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



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

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

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

Discovery of Pesticide Protomers Using Routine Ion Mobility Screening

Analysis of Fat-Soluble Vitamin Capsules using UltraPerformance Convergence Chromatography (UPC 2 )

Henry Shion, Robert Birdsall, Steve Cubbedge, and Weibin Chen Waters Corporation, Milford, MA, USA APPLICATION BENEFITS INTRODUCTION WATERS SOLUTIONS

Eleanor Riches Waters Corporation, Manchester, UK INTRODUCTION

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

WATERS QUANTITATIVE ANALYSIS solutions

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

Salman Azimi, 1 Nayan S. Mistry, 2 and Michelle Wood 2. Drug Quality Control Laboratory, Supreme Council of Health, Doha, Qatar 2

Robert Birdsall, Eoin Cosgrave, Henry Shion, and Weibin Chen Waters Corporation, Milford, MA, USA APPLICATION BENEFITS INTRODUCTION WATERS SOLUTIONS

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

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

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

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

Waters Core Chromatography Training (2 Days)

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

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

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

Method Development for Size-Exclusion Chromatography of Monoclonal Antibodies and Higher Order Aggregates

Hydrophilic-Interaction Chromatography (HILIC) for LC-MS/MS Analysis of Monoamine Neurotransmitters using XBridge BEH Amide XP Columns

Analysis of Vegetable Oils by High Performance Liquid Chromatography

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

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

MEDICINAL CHEMISTRY APPLICATIONS BOOK

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

Accurate Mass Screening Workflows for the Analysis of Novel Psychoactive Substances

How To Use An Acquity Qda Detector

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

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

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

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

NUVISAN Pharma Services

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

Pesticide Analysis by Mass Spectrometry

Vitamin C quantification using reversed-phase ion-pairing HPLC

Increasing the Multiplexing of High Resolution Targeted Peptide Quantification Assays

Simultaneous Qualitative and Quantitative Data Acquisition for Research of Diabetes Drugs

Chemical analysis service, Turner s Green Technology Group

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

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

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

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

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

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

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

CONFIRMATION OF ZOLPIDEM BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY

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

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

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

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

ApplicationNOTE Introduction

AxION edoor. Web-Based, Open-Access Mass Spectrometry Software

PosterREPRINT AN LC/MS ORTHOGONAL TOF (TIME OF FLIGHT) MASS SPECTROMETER WITH INCREASED TRANSMISSION, RESOLUTION, AND DYNAMIC RANGE OVERVIEW

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

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

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

Effects of Intelligent Data Acquisition and Fast Laser Speed on Analysis of Complex Protein Digests

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

Reversed Phase High Presssure Liquid Chromatograhphic Technique for Determination of Sodium Alginate from Oral Suspension

DEVELOPMENT OF PFCs HIGH SENSITIVITY ANALYSIS METHOD APPLIED RETENTION GAP TECHNIQUE WITH UPLC/MS/MS

AMD Analysis & Technology AG

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

MultiQuant Software 2.0 for Targeted Protein / Peptide Quantification

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

[ DISQUE DISPERSIVE SAMPLE PREPARATION EXTRACTION PRODUCTS ] QuEChERS. Simplifed

Determination of Caffeine in Beverages HPLC-1

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

Micromass LCT User s Guide

Project 5: Scoville Heat Value of Foods HPLC Analysis of Capsaicinoids

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

Fast and Automatic Mapping of Disulfide Bonds in a Monoclonal Antibody using SYNAPT G2 HDMS and BiopharmaLynx 1.3

Analyzing Small Molecules by EI and GC-MS. July 2014

HPLC Analysis of Acetaminophen Tablets with Waters Alliance and Agilent Supplies

Overview. Purpose. Methods. Results

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

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

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

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

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

INTEGRATED TECHNOLOGY TO SEE THE WHOLE PICTURE. AxION iqt GC/MS/MS

SIMULTANEOUS QUANTITATIVE DETERMINATION OF OPIOID DEPENDENCY TREATMENT DRUGS IN HUMAN URINE USING UPLC/MS/MS

Guide to Reverse Phase SpinColumns Chromatography for Sample Prep

LC-MS/MS for Chromatographers

DRUG METABOLISM. Drug discovery & development solutions FOR DRUG METABOLISM

How To Develop A Recipe Card

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

Background Information

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

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

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

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

HRMS in Clinical Research: from Targeted Quantification to Metabolomics

How To Test For Contamination In Large Volume Water

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

AMINO ACID ANALYSIS By High Performance Capillary Electrophoresis

Appendix 5 Overview of requirements in English

Transcription:

Analysis of Polyphenols in Fruit Juices Using ACQUITY UPLC H-Class with UV and MS Detection Evelyn Goh, Antonietta Gledhill Waters Pacific, Singapore, Waters Corporation, Manchester, UK A P P L I C AT ION B E N E F I T S Rapidly separate, detect, identify, and quantify polyphenolic compounds in fruit juices. Reduces analysis time from over an hour with HPLC methods to under 0 minutes using ACQUITY UPLC, increasing sample throughput for juice QC labs along with improved chromatographic performance. GOA L To detect, confirm, and quantify polyphenolic compounds in fruit juices. INT RO DU C T ION Polyphenols are widely recognized as functional components of food and beverage products, such as tea, wine, and fruits. Polyphenols are reported to play a potential role in protecting human health from degenerative and cardiovascular diseases.,, Allows easy access to UV and mass spectral information for analytical labs performing quantification, data interpretation, and compound identification. Over the years, the determination of natural phenolic compounds has proved an extremely difficult analytical challenge, which has been hindered by the complexity of the numerous chemical classes and species, combined with inherent limitations of conventional HPLC separation methods. Typical HPLC methods that are used to separate and identify polyphenolic compounds by reversed phase chromatography often take more than an hour for a single run. More recently, analysis methods of polyphenols using Waters ACQUITY UPLC System have been developed, which provide increased resolution and shortened analysis times.,, The reduction in run time enables an increase in sample throughput, which is crucial for juice QC laboratories to deliver their products to store shelves more quickly. WAT E R S SO LU T IONS ACQUITY UPLC H-Class System ACQUITY UPLC PDA Detector ACQUITY SQ Detector Empower Software Waters ACQUITY UPLC H-Class System enables routine HPLC users to move to UPLC Technology easily by combining the speed and performance of UPLC with the ability to run HPLC separations. The use of the ACQUITY H-Class with UV and mass spectrometry provides a robust solution for the QC analysis of juice samples. In this application note, a rapid method for the detection and confirmation of polyphenolic compounds in fruit juices using the ACQUITY UPLC H-Class System is described. With the selectivity of the MS from the ACQUITY SQ Detector, analysis times can be further reduced for quantification of key components. K E Y W O R D S Polyphenols, fruit juices, quality control, QC

E X P E R IM E N TA L Materials Seven commercially available fruit juice samples, together with polyphenol standards were analyzed. Sample preparation Each juice sample was filtered through a 0. µm filter and diluted with an equal amount of water. Acquisition and processing methods Two methods were developed for the analysis of polyphenols on the ACQUITY UPLC H-Class System. Method is ideal for chromatographic fingerprinting, offering increased separation resolution resulting from a longer column. For QC laboratories performing routine quantification of the key phenolic compounds present, Method would be the preferred method, utilizing a shorter run time, thereby improving lab productivity. Method Column: ACQUITY UPLC HSS T. x 00 mm,.8 µm LC conditions LC system: Mobile phase A: ACQUITY UPLC H-Class Water + 0.% acetic acid Column temp: C Flow rate: 0. ml/min Total run time:.0 min Mobile phase B: Acetonitrile + 0.% acetic acid MS conditions MS System: ACQUITY SQ Detector Ionization: Electrospray Capillary voltage:.0 kv Sampling cone: 0 V Extraction cone:.0 V Source temp.: 0 C Desolvation temp.: 00 C Desolvation gas: 000 L/hr Cone gas: 0 L/hr Scan mass range: 0 to 0 m/z ACQUITY UPLC PDA conditions UV range: 0 to 00 nm (Extracted at 80 and 0 nm) Sampling rate: 0 pts/sec Filter time constant: Fast Time (min) %A %B Initial 99.0 99 0.0 0 0.0 9. 99.0 99 Method Column: ACQUITY UPLC HSS T. x 0 mm,.8 µm Column temp.: C Flow rate: 0.80 ml/min Total run time:.0 min Time (min) %A %B Initial 99 0. 99.0 0 0. 9. 99.0 99 All data were acquired and processed using Empower Software.

IntelliStart Software was used to automatically develop SIR acquisition methods for the phenolic compounds targeted in this analysis. IntelliStart requires only the entry of basic compound information; then it automatically locates the precursor ion and optimizes the cone voltage, as shown in Table. The dwell times were optimized to give a minimum of points across each chromatographic peak for reproducible quantitation. Quantitation of the juice samples was performed by calculating against a calibration curve for each of the polyphenol analytes in solution. Figure shows a typical MS method setup in Empower Software. Figure. MS method setup in Empower Software. Compound m/z Polarity Cone voltage (V) Arbutin. 0 Gallic acid 9. 0 -hydroxymethyl-- furaldehyde (HMF) Table. MS analysis parameters.. + 0 Chlorogenic acid. Catechin 89. 0 Caffeic acid 9. 0 Epicatechin 89. p-coumaric acid. Ferulic acid 9. 0 Phloridzin. 0 t-cinnamic acid.

R E SU LT S A N D D IS C U S S ION Using the ACQUITY UPLC H-Class System coupled with ACQUITY UPLC PDA and ACQUITY SQ detectors, polyphenol standards were separated and analyzed in 0 minutes, as shown in Figure. The PDA result was extracted at wavelengths 80 nm, shown in Figure, and 0 nm (data not shown), and SIR chromatograms for the analytes were overlaid, as shown in Figure..x0.x0.0x0 8.0x0.0x0.0x0.0x0 MS (SIR).9.8.8.00.80..0 8 9.0. 0 8. 9. 0.0.00.00.00.00.00.00.00 8.00 9.00 0.0 0. 0.0 PDA (80nm) Arbutin -.98 Gallic Acid -.0 HMF -. Chlorogenic Acid -.8 Catechin -.8 Caffeic Acid -.90 Epicatechin -. 8 p-coumaric Acid -.980 9 Ferulic Acid -.90 0 Phloridzin - 8.9 t-cinnamic Acid - 9..00.00.00.00.00.00.00 8.00 9.00 Figure. Simultaneous acquisition of PDA and MS (SIR) data for a 0 ppm standard mix in a single analysis. The retention times (Method and Method ) of the polyphenolic compound standards, along with their retention times and peak area %RSDs (based on six replicate injections) for MS detection using Method are shown in Table. Retention times (min) % RSD for Method (MS) Peak Compound Method Method Retention time Peak area Arbutin.0 0. 0. Gallic acid.0 0. 0.0 0.0 -hydroxymethyl--furaldehyde (HMF).8. 0.9 0. Chlorogenic acid.9. 0.9 0. Catechin.. 0.9 0. Caffeic acid.9. 0. 0. Epicatechin.. 0. 0. 8 p-coumaric acid.98.9 0.0 0. 9 Ferulic acid.9.8 0. 0. 0 Phloridzin 8.0.9 0. 0.8 t-cinnamic acid 9..8 0. 0. Table. Retention times and repeatability results.

A variety of commercially available fruit juices, namely apple, orange, berry, guava, mango, and lime were analyzed for their polyphenolic content. Both UV and MS data were simultaneously acquired. An example of the results from an apple juice sample analyzed using Method is shown in Figure. x0 x0 x0 SIR (HMF) SIR (Chlorogenic acid) SIR (Catechin) SIR (Caffeic acid) MS (SIR) 0.00.00.00.00.00.00 0. 0.08.9 PDA (80 nm) 0.0 0.0 0.0.8.898.9..00.00.00.00.00.00 Figure. Overlay of UV and MS chromatograms of polyphenol analysis in apple juice. By examining the PDA chromatogram in Figure, the polyphenol compounds present in apple juice can be easily assigned and identified by Empower Software.

To increase confidence in component identification beyond simple retention time matching, UV spectral library functions with PDA and Empower Software can be employed. Using HMF (Peak ) to illustrate, Figure shows the spectrum index plot for HMF standard, and the peak detected at the same retention time in apple juice. The spectral match between the HMF standard and Peak in apple juice confirms the identity of HMF in the apple juice..8 Extracted 8.0 0.00 0.00 Apple Juice 0.00. 8. 0 0 nm.8 Wavelength 0. 0.0 0.0 0. HMF Standard. Extracted 8.0 0.0 0 nm. Wavelength 0.00 0.0 0.0..0..0..80.8 Time.0..0..0..80.8 Time 0.08 0.0 0.0 0.0 PDA (80 nm) HMF -.8 Chlorogenic Acid -.9 Catechin -.898 Caffeic Acid -.9 Epicatechin -. Apple Juice.00.00.00.00.00.00 Figure. Spectrum index plot confirming the identity of HMF in apple juice.

With the additional coupling of a more selective detector, such as the ACQUITY SQ Detector, more information can be obtained in a single sample injection. This provides QC analysts with increased confidence in data interpretation and compound confirmation. From Figure, the HMF peak (Peak ) detected with MS further confirms the polyphenol identity in the juice. A closer look at the apple juice results in Figure revealed differences in the UV and MS chromatograms. SIR (Chlorogenic acid) SIR (Catechin) Catechin (Peak ) identified in UV is not detected in MS MS SIR (Caffeic acid) x0 x0 x0 MS (SIR) HMF 0.0 0.0 0.0.0.80.90.00.9 PDA.898.9 0 0.08 0.0 0.0 0.0.00.00.00.00.00.00 PDA (80 nm) HMF -.8 Chlorogenic Acid -.9 Catechin -.898 Caffeic Acid -.9 Epicatechin -..0.80.90.00.00.00.00.00.00.00 Figure. In this example, the ACQUITY SQ Detector provides greater specificity compared to the PDA. Catechin (Peak ), which was assigned and identified using UV retention times, was not detected and quantified by MS (as indicated by the red trace). Identification by UV alone might lead to an incorrect assignment of the polyphenol present, thereby causing mistaken identity of the fruit. The ACQUITY SQ Detector, with its greater specificity, can provide more confidence in data interpretation over a PDA detector alone. The ACQUITY SQ Detector can be easily added to routine QC laboratories that already use the ACQUITY UPLC H-Class System with Empower Software. Empower users can thereby reap the benefits of MS without the need for additional training. IntelliStart (an MS software component in Empower) enables easy setup and system monitoring of the SQ Detector. It also can automate the method development of selected ion recording (SIR) channels for new compounds.

Another advantage of the MS system is the ability to monitor SIR channels for each of the compounds in the target analysis list. Using the ACQUITY SQ Detector in this mode of operation allows the detector to be selective, and for the user, it is very easy to see whether a specific peak is present or absent in each sample analyzed. Furthermore, an additional benefit that results from the ACQUITY SQ Detector s selectivity is that the runtime can be reduced, since it is less important to obtain chromatographic resolution (compared to the UV detector) for each of the targeted and matrix peaks. For quantification of key components only, the analysis time was shortened from 0 min to min, (Method ), which improved sample throughput, as shown in Figure. 8x0 x0 Berry juices ( min) x0 x0 0.00.00.00.00.00.00.00 8.00 9.00.x0.0x0 8.0x0.0x0.0x0.0x0 0.0.x0.x0.0x0 8.0x0.0x0.0x0.0x0 0.0 8 9 0 Standard ( min) Figure. By utilizing the selectivity of the MS detector, the analysis run time can be shortened to increase sample throughput:.) arbutin,.) gallic acid, 8 Standard.) HMF, 9 (0 min).) chlorogenic acid,.) catechin,.) caffeic acid, 0.) epicatechin, 8.) p-coumaric acid, 9.) ferulic acid, 0.) phloridzin, and.) t-cinnamic acid..00.00.00.00.00.00.00 8.00 9.00.00.00.00.00.00.00.00 8.00 9.00 The polyphenol compounds identified and quantified by MS in the juice samples analyzed are listed in Table. Compound Apple Orange (Brand ) Orange (Brand ) Arbutin. Berries Guava Mango Lime Gallic acid 0. 0. 0..9 -hydroxymethyl-- furaldehyde (HMF). 0.8.0.9.9 Chlorogenic acid.... Catechin. Caffeic acid.9 0. Epicatechin 0. 0.0 0. 8. p-coumaric acid 0.9 Ferulic acid Phloridzin t-cinnamic acid Table. List of compounds in the fruit juice samples identified and quantified by MS. Values stated as ppm or mg/l. 8

C O N C LUSIONS In this work, the ACQUITY UPLC H-Class System, coupled with ACQUITY UPLC PDA and ACQUITY SQ detectors, enabled the separation, detection, identification, and quantification of polyphenols in fruit juices. The use of the ACQUITY UPLC H-Class System with Empower Software provides the familiarity of HPLC operation along with improved chromatographic performance and throughput of UPLC. References. Manach C, Scalbert A, Morand C, Rémésy C, Jiménez L. Am J Clinical Nutrition. 9():-, 00.. Seeram NP, Aviram M, Zhang Y, Henning SM et al. Comparison of Antioxidant Potency of Commonly Consumed Polyphenol-Rich Beverages in the United States. J Agric Food Chem. : -, 008.. Nagy K, Redeuil R, Bertholet R, Steiling H, Kussmann M. Anal Chem. 8: -, 009.. Wang X, Carr P W, Stoll, D R. LCGC North America. Vol 8 (): Nov 00. ACQUITY UPLC PDA with Empower Software increased the confidence in component identification beyond simple retention time matching with the UV spectra library functions. The ACQUITY SQ Detector with IntelliStart, provides the user with easy access to mass spectral information. This detector supports analytical labs performing quantification, data interpretation, and compound confirmation.. Rodriguez R, Picinelli Lobo A, Suarez Valles B. J Agric Food Chem. : 0-, 00.. Cooper K A, Campos-Giménez E, Jiménez Alvarez D, Nagy K, Donovan J L, Williamson G. J Agric Food Chem. : 8-8, 00.. Gledhill, A. Increasing Throughput by Run Time Reduction Leads to Greater Efficiency in Juice Laboratory. Waters application note no. 00090en, 008. Overall, the use of both PDA and MS detectors brings complementary benefits for QC laboratories doing routine QC analyses. Waters, ACQUITY, UPLC, and ACQUITY UPLC are registered trademarks of Waters Corporation. Empower, IntelliStart, and The Science of What s Possible are trademarks of Waters Corporation. All other trademarks are the property of their respective owners. 0 Waters Corporation. Produced in the U.S.A. August 0 00009en AG-PDF Waters Corporation Maple Street Milford, MA 0 U.S.A. T: 08 8 000 F: 08 8 990 www.waters.com