Liquid chromatographic method development for anabolic androgenic steroids using a monolithic column Application to animal feed samples
An isocratic HPLC method for the determination with screening purposes of anabolic androgenic steroids (AASs: fluoxymesterone, boldenone, nortestosterone, metandrostenolone, norethindrone, methyltestosterone and bolasterone), used as growth promoting agents, in finishing pig feed samples has been de...
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Veröffentlicht in: | Analytica chimica acta 2008-03, Vol.611 (1), p.103-112 |
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description | An isocratic HPLC method for the determination with screening purposes of anabolic androgenic steroids (AASs: fluoxymesterone, boldenone, nortestosterone, metandrostenolone, norethindrone, methyltestosterone and bolasterone), used as growth promoting agents, in finishing pig feed samples has been developed and validated. The separation was achieved by using a reversed-phase Chromolith RP-18e column at controlled temperature, UV-detection at 245nm and epitestosterone as internal standard. The method development involved optimization of different aqueous-organic mobile phases using methanol or acetonitrile as organic modifiers, flow-rate and temperature. The optimum separation for these compounds was achieved at 40 degrees C using ultrapure water:acetonitrile (71:29, v/v) as mobile phase and 3mLmin(-1) flow-rate, allowing the separation of AASs with baseline resolution in about 15min. The optimized method was applied to the analysis of AASs in finishing pig feed samples. Prior to HPLC, sample preparation procedure was used by leaching using acetonitrile, saponification in a basic medium and solid-phase extraction using polymeric Abselut Nexus cartridges. Method validation has been carried out according to the European Commission Decision 2002/657/EC. The extraction efficiencies, decision limits (CCalpha) and detection capabilities (CCbeta) for these compounds were in the range 83-96%, 27-37 and 32-47microgkg(-1) range, respectively. The within-laboratory reproducibility at 1, 1.5 and 2 CCbeta concentration levels were smaller than 13, 10 and 8%, respectively. Finally, the proposed method was successfully applied to nine different kinds of animal feed. |
doi_str_mv | 10.1016/j.aca.2008.01.057 |
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The separation was achieved by using a reversed-phase Chromolith RP-18e column at controlled temperature, UV-detection at 245nm and epitestosterone as internal standard. The method development involved optimization of different aqueous-organic mobile phases using methanol or acetonitrile as organic modifiers, flow-rate and temperature. The optimum separation for these compounds was achieved at 40 degrees C using ultrapure water:acetonitrile (71:29, v/v) as mobile phase and 3mLmin(-1) flow-rate, allowing the separation of AASs with baseline resolution in about 15min. The optimized method was applied to the analysis of AASs in finishing pig feed samples. Prior to HPLC, sample preparation procedure was used by leaching using acetonitrile, saponification in a basic medium and solid-phase extraction using polymeric Abselut Nexus cartridges. Method validation has been carried out according to the European Commission Decision 2002/657/EC. The extraction efficiencies, decision limits (CCalpha) and detection capabilities (CCbeta) for these compounds were in the range 83-96%, 27-37 and 32-47microgkg(-1) range, respectively. The within-laboratory reproducibility at 1, 1.5 and 2 CCbeta concentration levels were smaller than 13, 10 and 8%, respectively. Finally, the proposed method was successfully applied to nine different kinds of animal feed.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2008.01.057</identifier><identifier>PMID: 18298974</identifier><identifier>CODEN: ACACAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier</publisher><subject>Anabolic Agents - analysis ; Analytical chemistry ; Androgens - analysis ; Animal Feed - analysis ; Calibration ; Chemistry ; Chromatographic methods and physical methods associated with chromatography ; Chromatography, High Pressure Liquid - instrumentation ; Chromatography, High Pressure Liquid - methods ; Exact sciences and technology ; Other chromatographic methods ; Reproducibility of Results ; Sensitivity and Specificity ; Tandem Mass Spectrometry</subject><ispartof>Analytica chimica acta, 2008-03, Vol.611 (1), p.103-112</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20144545$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18298974$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MUNIZ-VALENCIA, R</creatorcontrib><creatorcontrib>GONZALO-LUMBRERAS, R</creatorcontrib><creatorcontrib>SANTOS-MONTES, A</creatorcontrib><creatorcontrib>IZQUIERDO-HORNILLOS, R</creatorcontrib><title>Liquid chromatographic method development for anabolic androgenic steroids using a monolithic column Application to animal feed samples</title><title>Analytica chimica acta</title><addtitle>Anal Chim Acta</addtitle><description>An isocratic HPLC method for the determination with screening purposes of anabolic androgenic steroids (AASs: fluoxymesterone, boldenone, nortestosterone, metandrostenolone, norethindrone, methyltestosterone and bolasterone), used as growth promoting agents, in finishing pig feed samples has been developed and validated. The separation was achieved by using a reversed-phase Chromolith RP-18e column at controlled temperature, UV-detection at 245nm and epitestosterone as internal standard. The method development involved optimization of different aqueous-organic mobile phases using methanol or acetonitrile as organic modifiers, flow-rate and temperature. The optimum separation for these compounds was achieved at 40 degrees C using ultrapure water:acetonitrile (71:29, v/v) as mobile phase and 3mLmin(-1) flow-rate, allowing the separation of AASs with baseline resolution in about 15min. The optimized method was applied to the analysis of AASs in finishing pig feed samples. Prior to HPLC, sample preparation procedure was used by leaching using acetonitrile, saponification in a basic medium and solid-phase extraction using polymeric Abselut Nexus cartridges. Method validation has been carried out according to the European Commission Decision 2002/657/EC. The extraction efficiencies, decision limits (CCalpha) and detection capabilities (CCbeta) for these compounds were in the range 83-96%, 27-37 and 32-47microgkg(-1) range, respectively. The within-laboratory reproducibility at 1, 1.5 and 2 CCbeta concentration levels were smaller than 13, 10 and 8%, respectively. Finally, the proposed method was successfully applied to nine different kinds of animal feed.</description><subject>Anabolic Agents - analysis</subject><subject>Analytical chemistry</subject><subject>Androgens - analysis</subject><subject>Animal Feed - analysis</subject><subject>Calibration</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Chromatography, High Pressure Liquid - instrumentation</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Exact sciences and technology</subject><subject>Other chromatographic methods</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Tandem Mass Spectrometry</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1uFDEQhC0EIpvAA3BBvsBtBv979hhFgSCtxAXOqx7bs-vIPxPbg8QT8NoYsXDl1N3qr0qqQugNJSMlVH14HMHAyAiZRkJHIvUztKOT5oPgTDxHO0IIH5jS5Apd1_rYT0aJeImu6MT2016LHfp58E-bt9icS47Q8qnAevYGR9fO2WLrvruQ1-hSw0suGBLMOfQ_JFvyyaW-1uZK9rbirfp0woBjTp1pv21MDltM-HZduwiazwm33MU-QsCLcxZXiGtw9RV6sUCo7vVl3qBvH--_3j0Mhy-fPt_dHoaVadIGZYAqUEIqMTMnpTUzZcTArKUFZRS3ZhJuYUZLZywYwxbOhWWG7rkVE-M36P0f37Xkp83Vdoy-GhcCJJe3etSE872U_L9gb5hSxXUH317AbY7OHtfSw5Ufx78dd-DdBYBqICwFkvH1H8cIFUIKyX8BOsCPiA</recordid><startdate>20080317</startdate><enddate>20080317</enddate><creator>MUNIZ-VALENCIA, R</creator><creator>GONZALO-LUMBRERAS, R</creator><creator>SANTOS-MONTES, A</creator><creator>IZQUIERDO-HORNILLOS, R</creator><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>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20080317</creationdate><title>Liquid chromatographic method development for anabolic androgenic steroids using a monolithic column Application to animal feed samples</title><author>MUNIZ-VALENCIA, R ; GONZALO-LUMBRERAS, R ; SANTOS-MONTES, A ; IZQUIERDO-HORNILLOS, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p270t-6ca16a64564b2e55dcb120cab75da6c63dc84ef2c75ecdacc2f334d2c193d4823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Anabolic Agents - analysis</topic><topic>Analytical chemistry</topic><topic>Androgens - analysis</topic><topic>Animal Feed - analysis</topic><topic>Calibration</topic><topic>Chemistry</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Chromatography, High Pressure Liquid - instrumentation</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Exact sciences and technology</topic><topic>Other chromatographic methods</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Tandem Mass Spectrometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MUNIZ-VALENCIA, R</creatorcontrib><creatorcontrib>GONZALO-LUMBRERAS, R</creatorcontrib><creatorcontrib>SANTOS-MONTES, A</creatorcontrib><creatorcontrib>IZQUIERDO-HORNILLOS, R</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>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MUNIZ-VALENCIA, R</au><au>GONZALO-LUMBRERAS, R</au><au>SANTOS-MONTES, A</au><au>IZQUIERDO-HORNILLOS, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liquid chromatographic method development for anabolic androgenic steroids using a monolithic column Application to animal feed samples</atitle><jtitle>Analytica chimica acta</jtitle><addtitle>Anal Chim Acta</addtitle><date>2008-03-17</date><risdate>2008</risdate><volume>611</volume><issue>1</issue><spage>103</spage><epage>112</epage><pages>103-112</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><coden>ACACAM</coden><abstract>An isocratic HPLC method for the determination with screening purposes of anabolic androgenic steroids (AASs: fluoxymesterone, boldenone, nortestosterone, metandrostenolone, norethindrone, methyltestosterone and bolasterone), used as growth promoting agents, in finishing pig feed samples has been developed and validated. The separation was achieved by using a reversed-phase Chromolith RP-18e column at controlled temperature, UV-detection at 245nm and epitestosterone as internal standard. The method development involved optimization of different aqueous-organic mobile phases using methanol or acetonitrile as organic modifiers, flow-rate and temperature. The optimum separation for these compounds was achieved at 40 degrees C using ultrapure water:acetonitrile (71:29, v/v) as mobile phase and 3mLmin(-1) flow-rate, allowing the separation of AASs with baseline resolution in about 15min. The optimized method was applied to the analysis of AASs in finishing pig feed samples. Prior to HPLC, sample preparation procedure was used by leaching using acetonitrile, saponification in a basic medium and solid-phase extraction using polymeric Abselut Nexus cartridges. Method validation has been carried out according to the European Commission Decision 2002/657/EC. The extraction efficiencies, decision limits (CCalpha) and detection capabilities (CCbeta) for these compounds were in the range 83-96%, 27-37 and 32-47microgkg(-1) range, respectively. The within-laboratory reproducibility at 1, 1.5 and 2 CCbeta concentration levels were smaller than 13, 10 and 8%, respectively. Finally, the proposed method was successfully applied to nine different kinds of animal feed.</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><pmid>18298974</pmid><doi>10.1016/j.aca.2008.01.057</doi><tpages>10</tpages></addata></record> |
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subjects | Anabolic Agents - analysis Analytical chemistry Androgens - analysis Animal Feed - analysis Calibration Chemistry Chromatographic methods and physical methods associated with chromatography Chromatography, High Pressure Liquid - instrumentation Chromatography, High Pressure Liquid - methods Exact sciences and technology Other chromatographic methods Reproducibility of Results Sensitivity and Specificity Tandem Mass Spectrometry |
title | Liquid chromatographic method development for anabolic androgenic steroids using a monolithic column Application to animal feed samples |
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