Mercury Speciation Determinations in Asian Dietary Supplements

Similar documents
Detection and Quantification of Inorganic Arsenic in Fruit Juices by Capillary Ion Chromatography with Suppressed Conductivity Detection

Determination of Inorganic Ions and Organic Acids in Non-Alcoholic Carbonated Beverages

Rapid determination of phosphate and citrate in carbonated soft drinks using ion chromatography

Determination of Ethyl Sulfate Impurity in Indinavir Sulfate Drug Using Ion Chromatography

Improved Extraction and Analysis of Hexavalent Chromium from Soil and Water

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

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

Identification and Quantification at ppb Levels of Common Cations and Amines by IC-MS

Measuring Phytosterols in Health Supplements by LC/MS. Marcus Miller and William Schnute Thermo Fisher Scientific, San Jose, CA, USA

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

IC-MS Environmental Applications - Water Testing. Application Notebook

Determination of Carbohydrates in Kombucha Using HPAE-PAD

Determination of Carbohydrates in Beverages and Milk Products by HPAE-PAD and Capillary HPAE-PAD

Separation of Chromium (III) and Chromium (VI) by Ion Chromatography

High-Throughput, Cost-Efficient LC-MS/MS Forensic Method for Measuring Buprenorphine and Norbuprenorphine in Urine

Sialic Acid Determination in Glycoproteins: Comparison of Two Liquid Chromatography Methods. Experimental. Introduction. Method 1.

Determination of Trace Sodium in Cranberry Powder

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

Determination of Organic Acids in Kombucha Using a High-Pressure Ion Chromatography System

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

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

Rapid Determination of Phosphate and Citrate in Carbonated Soft Drinks Using a Reagent-Free Ion Chromatography System

The Investigation of Factors Contributing to Immunosuppressant Drugs Response Variability in LC-MS/MS Analysis

Determination of Carbachol In Ophthalmic Solutions Using a Reagent-Free Ion Chromatography System

MS/MS as an LC Detector for the Screening of Drugs and Their Metabolites in Race Horse Urine

Application Note 178 INTRODUCTION

Comparison of Full Scan MS2 and MS3 Linear Ion Trap Approaches for Quantitation of Vitamin D

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

Determination of Water- and Fat-Soluble Vitamins in Nutritional Supplements by HPLC with UV Detection

Application Note 178. Brian DeBorba and Jeff Rohrer Thermo Fisher Scientific, Sunnyvale, CA, USA. 10 Typically, this requires the use of sample

Impurity Profiling of Carbamazepine by HPLC/UV

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

A New HILIC/RP Mixed-Mode Column and Its Applications in Surfactant Analysis

GC-MS/MS Analysis of Benzodiazepines Using Analyte Protectants

Robust and Fast Analysis of Tobacco-Specific Nitrosamines by LC-MS/MS

LC-MS/MS Method for the Determination of 21 Opiates and Opiate Derivatives in Urine

Fast UHPLC Methods for Analysis of Amino Acids

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

A Rapid UHPLC Method for the Analysis of Biogenic Amines and Metabolites in Microdialysis Samples

Increasing Extraction Efficiency of Wet Samples Using a Novel New Polymer During Accelerated Solvent Extraction

Evaluation of an LC-MS/MS Research Method for the Analysis of 33 Benzodiazepines and their Metabolites

High-Throughput Quantitative LC-MS/MS Analysis of 6 Opiates and 14 Benzodiazepines in Urine

Determination of Methacholine Chloride and Potential Impurities Using a Reagent-Free Ion Chromatography System

Ion Chromatography: A Versatile Technique for the Analysis of Beer

Doubling the throughput of long chromatographic methods by using a novel Dual LC workflow

Quantitative Analysis of THC and Main Metabolites in Whole Blood Using Tandem Mass Spectrometry and Automated Online Sample Preparation

Enhanced LC-MS Sensitivity of Vitamin D Assay by Selection of Appropriate Mobile Phase

Solving One of Chromatography s Biggest Dilemmas Proper Sealing of Chromatography Autosampler Vials

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

Dayana Argoti, Kerry Hassell, Sarah J. Fair, and Joseph Herman Thermo Fisher Scientific, Franklin, MA, USA

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

Thermo Fisher Scientific, Sunnyvale, CA, USA; 2 Thermo Fisher Scientific, San Jose, CA, USA

A New Era in SFC Column Technology

THE POWER OF MASS SPECTROMETRY FOR IC ANALYTICAL CHEMISTS. Unleash New Possibilities with Enhanced Detection for IC Applications

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

Separation of 2AA-Labeled N-Linked Glycans from Glycoproteins on a High Resolution Mixed-Mode Column

HPAE-PAD Determination of Infant Formula Sialic Acid

1 out of 8. Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 86th Meeting 2018 ERYTHROSINE

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

Integrated Targeted Quantitation Method for Insulin and its Therapeutic Analogs

Marc Plante, Bruce Bailey, and Ian N. Acworth Thermo Fisher Scientific, Chelmsford, MA, USA

Determination of Polymerized Triglycerides by High Pressure Liquid Chromatography and Corona Veo Charged Aerosol Detector

Rev. CO Packed Columns for Ion Chromatography

Characterization of Used Cooking Oils by High Performance Liquid Chromatography and Corona Charged Aerosol Detection

A Versatile Detector for the Sensitive and Selective Measurement of Numerous Fat-Soluble Vitamins and Antioxidants in Human Plasma and Plant Extracts

Analysis of Phospholipids in Natural Samples by Normal Phase HPLC and Corona Charged Aerosol Detection

Thermo Scientific Dionex CarboPac MA1 Column

Determination of Tigecycline in a Cell Lysate

Lutein Esters from Tagetes Erecta

Bioanalytical Quantitation of Biotherapeutics Using Intact Protein vs. Proteolytic Peptides by LC-HR/AM on a Q Exactive MS

Direct Determination of Native N-linked Glycans by UHPLC with Charged Aerosol Detection

ApplicationNOTE EXACT MASS MEASUREMENT OF ACTIVE COMPONENTS OF TRADITIONAL HERBAL MEDICINES BY ORTHOGONAL ACCELERATION TIME-OF-FLIGHT.

Detection of oxygenated polycyclic aromatic hydrocarbons (oxy-pahs) in APCI mode with a single quadrupole mass spectrometer

TENOFOVIR TABLETS: Final text for addition to The International Pharmacopoeia (June 2010)

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

FT-Raman Surface Mapping of Remineralized Artificial Dental Caries

Ensuring High Sensitivity and Consistent Response in UHPLC-MS Analyses

Nitrogen/Protein Determination in Starch by Flash Combustion using Large Sample Weight as an Alternative to the Kjeldahl Method

Use of a Tandem Mass Spectrometry Research Method for the Analysis of Amino Acids and Acylcarnitines in Dried Blood Spots

Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016.

Results of Using Re-washed Vials and Closures

GlycanPac AXR-1 Columns

Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016.

Determination of perchlorate in environmental waters using a compact ion chromatography system coupled with a single quadrupole mass spectrometer

Thermo Scientific. GlycanPac AXR-1. Column Product Manual. P/N: April, Part of Thermo Fisher Scientific

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

Analysis of HMF by HPLC

Improving Food Process Control Using the

Optimizing Sample. Chromium Analyses in Waters. Jane Timm, James Lovick Jr, Raymond Siery, ato 2011 NEMC, Bellevue, Washington

columns CarboPac PA20 Column

Analytical Method for 2, 4, 5-T (Targeted to Agricultural, Animal and Fishery Products)

Analysis of Emulsifiers in Foods by High Pressure Liquid Chromatography and Corona Charged Aerosol Detection

Development of Ion Chromatography Methods to Support Testing of the Glycolic Acid Reductant Flowsheet in the Defense Waste Processing Facility

ab Hemoglobin Assay Kit (Colorimetric)

INTRODUCTION. Application Note 176

Direct Analysis of Multicomponent Adjuvants by HPLC with Charged Aerosol Detection

SUPPLEMENTARY MATERIAL

Tenofovir disoproxil fumarate (Tenofoviri disoproxili fumaras)

Transcription:

Mercury Speciation Determinations in Asian Dietary Supplements Terri Christison, Deepali Mohindra, Frank Hoefler, and Linda Lopez, Thermo Fisher Scientific, Sunnyvale, California, USA

Overview Purpose: Demonstrate low cost solutions for use in food safety for mercury speciation and counter anion determinations in solutions extracted from dietary supplements on an integrated ion chromatography system. Methods: Mercury species (mg/l) were determined on a mixed anion-cation-exchange column optimized for metal speciation using a cysteine-perchlorate eluent and detected by absorbance at 210 nm. Inorganic anions and organic acids were determined on an anion-exchange high-capacity column optimized for organic acids using electrolytically generated hydroxide eluent and detected by suppressed conductivity detection. Results: The Asian supplements had 0.05 to 0.1 wt% extractable amounts primarily of less toxic inorganic mercury. Introduction Multiple patients had clinical symptoms of mercury poisoning and unusually high blood concentrations (mg/dl) of total mercury after ingesting Asian dietary supplements adulterated with mercury. Testing of the dietary supplements by Inductively Coupled Plasma (ICP) showed they contained 10,000-fold higher concentrations of total mercury (1 10 wt%) than measured in the patients blood. Because inorganic and organic forms of mercury show disparate toxicity, mercury speciation was required to establish the forms of mercury present in the supplement for determining food safety. Counter-anion determinations were also needed to calculate mass balance. Ion chromatography (IC) is well suited for ion separations and provides a well-established method to determine and quantify metal species and anions. Methods Sample Preparation The Asian dietary supplements were ground to a coarse powder, extracted in 20 ml of eluent with manual agitation for 5 min, filtered, diluted with deionized water prior to injection for mercury speciation determinations. The samples were treated in the same manner and extracted with deionized water for counter anion determinations. Standard Preparation The methylmercury and ethylmercury standards were prepared from their mercury salts (Aldrich) in methanol, and diluted with water to the working standard concentrations. All other standards were prepared in deionized water. Instrument Method 1: Mercury Speciation By Ion Pairing Chromatography Thermo Scientific Dionex ICS-1600 Standard Integrated or Dionex ICS-1100 Basic Integrated IC system Thermo Scientific Dionex ICS Series Variable Wavelength Detector (VWD) Thermo Scientific Dionex AS-AP Autosampler Method 2: Counter Anion Determinations By Ion Chromatography Dionex ICS-2100 Integrated Reagent-Free IC (RFIC ) system Dionex AS-AP Autosampler Software Thermo Scientific Dionex Chromeleon Chromatography Data System 2 Mercury Speciation Determinations in Asian Dietary Supplements

FIGURE 1. Dionex AS-AP Autosampler (Bottom Left), Dionex ICS Series VWD (Top Left) shown next to Dionex ICS-1600 (Center), and ICS-2100 RFIC (Right) Integrated IC Systems. Method 1: Ion Pair Chromatography Columns: Thermo Scientific Dionex IonPac CG5A, CS5A, 4 x 250 mm Eluent 1.0 mm acetic acid, 1.0 mm sodium perchlorate, 5 mm cysteine, adjusted to ph = 4.0 Flow Rate: 1.75 ml/min Injection Volume: 25 µl Detection: UV Absorbance, 210 nm Method 2: Counter Anion Determinations Using Reagent-Free Ion Chromatography Columns: Dionex IonPac AG11-HC, AS11-HC, 4 250 mm Eluent Source: Thermo Scientific Dionex EGC III KOH cartridge Gradient: 1.0 mm KOH for 8 min, 1 15 mm KOH from 8 to 18 min, 15 20 mm KOH from 18 to 28 min, 30 60 mm KOH from 28 to 38 min, 1 mm KOH from 38 to 45 min Flow Rate: 1.5 ml/min Injection Volume: 25 µl Detection: Suppressed conductivity, Thermo Scientific Dionex ASRS 300 Anion Self-Regenerating Suppressor, recycle mode, 223 ma Safety Warnings Mercury salts and organic mercury compounds are very toxic and sometimes can be fatal. Additionally, perchlorate used in the eluent is classified as a hazardous chemical because it interferes with iodide uptake thereby causing hypothyroidism. Review material safety data sheets for handling precautions, safe storage, and disposal methods, and review local regulations prior to ordering reagents or analyzing samples. Thermo Scientific Poster Note PN70284_E 09/12S 3

Results Method 1: Ion Pairing The mercury species is separated as a mercury-cysteine complex by ion pair chromatography using the cysteine perchlorate-based mobile phase on the mixed mode Dionex IonPac CS5A column. The Dionex IonPac CS5A has both anion- and cation-exchange properties making it ideal for the separation of transition metal species. As the analytes elute from the column, they are detected by UV at 210 nm. All three mercury species evaluated had linear responses replicate injections of four standards from 1 to 10 mg/l with concentration (r 2 > 0.999). The ground samples were extracted with eluent to ensure that the ions were soluble throughout the chromatographic separation. Figure 2 shows the separation of methymercury and inorganic mercury standards. The chromatograms show that inorganic mercury (Hg 2+ ) is well resolved from methylmercury. Ethylmercury is not shown. FIGURE 2. Separation of mercury standards. Column: Dionex IonPac CG5A, CS5A, 45 4 mm Eluent: 1 mm Acetic acid, 1 mm Sodium perchlorate, 5 mm Cysteine, ph 4 Flow Rate: 1.75 ml/min mau Column Temp.: 30 C 1 Detection: UV Absorbance, 210 nm 2 Inj. Volume: 25 µl B A Preparation: A: Deionized water B: Methanol, working standards -5 diluted in deionized water 0 5 10 15 18 Peaks: 1.Hg 2+ 2.5 mg/l 2. Methylmercury 9.3 Figure 3 shows the separation of inorganic and organic mercury in dietary supplement 1 after extraction in 20 ml of the acetic acid, sodium perchlorate, and cysteine eluent. This sample has moderately high concentrations of inorganic mercury as compared with the other four samples. No methylmercury or ethylmercury was detected. FIGURE 3. Determination of organic and inorganic mercury in dietary supplement Number 1. 50 mau 1-10 0 5 10 Minutes 15 18 Column: Dionex IonPac CG5A, CS5A, 4 mm Eluent: 1 mm Acetic acid, 1 mm Sodium perchlorate, 5 mm Cysteine, ph 4 Flow Rate: 1.75 ml/min Column Temp.: 30 C Detection: UV Absorbance, 210 nm Inj. Volume: 25 µl Sample Prep.: 1:5 dilution with deionized water Peaks: 1. Total Hg 2+ 3.69 mg/l 52 µg/tablet 0.0586 wt% 4 Mercury Speciation Determinations in Asian Dietary Supplements

The results of the mercury speciation determinations are summarized in Table 1. Sample 2 had the highest concentration and sample 1 the lowest. Only very high concentrations of inorganic mercury were found; no organic mercury was detected. Although the results are very high (400 to 2200 mg/kg), the effect could be more devastating if ethylmercury and methylmercury were present at these concentrations. Table 1. Summary of mercury speciation determinations. Sample Measured (mg/l) Inorganic Mercury Calculated (wt %) Calculated (µg/tablet) Methylmercury / Ethylmercury Control -- -- -- -- 1 3.69 0.0586 52 ND 2 15.6 0.2265 387 ND 3 4.82 0.0437 117 ND 4 5.31 0.0473 123 ND 5 11.3 0.0708 243 ND Method 2: Counter Anion Determinations Counter anion determinations were needed to conduct a mass balance of the mercury speciation in the dietary supplement samples. We selected the high capacity Dionex IonPac AS11-HC anion-exchange column optimized for organic acid determinations for this application because this column provides the best separations when the samples are uncharacterized. Inorganic anions and organic acids in these samples were separated using a shallow potassium hydroxide gradient to resolve as many peaks as possible. The eluent was electrolytically generated without solution preparation by just adding water. The chromatographic separation of a water extract from Sample 5 is shown in Figure 4. The sample has high amounts of chloride and sulfate (~ 700 mg/kg) with < 50 mg/kg of nitrate, oxalate, phosphate, and citrate. FIGURE 4: Determinations of inorganic anions and organic acids in a water extract of dietary supplement Number 5. 20 µs 1 2 3 6 45 7 8 Columns: Dionex IonPac AG11-HC, AS11-HC, 4 mm Eluent Source: Dionex EGC III KOH Gradient: 1 mm from 0 8 min, 1 15 mm from 8 18 min, 15 30 mm from 18 28 min, 30 60 mm from 28 38 min Temperature: 30 C Flow Rate: 1.5 ml/min Inj. Volume: 25 µl Detection: Suppressed conductivity, Dionex ASRS 300, 4 mm, recycle mode Sample Prep.: 5 min extraction in deionized water, settle 5 min, filter, dilute 1:5 total wt % Peaks: 1. Acetate 2. Formate 10 9-2 0 10 20 30 35 Minutes 3. Chloride 0.716 4. Bromide 5. Nitrate 0.142 6. Carbonate 7. Sulfate 0.662 8. Oxalate 0.043 9. Phosphate 0.025 10. Citrate 0.039 Thermo Scientific Poster Note PN70284_E 09/12S 5

The counter anions results are summarized in Table 2. The counter anions are primarily chloride and sulfate. Sample 2 has the highest results. Table 2. Summary of counter anion results. Counter Anion Sample # (wt %) 1 2 3 4 5 Acetate 0.012 0.389 0.014 0.008 -- Formate 0.002 0.019 -- -- -- Chloride 0.080 1.624 0.128 0.254 0.716 Bromide -- -- 0.093 0.192 -- Nitrate 0.102 0.507 0.061 0.201 0.142 Sulfate 0.240 1.818 0.196 0.554 0.662 Oxalate 0.003 0.026 0.005 0.011 0.043 Phosphate -- 0.005 -- 0.070 0.025 Citrate -- 0.050 0.018 0.042 0.039 Conclusion These tests identified that the majority of the soluble mercury in the dietary supplements was inorganic mercury (Hg 2+ ), corresponding to the sub-percent amounts found in the patients. IC with Inductively Coupled Plasma (ICP) provides a total solution by combining speciation with total elemental content. ICP analysis screens samples for unknown metal contamination especially when only one species is present, but also provides the total amount of an element when more than one species is present. IC analysis separates metal species thereby providing important mercury speciation when multiple species are present. Mercury speciation determinations define the potential toxicity in food sources. Inorganic anions and organic acids needed for mass balance calculations are easily and accurately determined by anion-exchange chromatography with a Reagent-Free IC system. For more information on this method and mercury analysis methods, see references 1 4. References 1. Sarzanini, C.; Sacchero, G.; Aceto, M.; Aboilino, O.; Mentasti, Ed. Ion Chromatographic Separation and On-Line Cold Vapour Atomic Absorption Spectrometric Determination of Methylmercury, Ethylmercury and Inorganic Mercury, Anal. Chim. Acta, 1993, 00, 1 7. 2. Dickson, H.R; Price, R. Application Note AN40992 Accurate Analysis of Low Levels of Mercury in Fish by Vapor Generation AA, Thermo Fisher Scientific, Cambridge, UK, 2010. 3. Christison, T.; Hoefler, F.; Lopez, L. Application Note AN43130 Combining the Synergies of Ion Chromatography and Inductively Coupled Plasma to Identify Mercury Contamination in Herbal Medicines, Thermo Fisher Scientific, Sunnyvale, CA, 2012. 4. Dionex Application Note AN 131, Determination of Transition Metals at PPT Levels in High Purity Water and SC-2 (D-Clean) Baths, LPN 1058, Thermo Fisher Scientific, Sunnyvale, CA, 1998. For research purposes only, not for clinical diagnostics. 6 Mercury Speciation Determinations in Asian Dietary Supplements

www.thermofisher.com/dionex 2016 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific Inc. and its subsidiaries. This information is presented as an example of the capabilities of Thermo Fisher Scientific Inc. products. It is not intended to encourage use of these products in any manners that might infringe the intellectual property rights of others. Specifications, terms and pricing are subject to change. Not all products are available in all countries. Please consult your local sales representative for details. Australia +61 3 9757 4486 Austria +43 1 616 51 25 Benelux +31 20 683 9768 +32 3 353 42 94 Brazil +55 11 3731 5140 China +852 2428 3282 Denmark +45 36 36 90 90 France +33 1 39 30 01 10 Germany +49 6126 991 0 India +91 22 2764 2735 Ireland +353 1 644 0064 Italy +39 02 51 62 1267 Japan +81 6 6885 1213 Korea +82 2 3420 8600 Singapore +65 6289 1190 Sweden +46 8 473 3380 Switzerland +41 62 205 9966 Taiwan +886 2 8751 6655 UK +44 1276 691722 USA and Canada +847 295 7500 PN70284_E 08/16S