The determination of methylmercury in biological samples by HPLC coupled to ICP-MS detection
The use of high‐performance liquid chromatography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. Analysis of these sample types is required when carrying out biomonitoring studies to...
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description | The use of high‐performance liquid chromatography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. Analysis of these sample types is required when carrying out biomonitoring studies to determine human dietary exposure to this toxic mercurial compound. The developed method used a mobile phase containing an organic modifier and a sulfydryl compound (1:1 v/v methanol:water containing 0.01% v/v 2‐mercaptoethanol) to limit peak tailing and aid separation. The chromatographic separation was coupled to the ICP‐MS detector via a short piece of PEEK tubing, attached to the nebulizer. A cooled spraychamber and oxygen addition post‐nebulization were required to limit the solvent loading on the plasma and reduce carbon build‐up on the cones, respectively. The sample preparation procedure employed a drying step followed by digestion of the sample using tetramethylammonium hydroxide (TMAH) and heating in an open vessel microwave system. Two fish tissue certified reference materials (CRM), tuna fish CRM 463 and 464 (BCR, Brussels), a tuna fish proficiency test sample, IMEP‐20 (IRMM, Geel, Belgium) and a hair CRM NIES no. 13 (National Institute of Environmental Science, Japan), were used to evaluate the method. The recovery of MeHg+ for these four materials was between 83 and 100%, with precisions better than 6% for three separate extractions of the different materials. The limit of quantitation for MeHg+ using the developed protocol was 0.5 µg Hg g−1. The stability of MeHg+ in the fish sample extracts was also assessed and losses of 14–16% were observed after storage of the extracts in a refrigerator at 5 °C, in high‐density polypropylene tubes, for 6 months. The developed protocol has been used previously with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high accuracy quantitation. Copyright © 2006 John Wiley & Sons, Ltd.
The use of high performance liquid chro‐matography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. The developed protocol can be used with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high ac |
doi_str_mv | 10.1002/aoc.1173 |
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The use of high performance liquid chro‐matography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. The developed protocol can be used with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high accuracy quantitation of MeHg+ in biological samples used in biomonitoring studies.</description><identifier>ISSN: 0268-2605</identifier><identifier>EISSN: 1099-0739</identifier><identifier>DOI: 10.1002/aoc.1173</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>biomonitoring ; elemental speciation ; fish tissue ; hair ; HPLC-ICP-MS ; methylmercury</subject><ispartof>Applied organometallic chemistry, 2007-05, Vol.21 (5), p.303-310</ispartof><rights>Copyright © 2006 John Wiley & Sons, Ltd. John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3343-17c79d0bc026b3e72e8c7e791f9ca143775d26eec2c5bff3c4f490a093abb1fc3</citedby><cites>FETCH-LOGICAL-c3343-17c79d0bc026b3e72e8c7e791f9ca143775d26eec2c5bff3c4f490a093abb1fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Faoc.1173$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Faoc.1173$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Vidler, Daniel S.</creatorcontrib><creatorcontrib>Jenkins, Richard O.</creatorcontrib><creatorcontrib>Hall, John F.</creatorcontrib><creatorcontrib>Harrington, Chris F.</creatorcontrib><title>The determination of methylmercury in biological samples by HPLC coupled to ICP-MS detection</title><title>Applied organometallic chemistry</title><addtitle>Appl. Organometal. Chem</addtitle><description>The use of high‐performance liquid chromatography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. Analysis of these sample types is required when carrying out biomonitoring studies to determine human dietary exposure to this toxic mercurial compound. The developed method used a mobile phase containing an organic modifier and a sulfydryl compound (1:1 v/v methanol:water containing 0.01% v/v 2‐mercaptoethanol) to limit peak tailing and aid separation. The chromatographic separation was coupled to the ICP‐MS detector via a short piece of PEEK tubing, attached to the nebulizer. A cooled spraychamber and oxygen addition post‐nebulization were required to limit the solvent loading on the plasma and reduce carbon build‐up on the cones, respectively. The sample preparation procedure employed a drying step followed by digestion of the sample using tetramethylammonium hydroxide (TMAH) and heating in an open vessel microwave system. Two fish tissue certified reference materials (CRM), tuna fish CRM 463 and 464 (BCR, Brussels), a tuna fish proficiency test sample, IMEP‐20 (IRMM, Geel, Belgium) and a hair CRM NIES no. 13 (National Institute of Environmental Science, Japan), were used to evaluate the method. The recovery of MeHg+ for these four materials was between 83 and 100%, with precisions better than 6% for three separate extractions of the different materials. The limit of quantitation for MeHg+ using the developed protocol was 0.5 µg Hg g−1. The stability of MeHg+ in the fish sample extracts was also assessed and losses of 14–16% were observed after storage of the extracts in a refrigerator at 5 °C, in high‐density polypropylene tubes, for 6 months. The developed protocol has been used previously with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high accuracy quantitation. Copyright © 2006 John Wiley & Sons, Ltd.
The use of high performance liquid chro‐matography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. The developed protocol can be used with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high accuracy quantitation of MeHg+ in biological samples used in biomonitoring studies.</description><subject>biomonitoring</subject><subject>elemental speciation</subject><subject>fish tissue</subject><subject>hair</subject><subject>HPLC-ICP-MS</subject><subject>methylmercury</subject><issn>0268-2605</issn><issn>1099-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp10M1KxDAUBeAgCo4_4CNkJW6qSdMmZinFGcVRBx0VRAhpeqvRthmTFu3b23FEcOHqcuHjcDgI7VFySAmJj7Qzh5QKtoZGlEgZEcHkOhqRmB9HMSfpJtoK4ZUQIjlNRuhp_gK4gBZ8bRvdWtdgV-Ia2pe-qsGbzvfYNji3rnLP1ugKB10vKgg47_HZbJph47rhL3Dr8Hk2iy5vv-PMMmoHbZS6CrD7c7fR3fh0np1F0-vJeXYyjQxjCYuoMEIWJDdDyZyBiOHYCBCSltJomjAh0iLmACY2aV6WzCRlIokmkuk8p6Vh22h_lbvw7r2D0KraBgNVpRtwXVCx5CnnnAzwYAWNdyF4KNXC21r7XlGilvOpYT61nG-g0Yp-2Ar6f506uc7-ehta-Pz12r8pLphI1cPVRM0niby5f7xQY_YFvGuAkA</recordid><startdate>200705</startdate><enddate>200705</enddate><creator>Vidler, Daniel S.</creator><creator>Jenkins, Richard O.</creator><creator>Hall, John F.</creator><creator>Harrington, Chris F.</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>200705</creationdate><title>The determination of methylmercury in biological samples by HPLC coupled to ICP-MS detection</title><author>Vidler, Daniel S. ; Jenkins, Richard O. ; Hall, John F. ; Harrington, Chris F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3343-17c79d0bc026b3e72e8c7e791f9ca143775d26eec2c5bff3c4f490a093abb1fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>biomonitoring</topic><topic>elemental speciation</topic><topic>fish tissue</topic><topic>hair</topic><topic>HPLC-ICP-MS</topic><topic>methylmercury</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vidler, Daniel S.</creatorcontrib><creatorcontrib>Jenkins, Richard O.</creatorcontrib><creatorcontrib>Hall, John F.</creatorcontrib><creatorcontrib>Harrington, Chris F.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied organometallic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vidler, Daniel S.</au><au>Jenkins, Richard O.</au><au>Hall, John F.</au><au>Harrington, Chris F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The determination of methylmercury in biological samples by HPLC coupled to ICP-MS detection</atitle><jtitle>Applied organometallic chemistry</jtitle><addtitle>Appl. Organometal. Chem</addtitle><date>2007-05</date><risdate>2007</risdate><volume>21</volume><issue>5</issue><spage>303</spage><epage>310</epage><pages>303-310</pages><issn>0268-2605</issn><eissn>1099-0739</eissn><abstract>The use of high‐performance liquid chromatography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. Analysis of these sample types is required when carrying out biomonitoring studies to determine human dietary exposure to this toxic mercurial compound. The developed method used a mobile phase containing an organic modifier and a sulfydryl compound (1:1 v/v methanol:water containing 0.01% v/v 2‐mercaptoethanol) to limit peak tailing and aid separation. The chromatographic separation was coupled to the ICP‐MS detector via a short piece of PEEK tubing, attached to the nebulizer. A cooled spraychamber and oxygen addition post‐nebulization were required to limit the solvent loading on the plasma and reduce carbon build‐up on the cones, respectively. The sample preparation procedure employed a drying step followed by digestion of the sample using tetramethylammonium hydroxide (TMAH) and heating in an open vessel microwave system. Two fish tissue certified reference materials (CRM), tuna fish CRM 463 and 464 (BCR, Brussels), a tuna fish proficiency test sample, IMEP‐20 (IRMM, Geel, Belgium) and a hair CRM NIES no. 13 (National Institute of Environmental Science, Japan), were used to evaluate the method. The recovery of MeHg+ for these four materials was between 83 and 100%, with precisions better than 6% for three separate extractions of the different materials. The limit of quantitation for MeHg+ using the developed protocol was 0.5 µg Hg g−1. The stability of MeHg+ in the fish sample extracts was also assessed and losses of 14–16% were observed after storage of the extracts in a refrigerator at 5 °C, in high‐density polypropylene tubes, for 6 months. The developed protocol has been used previously with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high accuracy quantitation. Copyright © 2006 John Wiley & Sons, Ltd.
The use of high performance liquid chro‐matography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. The developed protocol can be used with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high accuracy quantitation of MeHg+ in biological samples used in biomonitoring studies.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/aoc.1173</doi><tpages>8</tpages></addata></record> |
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subjects | biomonitoring elemental speciation fish tissue hair HPLC-ICP-MS methylmercury |
title | The determination of methylmercury in biological samples by HPLC coupled to ICP-MS detection |
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