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Standardization of microcystin extraction from fish tissues: A novel internal standard as a surrogate for polar and non-polar variants
Microcystins (MCs), a class of potent liver/hepatopancreatic toxins produced by numerous species of freshwater cyanobacteria, are well known for their toxic effects on aquatic organisms and humans. The extraction efficiencies of MCs can vary greatly as a result of matrix differences and/or differenc...
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Published in: | Toxicon (Oxford) 2009-02, Vol.53 (2), p.238-245 |
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description | Microcystins (MCs), a class of potent liver/hepatopancreatic toxins produced by numerous species of freshwater cyanobacteria, are well known for their toxic effects on aquatic organisms and humans. The extraction efficiencies of MCs can vary greatly as a result of matrix differences and/or differences in the extraction solvents, techniques, and clean-up steps utilized. Here we report the preparation of a unique internal standard, (S-hydroxypropyl-cys
7)microcystin-LR (thiol-LR), with a mass different than any known MCs, which can be spiked into field samples and quantified via HPLC-MS along with endogenous MCs. Thiol-LR is modified at the Mdha residue, and therefore, provides an accurate measure of only free MCs that are not covalently bound to endogenous thiols in the matrix. The internal standard proved to be a good surrogate for MC-RR, -LR, and -LA in fish liver tissue. In fish muscle tissue, thiol-LR was a good surrogate for polar variants, MC-RR and -LR, but was less representative of the non-polar variant, MC-LA. Coupling of the internal standard (8
μg/g ww tissue) with HPLC-MS detection will standardize the quantification of free microcystins across species, tissue types, and extraction methods, making the estimation of exposure risk more reliable. |
doi_str_mv | 10.1016/j.toxicon.2008.11.007 |
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7)microcystin-LR (thiol-LR), with a mass different than any known MCs, which can be spiked into field samples and quantified via HPLC-MS along with endogenous MCs. Thiol-LR is modified at the Mdha residue, and therefore, provides an accurate measure of only free MCs that are not covalently bound to endogenous thiols in the matrix. The internal standard proved to be a good surrogate for MC-RR, -LR, and -LA in fish liver tissue. In fish muscle tissue, thiol-LR was a good surrogate for polar variants, MC-RR and -LR, but was less representative of the non-polar variant, MC-LA. Coupling of the internal standard (8
μg/g ww tissue) with HPLC-MS detection will standardize the quantification of free microcystins across species, tissue types, and extraction methods, making the estimation of exposure risk more reliable.</description><identifier>ISSN: 0041-0101</identifier><identifier>EISSN: 1879-3150</identifier><identifier>DOI: 10.1016/j.toxicon.2008.11.007</identifier><identifier>PMID: 19063912</identifier><identifier>CODEN: TOXIA6</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Animal poisons toxicology. Antivenoms ; Animals ; Bacteriology ; Biological and medical sciences ; Chromatography, High Pressure Liquid - methods ; Cyanophyta ; Fish ; Fishes - metabolism ; Fresh Water ; Freshwater ; Fundamental and applied biological sciences. Psychology ; Geologic Sediments ; HPLC-MS ; Internal standard ; Mass Spectrometry - methods ; Medical sciences ; MeOH extraction ; Microbiology ; Microcystins ; Microcystins - chemistry ; Molecular Structure ; Muscle, Skeletal - chemistry ; Muscle, Skeletal - metabolism ; Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains ; Sediments ; Thiol-LR ; Time Factors ; Toxicology</subject><ispartof>Toxicon (Oxford), 2009-02, Vol.53 (2), p.238-245</ispartof><rights>2008 Elsevier Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-224ed5481145bee42c13b32bb0ab9e6e02c01e2aada67b1d3a3d81c9824ce11b3</citedby><cites>FETCH-LOGICAL-c424t-224ed5481145bee42c13b32bb0ab9e6e02c01e2aada67b1d3a3d81c9824ce11b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21139349$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19063912$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, Juliette L.</creatorcontrib><creatorcontrib>Boyer, Gregory L.</creatorcontrib><title>Standardization of microcystin extraction from fish tissues: A novel internal standard as a surrogate for polar and non-polar variants</title><title>Toxicon (Oxford)</title><addtitle>Toxicon</addtitle><description>Microcystins (MCs), a class of potent liver/hepatopancreatic toxins produced by numerous species of freshwater cyanobacteria, are well known for their toxic effects on aquatic organisms and humans. The extraction efficiencies of MCs can vary greatly as a result of matrix differences and/or differences in the extraction solvents, techniques, and clean-up steps utilized. Here we report the preparation of a unique internal standard, (S-hydroxypropyl-cys
7)microcystin-LR (thiol-LR), with a mass different than any known MCs, which can be spiked into field samples and quantified via HPLC-MS along with endogenous MCs. Thiol-LR is modified at the Mdha residue, and therefore, provides an accurate measure of only free MCs that are not covalently bound to endogenous thiols in the matrix. The internal standard proved to be a good surrogate for MC-RR, -LR, and -LA in fish liver tissue. In fish muscle tissue, thiol-LR was a good surrogate for polar variants, MC-RR and -LR, but was less representative of the non-polar variant, MC-LA. Coupling of the internal standard (8
μg/g ww tissue) with HPLC-MS detection will standardize the quantification of free microcystins across species, tissue types, and extraction methods, making the estimation of exposure risk more reliable.</description><subject>Animal poisons toxicology. Antivenoms</subject><subject>Animals</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Cyanophyta</subject><subject>Fish</subject><subject>Fishes - metabolism</subject><subject>Fresh Water</subject><subject>Freshwater</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Geologic Sediments</subject><subject>HPLC-MS</subject><subject>Internal standard</subject><subject>Mass Spectrometry - methods</subject><subject>Medical sciences</subject><subject>MeOH extraction</subject><subject>Microbiology</subject><subject>Microcystins</subject><subject>Microcystins - chemistry</subject><subject>Molecular Structure</subject><subject>Muscle, Skeletal - chemistry</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</subject><subject>Sediments</subject><subject>Thiol-LR</subject><subject>Time Factors</subject><subject>Toxicology</subject><issn>0041-0101</issn><issn>1879-3150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi0EotvCI4B8obcEj-1kEy6oqiggVeIAnK2JMwGvEnuxvauWB-C5cdkIjpxG1nz_zPj_GXsBogYB7etdncOds8HXUoiuBqiF2D5iG-i2faWgEY_ZRggNlSj4GTtPaSeEUF3fPmVn0ItW9SA37NfnjH7EOLqfmF3wPEx8cTYGe5-y85zuckT7pzPFsPDJpe88u5QOlN7wK-7DkWbufKboceZpncYxceTpEGP4hpn4FCLfhxkjL_0i8tXpdcTo0Of0jD2ZcE70fK0X7OvNuy_XH6rbT-8_Xl_dVlZLnSspNY2N7gB0MxBpaUENSg6DwKGnloS0AkgijthuBxgVqrED23dSWwIY1AW7PM3dx_CjfCGbxSVL84yewiEZKWSjWqUL2JzAYkVKkSazj27BeG9AmIcAzM6sAZiHAAyAKQEU3ct1wWFYaPynWh0vwKsVwGRxniJ669JfTgKoXum-cG9PHBU7jo6iSdaRtzS6SDabMbj_nPIbqj6qIA</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Smith, Juliette L.</creator><creator>Boyer, Gregory L.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope></search><sort><creationdate>20090201</creationdate><title>Standardization of microcystin extraction from fish tissues: A novel internal standard as a surrogate for polar and non-polar variants</title><author>Smith, Juliette L. ; Boyer, Gregory L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-224ed5481145bee42c13b32bb0ab9e6e02c01e2aada67b1d3a3d81c9824ce11b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animal poisons toxicology. 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Psychology</topic><topic>Geologic Sediments</topic><topic>HPLC-MS</topic><topic>Internal standard</topic><topic>Mass Spectrometry - methods</topic><topic>Medical sciences</topic><topic>MeOH extraction</topic><topic>Microbiology</topic><topic>Microcystins</topic><topic>Microcystins - chemistry</topic><topic>Molecular Structure</topic><topic>Muscle, Skeletal - chemistry</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</topic><topic>Sediments</topic><topic>Thiol-LR</topic><topic>Time Factors</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Juliette L.</creatorcontrib><creatorcontrib>Boyer, Gregory L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Toxicon (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Juliette L.</au><au>Boyer, Gregory L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Standardization of microcystin extraction from fish tissues: A novel internal standard as a surrogate for polar and non-polar variants</atitle><jtitle>Toxicon (Oxford)</jtitle><addtitle>Toxicon</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>53</volume><issue>2</issue><spage>238</spage><epage>245</epage><pages>238-245</pages><issn>0041-0101</issn><eissn>1879-3150</eissn><coden>TOXIA6</coden><abstract>Microcystins (MCs), a class of potent liver/hepatopancreatic toxins produced by numerous species of freshwater cyanobacteria, are well known for their toxic effects on aquatic organisms and humans. The extraction efficiencies of MCs can vary greatly as a result of matrix differences and/or differences in the extraction solvents, techniques, and clean-up steps utilized. Here we report the preparation of a unique internal standard, (S-hydroxypropyl-cys
7)microcystin-LR (thiol-LR), with a mass different than any known MCs, which can be spiked into field samples and quantified via HPLC-MS along with endogenous MCs. Thiol-LR is modified at the Mdha residue, and therefore, provides an accurate measure of only free MCs that are not covalently bound to endogenous thiols in the matrix. The internal standard proved to be a good surrogate for MC-RR, -LR, and -LA in fish liver tissue. In fish muscle tissue, thiol-LR was a good surrogate for polar variants, MC-RR and -LR, but was less representative of the non-polar variant, MC-LA. Coupling of the internal standard (8
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subjects | Animal poisons toxicology. Antivenoms Animals Bacteriology Biological and medical sciences Chromatography, High Pressure Liquid - methods Cyanophyta Fish Fishes - metabolism Fresh Water Freshwater Fundamental and applied biological sciences. Psychology Geologic Sediments HPLC-MS Internal standard Mass Spectrometry - methods Medical sciences MeOH extraction Microbiology Microcystins Microcystins - chemistry Molecular Structure Muscle, Skeletal - chemistry Muscle, Skeletal - metabolism Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains Sediments Thiol-LR Time Factors Toxicology |
title | Standardization of microcystin extraction from fish tissues: A novel internal standard as a surrogate for polar and non-polar variants |
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