown Aqueous Sample Using HPLC

Agilent Enhanced Matrix Removal Lipid LOSE THE LIPIDS, FIND YOUR ANALYTES

A feasibility study of the determination of B-group vitamins in food by HPLC with Mass Spectrometric detection. LGC/R/2011/181 LGC Limited 2011

Thermo Scientific Mass Spectrometric Immunoassay (MSIA)

A Generic Kit-Based Approach for Quantifying Monoclonal Antibody Drugs Through Direct Digestion of Discovery Study Samples

METHOD OF ANALYSIS. N methyl 2-pyrrolidone

How To Develop A Recipe Card

A New QuEChERS Dispersive SPE Material and Method for Analysis of Veterinary Drug Residue by LC-MS-MS

Rapid and Reproducible Amino Acid Analysis of Physiological Fluids for Clinical Research Using LC/MS/MS with the atraq Kit

A Novel Approach to Low Volume Sample Preparation

Making the Leap to LC/MS/MS: Enhancing and Accelerating Clinical Research and Forensic Toxicology Applications

NUVISAN Pharma Services

Application Note # LCMS-92 Interlaboratory Tests Demonstrate the Robustness and Transferability of the Toxtyper Workflow

8. SUMMARY AND CONCLUSION

Extraction of Cannabinoids in Marijuana and Edibles by QuEChERS

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

CONFIRMATION OF ZOLPIDEM BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY

Investigating Biological Variation of Liver Enzymes in Human Hepatocytes

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

Pesticide Analysis by Mass Spectrometry

Analysis of Various Vitamins in Multivitamin Tablets

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

Multifunctional Autosampler AOC-6000 C146-E272A

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

Application Note # LCMS-62 Walk-Up Ion Trap Mass Spectrometer System in a Multi-User Environment Using Compass OpenAccess Software

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

Transcription:

Liquid Chromatography Mass Spectrometry SSI-LCMS-068 Simultaneous Qualitative and Quantitative Data Acquisition for Research of Diabetes Drugs LCMS-8050 Summary By utilizing the LCMS-8050 s ultrafast scan speed, both quantitative and qualitative data were acquired for 5 drugs simultaneously without the need for an ion trap. Background Diabetes has an impact on the lives of a large number of people worldwide and thus has generated a need for high quality data for research. As the need for more data coincides with ever increasing laboratory costs, the ability to efficiently extract data has become more important than ever. The speed of the LCMS-8050 allows for quantitative data to be acquired while also simultaneously acquiring qualitative scans that can be used for further confirmation or to further research. ere we acquire product ion scans during MRM acquisition to add an additional layer of confirmation. This can then be compared to a library search or visual examination. Method To a 100 ul aliquot of plasma, 300 µl acetonitrile was added. Samples were then centrifuged and 100 µl of the supernatant diluted with 200 µl of Mobile Phase A. 7 µl was injected onto an LCMS-8050 with a exera LC system. Analytes were separated using a Raptor ARC C18 column (2.0 x 50-2.7 µm particle) from Restek. All analytes were separated in 1.7 minutes. 2 Metformin Canagliflozin S 2 Sitagliptin igure 1. Chemical structures for the compounds analyzed. S Glimepiride ateglinide 1

900000 Sitigliptin 800000 700000 600000 500000 400000 300000 Metformin Glimepiride ateglinide 200000 100000 0 Canagliflozin 0.25 0.50 0.75 1.00 1.25 1.50 1.75 min igure 2. Example chromatogram of all 5 drugs in human plasma. 17.5 10.0 15.0 R 2 =0.995 R 2 =0.999 12.5 10.0 7.5 7.5 5.0 2.5 0.0 0 250 500 750 Conc. Ratio 5.0 2.5 0.0 0.45 0.40 0.35 0.30 0.25 0.20 0.15 0.10 0.05 9 R 2 =0.994 8 R 2 =0.997 7 6 5 4 3 2 1 0.00 0 9 8 7 6 5 4 3 2 1 R 2 =0.996 0 igure 3. Calibration curves for each drug in human plasma. 2

ame Metformin Sitigliptin Canagliflozin Glimepiride ateglinide Matrix Concentration (ng/ml) Calculated. Con. (ng/ml) %CV Accuracy 25 28.4 0.3 113.6 75 68.4 2.5 91.2 750 785.8 1.1 104.8 25 24.8 5.3 99.2 75 73.7 1.9 98.3 750 718.4 4.6 95.8 3 2.9 1.9 96.7 75 74.5 0.5 99.3 750 744.9 1.3 99.3 3 3.1 1.6 103.3 75 72.2 0.9 96.3 750 709.3 1.7 94.6 25 24.1 12.5 96.4 75 76.6 7.8 102.1 750 829.8 4.8 110.6 25 27.2 1.0 108.8 75 77.6 3.8 103.5 750 734.1 3.8 97.9 3 3.3 3.0 110.0 75 76.4 0.3 101.9 750 766.3 4.4 102.2 25 24.9 5.2 99.6 75 72.6 9.1 96.8 750 739.0 2.7 98.5 25 24.9 5.2 99.6 75 72.6 9.1 96.8 750 739 2.7 98.5 3 3.0 4.4 100.0 75 74.9 1.4 99.9 750 736.5 0.3 98.2 Table 1. Quality control samples at 3 different levels (n=3) for all 5 analytes in both human and mouse plasma. 3

5.0 Inten.(x100,000) 174 193 4.0 3.0 2.0 154 1.0 56 127 235 0.0 50 100 150 200 250 300 350 400 m/z igure 4. A. Perform library search based on product ions. B. View qualitative results while analyzing quantitative data. 4

igure 5. Product ion scans are easily built into the same acquisition method as MRM transitions. Results and Discussion Data was acquired simultaneously for 5 diabetic drugs in both a qualitative and quantitative manner. With an acquisition time of under 1.7 minutes, it allows an enormous amount of information to be generated in a short period of time increasing a laboratory s capabilities and reducing cost. The LCMS-8050 s unrivaled scan speed and sensitivity allows for consistent, robust, and accurate high throughput analysis in complex matrices. igure 1. shows the chemical structures for each analyte. igure 2. shows representative chromatograms of all analytes and their reference ions. As demonstrated in igure 3. and Table 1., excellent linearity and accuracy was achieved. The accuracy of the quality controls samples was always within 15% and R2 values for all curves was >0.990. In addition to accuracy, precision remained strong even with the ultra high scan speeds. Conclusion The accurate and sensitive detection of 5 diabetes drugs in under 1.7 minutes was accomplished using an LCMS-8050 in conjunction with fast chromatography. In addition, the simultaneous acquisition of product ion scans shows qualitative work flows can be executed at the same time quantitative analysis is being done. 5

LCMS-8030 LCMS-8040 LCMS-8050 LCMS-2020 LCMS-IT-T ounded 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 orth, 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. or 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/ SIMADZU SCIETIIC ISTRUMETS, IC. Applications Laboratory 7102 Riverwood Drive, Columbia, MD 21045 Phone: 800-477-1227 ax: 410-381-1222 URL http://www.ssi.shimadzu.com or Research Use nly. ot 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, 2012 irst Edition: ctober, 2012