Bisphenol A in Drinking Water

Similar documents
Iodide in Milk. Electrochemistry Discover the difference

Mono- and Disaccharides

Application Note. Authors: C. Ledesma, M. Gibert, J.R. Gibert Ingenieria Analitica S.L. Extracts from various food products

Determination of Bisphenol A in Milk Powder using a Chromolith HighResolution RP-18 endcapped column

Analysis of bisphenol A leaching from baby feeding bottles

Application Note. Agilent Application Solution Analysis of ascorbic acid, citric acid and benzoic acid in orange juice. Author. Abstract.

Carbohydrates in Food

Qualitative and quantitative determination of phenolic antioxidant compounds in red wine and fruit juice with the Agilent 1290 Infinity 2D-LC Solution

Serotonin in Plasma. Electrochemistry Discover the difference. Summary. Application Note Clinical & Diagnostics

Application Note. Agilent Application Solution Analysis of fat-soluble vitamins from food matrix for nutrition labeling. Abstract.

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

Serotonin in Urine. Electrochemistry Discover the difference

Metanephrines. in Urine. Clinical & Diagnostics Analysis. Introduction. Application Note ALEXYS - Clinical & Diagnostics

Analytical Method Development for USP Related Compounds in Paclitaxel Using an Agilent Poroshell 120 PFP

Rapid Gradient and Elevated Temperature UHPLC of Flavonoids in Citrus Fruit

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

Rapid and sensitive UHPLC screening of additives in carbonated beverages with a robust organic acid column

Application Note. Small Molecule Pharmaceuticals. 2-Ethyl-2-phenylmalonamide Ethosuximide Primidone Carbamazepine. Carbamazepine-

Chiral Multicolumn Method Development on the Agilent 1260 Infinity II SFC System

Agilent 1220 Infinity LC System Performance Specifications

Rapid and sensitive UHPLC screening for water soluble vitamins in sports beverages

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

HVA, VMA and 5-HIAA in Urine

Iodine HPLC Assay. Catalog Number: IOD34-H Tests For Research Use Only. Not for use in diagnostic procedures.

Separation of Polyphenols by Comprehensive 2D-LC and Molecular Formula Determination by Coupling to Accurate Mass Measurement

Determination of Clinically Relevant Compounds using HPLC and Electrochemical Detection with a Boron-Doped Diamond Electrode

BPA-based materials, such as polycarbonate and epoxy resins, have a huge socioeconomic

Transferring a Method for Analysis of DNPH-Derivatized Aldehydes and Ketones from HPLC to UHPLC

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

Shuguang Li, Jason Anspach, Sky Countryman, and Erica Pike Phenomenex, Inc., 411 Madrid Ave., Torrance, CA USA PO _W

USP purity analysis of pravastatin sodium using the Agilent 1120 Compact LC

The Determination of Sugars in Molasses by High-Performance Anion Exchange with Pulsed Amperometric Detection

Maximizing Efficiency Using Agilent InfinityLab Poroshell 120 Columns

Product Guide for LudgerSep TM R1 HPLC Column for DMB labelled Sialic Acid Analysis

25-Hydroxyvitamin D2-D3 Serum VD-200 UHPLC Analysis Kit User Manual

Application Note. Abstract. Author. Biotherapeutics & Biosimilars. Sonja Schneider Agilent Technologies, Inc. Waldbronn, Germany

Rapid and Direct Analysis of Free Phytosterols by Reversed Phase HPLC with Electrochemical Detection

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

Selectivity Comparison of Agilent Poroshell 120 Phases in the Separation of Butter Antioxidants

Oxidative Metabolism of Amodiaquine using the ROXY EC System

Agilent 1260 Infinity Analytical SFC System

Robust extraction, separation, and quantitation of structural isomer steroids from human plasma by SPE-UHPLC-MS/MS

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

Product Guide for LudgerSep TM ur2 UHPLC Column for DMB Sialic Acid Analysis

Performance Characteristics of the Agilent 1290 Infinity II Multicolumn Thermostat

Impurity Profiling of Carbamazepine by HPLC/UV

Sample Concentration and Analysis of Human Hormones in Drinking Water

ANTEC LEYDEN. Analysis of Carbohydrates in Food and Beverages using Anion-Exchange Chromatography and Pulsed Amperometric. Introduction.

Determination of Tetracyclines in Chicken by Solid-Phase Extraction and High-Performance Liquid Chromatography

EASI-EXTRACT BIOTIN Product Code: P82 / P82B

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

Optimizing Chiral Separations and Purification of Enantiomers Through Selective Sample Slicing and Column Switching

Analysis of Lactose and isomers in Lactose-free labelled products

Unequalled durability against water elution. % tr

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

Analysis of Common Sweeteners and Additives in Beverages with the PerkinElmer Flexar FX-15 System Equipped with a PDA Detector

Application Note. Author. Abstract. Introduction. Food Safety

Mass-Based Purification of Natural Product Impurities Using an Agilent 1260 Infinity II Preparative LC/MSD System

LC-MS/MS analysis of Chlorates in Milk and Whey Powder using the Agilent 6470 QQQ

RP-HPLC Analysis of Temozolomide in Pharmaceutical Dosage Forms

Cannabinoid Profiling and Quantitation in Hemp Extracts using the Agilent 1290 Infinity II/6230B LC/TOF system

Determination of Benzoate in Liquid Food Products by Reagent-Free Ion Chromatography

Lipidomic Analysis by UPLC-QTOF MS

Analysis of Chloride, Phosphate, Malate, Sulfite, Tartrate, Sulfate, and Oxalate in Red and White Wine

ALEXYS Neurotransmitter Analyzer

Sugar analysis according to the EU Regulation using amperometric detection and Metrosep Carb 2-150/4.0

Fig.1. Denatonium benzoate (DB) chemical structure

SPE-LC-MS/MS Method for the Determination of Nicotine, Cotinine, and Trans-3-hydroxycotinine in Urine

Analysis of Isoflavones with the PerkinElmer Flexar FX-15 UHPLC System Equipped with a PDA Detector

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

Aminothiols and Disulfides

Asian Journal of Pharmaceutical Analysis and Medicinal Chemistry Journal home page:

Vitamin D Metabolite Analysis in Biological Samples Using Agilent Captiva EMR Lipid

Determination of enantiomeric purity of Timolol Maleate by Supercritical Fluid Chromatography

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

Development and Validation of a Polysorbate 20 Assay in a Therapeutic Antibody Formulation by RP-HPLC and Charged Aerosol Detector (CAD)

Analysis of Vitamins Using an SFC/UHPLC Hybrid System with a Triple Quadrupole LC/MS for Quantification

EASI-EXTRACT FOLIC ACID Product Code: P81 / P81B

Chiral Screening for SFC and UHPLC with the Agilent 1260 Infinity II SFC/UHPLC Hybrid System

Ultra High Performance Liquid Chromatograph. Nexera X2 C196-E079

Alexys Neurotransmitter Analyzer for Monoamines and Metabolites

LC-MS/MS Method for the Determination of Tenofovir from Plasma

Converting a CHP Method for Insulin to Agilent Poroshell 120 Columns

Carnitine / Acylcarnitines Dried Blood Spots LC-MS/MS Analysis Kit User Manual

Authors. Abstract. Introduction. Environmental

VITAMINES A / E IN PLASMA BY UV - FAST CODE Z18610

Simultaneous Analysis of Norepinephrine, Dopamine and Serotonin in 15 Minutes

Simultaneous Estimation of Gemcitabine Hydrochloride and Capecitabine Hydrochloride in Combined Tablet Dosage Form by RP-HPLC Method

Simultaneous Quantitative Analysis of Total Catecholamines and Metanephrines in Urine Using CLEAN UP CCX2 and LC-MS/MS

Application Note. Sensitive analysis of the lactose content of lactose-free labelled products using HPAEC-PAD. Summary.

Analysis of Counterfeit Antidiabetic Drugs by UHPLC with the Agilent 1220 Infinity Mobile LC

Analysis of Amino Acids Derived Online Using an Agilent AdvanceBio AAA Column

CORESTA Recommended Method No. 78

Quantification of lovastatin in human plasma by LC/ESI/MS/MS using the Agilent 6410 Triple Quadrupole LC/MS system

HPLC Analysis of Sugars

Determination of taurine in energy drinks by high-performance liquid chromatography

Transcription:

Application Note Food & Beverage The finest LC-EC Applications for Food & Beverage analysis Bisphenol A Phenols Bisphenol A Catechins Flavonoids Phenols Antioxidants Resveratrol Epicatechin Quercetin Other polyphenols Carbohydrates Monosaccharides Lactose Other oligo- and polysaccharides Vitamins, minerals etc. A, C, D, E, and K Iodide Q10, ubiquinols n Binary gradient HPLC n Analysis of food and beverages n Robust & reproducible analysis Summary Concerns have been expressed about the estrogenicity of BPA and other aromatic components that leached from commercial products into food and beverages. In this note a sensitive method is presented to analyse drinking water from bottles and cans on the presence of BPA. An ALEXYS system is used in combination with a solid phase sample pre-concentration step. A detection limit of 0.5 nmole/l has been obtained. ALEXYS Application Note # 216_005_06 Electrochemistry Discover the difference

Introduction Bisphenol A (BPA) is an important chemical building block that is used primarily to make polycarbonate plastic and epoxy resins, both of which are used in a wide variety of applications. Common examples of polycarbonate products include eyeglass lenses, digital media (e.g., CDs, DVDs), electronic and electrical equipment housings (e.g., personal computers, appliances, power tools), automobile headlight lenses, sports safety equipment (e.g., helmets, goggles), and reusable food and drink containers. When used as a coating on the interior of metal cans, epoxy resins protect the integrity and quality of our food supply by preventing corrosion and contamination of canned foods and beverages with metals. An ALEXYS system is used in combination with a solid phase sample pre-concentration step. A 1 ml sample volume is loaded onto a pre-column by a user program in the AS 100 autosampler. For this purpose the AS 100 has been equipped with a 10-port valve. A second pump is used to supply the washing solvent. Advantages of using the pre-column is not only an improvement of detection limit, but also the chromatography and sample clean-up. Experiments with 1000 μl injections without pre-column showed a large front peak and a considerable shift in retention times. By applying a precolumn this front peak and also the drift in the baseline are significantly reduced. Results Hydrodynamic voltammogram To find the optimum detection potential BPA was analysed at potential settings between 500 and 1200 mv (vs HyREF) using 10 μl injections of a 500 nmol/l BPA standard. The optimum potential that gives the best s/n ratio is 900 mv. 10 Figure 1: ALEXYS Bisphenol A Analyzer. Method peak height (na) 8 6 4 2 Table 1 LC-EC Conditions HPLC Temperature ALEXYS Bisphenol A Analyzer 35 C (separation and detection) Column Analytical: ALF 215 150 X 2.1 mm, 3μm ALH pre-column 5 x 1 mm, 5μm Flow cell VT-03 with 2 mm GC WE, HyREF Flow rate A: 200 μl/min B: 800 μl/min (pump 2, pre-concentration) Pressure A: 9 MPa Ecell 900 mv 0 400 600 800 1000 1200 E (mv) Figure 2: Hydrodynamic voltammogram for BPA. 2

Electrode contamination Analysis of relatively high concentrations of BPA showed a decrease in peak height of about 50% after 100 injections. After polishing the working electrode the signal was restored to the original peak height. This shows that at elevated concentrations of BPA electrode contamination is an issue. At lower concentration levels no contamination has been observed. A 10 8 peak height (na) 6 4 2 B 0 0 20 40 60 80 injections Figure 4: Decrease in peak heights of 500 nm BPA (10 μl) on a 3 mm column due to electrode contamination. 0.6 0.5 C Figure 3: User program for BPA analysis. A 1 ml loop is filled with sample [A]. The 10-port valve switches and pump 2 with solvent B carries the sample onto the pre-column [B]. The valve switches back and the pump 1 with solvent A flushes the concentrated sample from the pre-column onto the analytical column. Meanwhile, filling of the 1 ml sample loop is started. peak height (na) 0.4 0.3 0.2 0.1 0 0 50 100 150 200 injections For the construction of a hydrodynamic voltammogram a 3mm ID column and a flow cell with 3 mm working electrode has been used. Figure 5: Peak heights of 5 nm BPA (10 μl) on a 2 mm column, 200 replicate injections. No electrode contamination has been observed In cases where electrode contamination is an issue a cleaning pulse can be applied. Typically, the potential is set to a reductive potential for about one minute. After about one minute the detection potential is applied and after a few minutes stabilisation period the system is ready for analysis. We found that switching the potential to +100 mv for 54 s is sufficient to prevent electrode contamination. 3

Linearity The linearity has been studied in the range 0.1-10 nm BPA. Below 0.5 nm the results were not linear and these data points are rejected (Fig. 6). Correlation coefficient r is better than 0.999. From this calibration data a detection limit of 0.3 nm was found. Calculation using the signal-to-noise ratio [LOD = 3 n c / s] results in a factor 10 better detection limit. However, practical detection limit is higher because of non-linearity at lower concentrations. na 12.5 12.0 11.5 25.0 20.0 3 4 5 6 min signal 15.0 10.0 5.0 0.0 0.00 2.00 4.00 6.00 8.00 10.00 concentration Figure 6: Calibration curve of BPA: Y = 0.0843 + 2.2072 X. Signal is peak height in na, concentration in nmol/l. Figure 8: Overlay of chromatograms of 2.5 nm BPA (n=9) Reproducibility Reproducibility is studied for standard injections of 0.5 nm, 1 nm and 2.5 nm BPA (1000 μl). In Fig. 7 - Fig. 8 overlays of chromatograms of 0.5 nm and 2.5 nm BPA are shown. The results are summarized in Table 2. For areas and peak heights the %RSD is the same, about 2%. na 14.2 14.0 13.8 Table 1 Repeatability C (nm) t (min) %RSD h (na) %RSD n 0.5 5.52 0.1 0.33 1.9 5 1.0 5.52 0.1 0.64 1.2 8 2.5 5.51 0.1 1.45 1.8 9 13.6 13.4 13.2 4 5 6 7 8 9 min Figure 7: Overlay chromatograms of reproducibility study of 0.5 nm BPA (5.5 min, n=5) 4

Analysis of drinking water Drinking water from 2 different PET bottles (Spa, Sourcy) and from a polycarbonate container of an aqua machine (Nestlé) was analysed. The PET bottles were free of BPA. In water from the aqua machine a concentration level of 1.5 nm BPA was found. References 1. Environmental Health Perspectives 108 (1) (2000) 21. Determination of Bisphenol A and Related Aromatic Compounds Released from Bis-GMA-Based Composites and Sealants by High Performance Liquid Chromatography 2. Journal of Chromatography B, 736 (1999) 255-261. Sensitive method for the determination of bisphenol-a in serum using two systems of high-performance liquid chromatography na 16 water_1 water_3 water_4 15 1 nm 0.5 nm BPA 14 13 0 1 2 3 4 5 6 7 8 9 min Figure 9: Overlay of chromatograms of water samples (3 upper traces) and standards (2 lower traces: 0.5 and 1 nmol/l). Only water sample no 1 contained BPA (1.5 nmol/l). Conclusion An ALEXYS system has been used for the analysis of BPA in drinking water. A 10-port valve was used in combination with a pre-column for sample pre-concentration and clean-up. A detection limit of 0.3 nm has been obtained. At 0.5 nm an RSD of better than 2% for peak heights and areas was found. 5

Ordering information 180.0090B ALEXYS Bisphenol A Analyzer 250.1120 ALF-215 column, 150x2.1mm, 3um C18 250.1132 ALH pre-column cartridge 5 x 1 mm ID, 5 μm, 5pk 250.1134 ALH pre-column holder, 5mm Antec Scientific (USA) info@antecscientific.com www.antecscientific.com T 888 572 0012 For research purpose only. The information shown in this communication is solely to demonstrate the applicability of the ALEXYS system. The actual performance may be affected by factors beyond Antec s control. Specifications mentioned in this application note are subject to change without further notice. Antec Scientific (worldwide) info@antecscientific.com www.antecscientific.com T +31 71 5813333 6