Iodide in Milk. Electrochemistry Discover the difference

Similar documents
Bisphenol A in Drinking Water

Mono- and Disaccharides

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

Carbohydrates in Food

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

Serotonin in Urine. Electrochemistry Discover the difference

HVA, VMA and 5-HIAA in Urine

Aminothiols and Disulfides

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

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

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

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

Analysis of Lactose and isomers in Lactose-free labelled products

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

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

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

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

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

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

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

[ APPLICATION NOTE ] Profiling Mono and Disaccharides in Milk and Infant Formula Using the ACQUITY Arc System and ACQUITY QDa Detector

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

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

Articaine & Epinephrine Injection According to USP Method

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

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

Oxidative Metabolism of Amodiaquine using the ROXY EC System

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

APPLICATION NOTE Determination of Aflatoxin M1 via FREESTYLE ThermELUTE with Online HPLC-Measurement

Ultrafast analysis of synthetic antioxidants in vegetable oils using the Agilent 1290 Infinity LC system

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

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

Authors. Abstract. Introduction. Environmental

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

Analysis of Acrylamide in French Fries using Agilent Bond Elut QuEChERS AOAC kit and LC/MS/MS

Rapid and Accurate LC-MS/MS Analysis of Nicotine and Related Compounds in Urine Using Raptor Biphenyl LC Columns and MS-Friendly Mobile Phases

Rapid Analysis of Water-Soluble Vitamins in Infant Formula by Standard-Addition

Determination of Amantadine Residues in Chicken by LCMS-8040

A Validated Chiral Liquid Chromatographic Method for The Enantiomeric Separation of Dapoxetine Hydrochloride

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

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

4.5 Minute Analysis of Benzodiazepines in Urine and Whole Blood Using LC/MS/MS and an Ultra Biphenyl Column

Extraction of Multiple Mycotoxins From Nuts Using ISOLUTE Myco prior to LC-MS/MS Analysis

Analysis of HMF by HPLC

A Novel Solution for Vitamin K₁ and K₂ Analysis in Human Plasma by LC-MS/MS

Determination of Carbohydrates in Kombucha Using HPAE-PAD

Extraction of Aflatoxin M1 From Infant Formula Using ISOLUTE Myco SPE Columns prior to LC-MS/MS Analysis

Application Note. Author. Abstract. Introduction. Food Safety

Journal of Chemical and Pharmaceutical Research

F. Al-Rimawi* Faculty of Science and Technology, Al-Quds University, P.O. Box 20002, East Jerusalem. Abstract

RP-HPLC Analysis of Temozolomide in Pharmaceutical Dosage Forms

Betadex Sulfobutyl Ether Sodium According to USP

Development and validation of stability indicating RP-LC method for estimation of calcium dobesilate in pharmaceutical formulations

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

Pelagia Research Library

AMIODARONE and DESETHYLAMIODARONE IN PLASMA BY UV FAST CODE Z33610

Rapid Gradient and Elevated Temperature UHPLC of Flavonoids in Citrus Fruit

HPLC Analysis of Sugars

Analysis of short chain organic acids in tobacco and in some flavored e-liquids

Determination of 6-Chloropicolinic Acid (6-CPA) in Crops by Liquid Chromatography with Tandem Mass Spectrometry Detection. EPL-BAS Method No.

Impurity Profiling of Carbamazepine by HPLC/UV

Application Note. Authors. Abstract. Food

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

Analysis of Cholesterol-Lowering Drugs (Statins) Using Dried Matrix Spot Technology

Carl Fisher, Terri Christison, Hua Yang, Monika Verma, and Linda Lopez Thermo Fisher Scientific, Sunnyvale, CA, USA

Extraction of Multiple Mycotoxins From Grain Using ISOLUTE Myco prior to LC-MS/MS Analysis

DEVELOPMENT OF RP-HPLC METHOD FOR ESTIMATION OF DROTAVERINE HYDROCHLORIDE IN PHARMACEUTICAL FORMULATIONS

Maximizing chromatographic peak capacity with the Agilent 1290 Infinity LC system

Analysis of bisphenol A leaching from baby feeding bottles

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

A Simple and Accurate Method for the Rapid Quantitation of Drugs of Abuse in Urine Using Liquid Chromatography

Determination of Sucralose Using HPAE-PAD

Unequalled durability against water elution. % tr

Optimization of extraction method and profiling of plant phenolic compounds through RP-HPLC

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

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

Journal of Chemical and Pharmaceutical Research, 2013, 5(1): Research Article

Scholars Research Library

METHOD DEVELOPMENT AND VALIDATION BY RP-HPLC FOR ESTIMATION OF ZOLPIDEM TARTARATE

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

Analytical Method Development and Validation for the Estimation of Guaifenesin and Dextromethorphan by RP-HPLC

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

Quantitative Analysis of Drugs of Abuse in Urine using UHPLC Coupled to Accurate Mass AxION 2 TOF Mass Spectrometer

Betadex Sulfobutyl Ether Sodium according to USP

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

AMIODARONE and DESETHYLAMIODARONE IN PLASMA BY UV FAST CODE Z33610

Comprehensive Two-Dimensional HPLC and Informative Data Processing for Pharmaceuticals and Lipids

Development and Validation of Multiresidue Pesticide Methods at FDA/CFSAN

The LC Column Playbook

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

Institute of Toxicology Clinical Toxicology and Pharmacology Berliner Betrieb für Zentrale Gesundheitliche Aufgaben, Berlin

ISSN: ; CODEN ECJHAO E-Journal of Chemistry 2011, 8(3),

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

Tentu Nageswara Rao et al. / Int. Res J Pharm. App Sci., 2012; 2(4): 35-40

IJPAR Vol.3 Issue 4 Oct-Dec-2014 Journal Home page:

Determination of Plant-Derived Neutral Oligo- and Polysaccharides Using the CarboPac PA200

Determination of Pharmaceutical Residues in Bovine Milk via LC MS/MS Following Solid Phase Extraction

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

A HPAE-PAD Chromatographic Assay for Carbohydrates in Urine as a Measure of Intestinal Permeability

Transcription:

Application Note Food & Beverage The finest LC-EC Applications for Food & Beverage analysis Iodide 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 FlexCell with exchangeable working electrode n Diamond working electrode n Robust and reproducible analysis Summary In this application note a sensitive and reliable LC-EC method is presented for the analysis of iodide based on DC amperometry using a flow cell with a diamond working electrode. Conductive diamond has several advantages over conventional electrode materials such as a wide potential window in aqueous solutions, excellent chemical inertness and stability. ALEXYS Application Note # 212_004_03 Electrochemistry Discover the difference

Introduction Iodine is an essential trace element for humans. It is a component of the thyroid hormone thyroxin, which regulates the body s metabolic state and the growth and development in children. Iodine deficiency is an important health problem throughout much of the world. The dietary uptake of sufficient trace amounts of iodide is therefore necessary for mental and physical development. Important sources of iodide are seafood, diary products, iodized table salt and processed foods like iodized bread [1]. Table 1 LC-EC Conditions HPLC ALEXYS Iodide Analyzer (part no 180.0095E) Flow rate 0.4 ml/min Flow cell FlexCell with MD WE and HyREF Temperature 35 C for separation and detection Range 2 μa/v ADF 0.5 Hz I-cell 10-30 na HPLC in combination with electrochemical detection is commonly used for the analysis of iodide in urine [2,3] and food products [4,5]. 2 na Iodide Figure 1: ALEXYS Iodide Analyzer. 0 5 10 15 Time [min.] Figure 2: Chromatogram of a 400 nm of potassium iodide (KI) in water (50.8 μg/l Iodide).Injection volume 20 μl. Method The ALEXYS Iodide analyzer is equipped with a DECADE Elite electrochemical detector and FlexCell with replaceable diamond electrode disc. The LC conditions used with the ALEXYS Iodide Analyzer were selected with the focus on the analysis of iodide in dairy products. Therefore, the same mobile phase and similar separation conditions were used as described in literature [4,5]. 2

Results A hydrodynamic voltammogram was recorded in the potential range between 900 and 2400 mv (vs. HyREF) to determine the optimum detection potential, using a 10 μm KI solution in water. Although the onset of the limiting current was observed at 2000 mv, a lower potential of 1500 mv was chosen for detection. At this potential a low background current (<30 na) and noise level are attained in combination with a good detection sensitivity for Iodide. In Figure 2 an example chromatogram is shown of 50.8 μg/l potassium iodide in water (injection volume 20 μl). The peak efficiency for the iodide peak was 69.000 theoretical plates/meter. Linearity and detection limits Calibration curves were recorded with Iodide standards in the concentration range between 6 μg/l 1.3 mg/l. Within this concentration range a linear detector response was observed with correlation coefficients better than 0.999. Iodide Area ( μa.s) 5 4 3 2 1 0 0.0 0.3 0.5 0.8 1.0 1.3 1.5 Iodide concentration (mg/l) 5 na Figure 4: Calibration plot for Iodide in water. Concentration range 6 μg/l 1.3 mg/l. R = 0.9999. Iodide 0 5 10 15 Time [min.] Figure 3: Chromatogram of Iodide in low-fat (1.5%) milk sample. Injection volume 20 μl. 3

A concentration detection limit (clod) of approximately 0.4 μg/l (3 nm) was found, demonstrating the excellent detection sensitivity achieved with the MD electrode. The clod is based on an injection volume of 20 μl and defined as the concentration that gives a signal that is three times the peakto-peak noise. Repeatability The repeatability of the method was evaluated by executing 10 repetitive injections (20 μl injection volume) of a 0.13 mg/l and 1.23 mg/l iodide solution. The relative standard deviation (RSD%) for retention time, peak area and height are listed in Table 2 for both concentrations. The relative standard deviation for both peak height and peak area are 1% or better at a concentration of 0.13 mg/l and 0.2-0.3% at 1.26 mg/l. The long-term repeatability was assessed with a standard with a high iodide concentration of 13.7 mg/l. 225 repetitive injections were performed in a time period of 22 hours, see Figure 5. For this experiment the flow rate was increased with a factor 2 (0.8 ml/min, system backpressure approximately 180 bar) to reduce the analysis time (6 minutes). After the 20 th injection a gap of 6 injections is visible due to an empty vial. 50 Table 2 Repeatability (n=10) Iodide (mg/l) tr Area Height 0.13 0.1 0.9 1.0 1.26 0.1 0.2 0.3 Iodide Area ( A.s) 40 30 20 10 0 0 50 100 150 200 250 Number of injections Figure 5: Long-term repeatability of DC amperometric detection of iodide on an MD electrode. Sample concentration 13.7 mg/l, injection volume 20 μl. The relative standard deviations (RSD%) for the peak area was 1.4%. It demonstrates the good response stability of MD, even at high iodide concentration. It has been observed that online electrochemical regeneration/ activation is an effective method to restore the detection sensitivity in case the response of the Magic Diamond electrode attenuated over time, or the electrode has not been used for a while. The flow cell does not have to be disassembled in this case. During the online regeneration procedure the detector was operated in the SCAN mode. Typically, the electrode was scanned between 3 Volts and + 3 Volts in mobile phase, with a scan rate of 50 mv/s.. 4

Iodide in milk products In Figure 3 an example chromatogram of a low-fat (1.5%) milk sample is shown. The following sample preparation procedure was performed prior to injection n 1 ml 3% acetic acid was mixed with 5 ml of sample for deproteination of the milk solution. The acidified solution was centrifuged and the supernatant collected. n Subsequently, the supernatant was passed over a RP SPE column (Alltech C18-fast column) for further clean-up of the milk matrix (removal of fat). n The eluate (first 2 ml discarded) was collected and 20 ul injected in the LC system. It should be stated that the sample preparation procedure described above is not validated and is only used to obtain a series of example chromatograms. The iodide peak in the chromatogram was identified by spiking a second milk sample prior to sample work-up with a known amount of Iodide, corresponding to a concentration of 317 μg/l. It is evident from Figure 3 that the iodide peak is well separated from the matrix. The concentration of iodide in the milk sample was estimated to be 45 μg/l. Conclusion The ALEXYS Iodide Analyzer provides a user-friendly and reliable solution for the determination of iodide by means of DC amperometry. With the new inert Magic Diamond electrode, iodide can be detected with excellent reproducibility and sensitivity. 5

References 1. John T. Dunn, Editorial: What s happening to our Iodine?, J Clin Endocrinol Metab., 83(10), 1998, 3398-400 2. K.Han, W. Koch, K.W. Pratt, Improved procedure for the determination of Iodide by Ion Chromatography with Electrochemical detection, Anal. Chem., 59, 1987, 731-736 3. J. Rendl, S. Seybold, W. Borner, Urinary Iodide determined by Paired-Ion Reversed Phase HPLC with Electrochemical de-tection, Clin. Chem., 40/6, 1994, 908-913 4. Determination of iodide content in milk and dried milk by HPLC, International IDF standard, 167:1994 5. Milk and dried milk Determination of iodide contents method using HPLC, International ISO standard, 14378:2000 6. W.R. LaCourse, Pulsed Electrochemical Detection in High Performance Liquid Chromatography, John Wiley & Sons, New York, 1 ed,1997. 7. Alexander Kraft, Doped diamond: A compact review on a new, versatile electrode material, Int. J. Electrochem. Sci., 2, 2007, 355-385 Ordering information 180.0095E ALEXYS Iodide Analyzer 250.1104 ALE-315 column, 150x3.0mm, 3um C18 Antec Scientific (USA) info@antecscientific.com www.antecscientific.com T 888 572 0012 Antec Scientific (worldwide) info@antecscientific.com www.antecscientific.com T +31 71 5813333 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. 6