Quantification of fatty acids in the muscle of Antarctic fish Trematomus bernacchii by gas chromatography-mass spectrometry: Optimization of the analytical methodology
This work presents data on the quantification of fatty acids (FAs, in terms of mass unit per tissue weight) in the muscle of Trematomus bernacchii, a key species in Antarctica, often used as bioindicator for contamination studies. Modifications in fatty acids content should be considered a useful bi...
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description | This work presents data on the quantification of fatty acids (FAs, in terms of mass unit per tissue weight) in the muscle of Trematomus bernacchii, a key species in Antarctica, often used as bioindicator for contamination studies. Modifications in fatty acids content should be considered a useful biomarker to study how contaminants affect Antarctic biota. Until now, very few studies quantified fatty acids of muscle of T. bernacchii, and only as percentage of a single fatty acid on total lipids. To perform the quantification of fatty acids, we used an analytical method based on a fast microwave-assisted extraction of lipids from a lyophilized sample, a base-catalyzed trans-esterification of lipid extract to obtain Fatty Acids Methyl Esters (FAMEs), and a separation and identification of FAMEs by gas chromatography-mass spectrometry. With the optimized and validated method, a fast and accurate separation of Fatty Acids Methyl Esters was performed in 43 min. The linearity was checked up to about 320 μg mL−1; limit of detection and limit of quantification are in the range 4–22 μg mL−1 and 13–66 μg mL−1, respectively. The optimized method showed a good accuracy and precision. Major fatty acids were 14:0, 16:0, 16:1n7, 18:1n9, 18:1n7, 20:1n9, 20:5n3 and 22:6n3. Quantified FAs compute for about 47 mg g−1 tissue dry weight (dw), with 9.1 ± 0.1 mg g−1 dw of saturated FAs, 25.5 ± 0.1 mg g−1 dw of mono-unsaturated FAs, and 12.2 ± 0.1 mg g−1 dw of poly-unsaturated FAs.
•Fatty acids in muscle of Trematomus bernacchii: set-up of the analytical methodology.•Accurate Microwave-assisted extraction of lipids preceded by lyophilization.•LOD and LOQ: from ∼4 to ∼22 μg/mL, and from ∼13 to ∼66 μg/mL, respectively.•Good accuracy (recovery test ∼96%) and precision (intra-day ≤4%, inter-day ≤7%).•Quantified FAs compute 9.1, 25.5, 12.2 mg g−1 dw for SFA, MUFA, PUFA, respectively. |
doi_str_mv | 10.1016/j.chemosphere.2016.12.140 |
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•Fatty acids in muscle of Trematomus bernacchii: set-up of the analytical methodology.•Accurate Microwave-assisted extraction of lipids preceded by lyophilization.•LOD and LOQ: from ∼4 to ∼22 μg/mL, and from ∼13 to ∼66 μg/mL, respectively.•Good accuracy (recovery test ∼96%) and precision (intra-day ≤4%, inter-day ≤7%).•Quantified FAs compute 9.1, 25.5, 12.2 mg g−1 dw for SFA, MUFA, PUFA, respectively.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2016.12.140</identifier><identifier>PMID: 28107709</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Antarctic Regions ; Esterification ; Fatty Acids - analysis ; Fatty Acids - chemistry ; Fatty acids quantification ; Gas chromatography-mass spectrometry ; Gas Chromatography-Mass Spectrometry - methods ; Lipid profile ; Microwave-assisted extraction ; Muscle ; Muscles - metabolism ; Perciformes - growth & development ; Perciformes - metabolism ; Trematomus bernacchii</subject><ispartof>Chemosphere (Oxford), 2017-04, Vol.173, p.116-123</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-bb6b2b39cd2db9d4d62eec459aaccec96ba739972c802b1418d02aa60b5daf783</citedby><cites>FETCH-LOGICAL-c377t-bb6b2b39cd2db9d4d62eec459aaccec96ba739972c802b1418d02aa60b5daf783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.chemosphere.2016.12.140$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27913,27914,45984</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28107709$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Truzzi, C.</creatorcontrib><creatorcontrib>Illuminati, S.</creatorcontrib><creatorcontrib>Annibaldi, A.</creatorcontrib><creatorcontrib>Antonucci, M.</creatorcontrib><creatorcontrib>Scarponi, G.</creatorcontrib><title>Quantification of fatty acids in the muscle of Antarctic fish Trematomus bernacchii by gas chromatography-mass spectrometry: Optimization of the analytical methodology</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>This work presents data on the quantification of fatty acids (FAs, in terms of mass unit per tissue weight) in the muscle of Trematomus bernacchii, a key species in Antarctica, often used as bioindicator for contamination studies. Modifications in fatty acids content should be considered a useful biomarker to study how contaminants affect Antarctic biota. Until now, very few studies quantified fatty acids of muscle of T. bernacchii, and only as percentage of a single fatty acid on total lipids. To perform the quantification of fatty acids, we used an analytical method based on a fast microwave-assisted extraction of lipids from a lyophilized sample, a base-catalyzed trans-esterification of lipid extract to obtain Fatty Acids Methyl Esters (FAMEs), and a separation and identification of FAMEs by gas chromatography-mass spectrometry. With the optimized and validated method, a fast and accurate separation of Fatty Acids Methyl Esters was performed in 43 min. The linearity was checked up to about 320 μg mL−1; limit of detection and limit of quantification are in the range 4–22 μg mL−1 and 13–66 μg mL−1, respectively. The optimized method showed a good accuracy and precision. Major fatty acids were 14:0, 16:0, 16:1n7, 18:1n9, 18:1n7, 20:1n9, 20:5n3 and 22:6n3. Quantified FAs compute for about 47 mg g−1 tissue dry weight (dw), with 9.1 ± 0.1 mg g−1 dw of saturated FAs, 25.5 ± 0.1 mg g−1 dw of mono-unsaturated FAs, and 12.2 ± 0.1 mg g−1 dw of poly-unsaturated FAs.
•Fatty acids in muscle of Trematomus bernacchii: set-up of the analytical methodology.•Accurate Microwave-assisted extraction of lipids preceded by lyophilization.•LOD and LOQ: from ∼4 to ∼22 μg/mL, and from ∼13 to ∼66 μg/mL, respectively.•Good accuracy (recovery test ∼96%) and precision (intra-day ≤4%, inter-day ≤7%).•Quantified FAs compute 9.1, 25.5, 12.2 mg g−1 dw for SFA, MUFA, PUFA, respectively.</description><subject>Animals</subject><subject>Antarctic Regions</subject><subject>Esterification</subject><subject>Fatty Acids - analysis</subject><subject>Fatty Acids - chemistry</subject><subject>Fatty acids quantification</subject><subject>Gas chromatography-mass spectrometry</subject><subject>Gas Chromatography-Mass Spectrometry - methods</subject><subject>Lipid profile</subject><subject>Microwave-assisted extraction</subject><subject>Muscle</subject><subject>Muscles - metabolism</subject><subject>Perciformes - growth & development</subject><subject>Perciformes - metabolism</subject><subject>Trematomus bernacchii</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1TAQhSMEopfCKyCzY5NgO79mV12VH6lShVTW1tie3PgqiYPtIIUX4jVxdEvFktVIc76ZM_bJsneMFoyy5sO50ANOLiwDeix4ahWMF6yiz7ID61qRMy6659mB0qrOm7qsr7JXIZwpTWQtXmZXvGO0bak4ZL-_rTBH21sN0bqZuJ70EONGQFsTiJ1JHJBMa9Aj7uLNHMHraDXpbRjIg8cJoks6Uehn0HqwlqiNnCAQPXi3qycPy7DlE4RAwoI6pjZGv30k90u0k_31ZL17wQzjlgxgJIkanHGjO22vsxc9jAHfPNbr7Pun24fjl_zu_vPX481drsu2jblSjeKqFNpwo4SpTMMRdVULSKehFo2CthSi5bqjXLGKdYZygIaq2kDfduV19v6yd_Hux4ohyskGjeMIM7o1SNY1rO7ajlcJFRdUexeCx14u3k7gN8mo3HOSZ_lPTnLPSTIuU05p9u2jzaomNE-Tf4NJwPECYHrsT4teBm1x1misTz8ojbP_YfMH2v6wZw</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Truzzi, C.</creator><creator>Illuminati, S.</creator><creator>Annibaldi, A.</creator><creator>Antonucci, M.</creator><creator>Scarponi, G.</creator><general>Elsevier Ltd</general><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>7X8</scope></search><sort><creationdate>20170401</creationdate><title>Quantification of fatty acids in the muscle of Antarctic fish Trematomus bernacchii by gas chromatography-mass spectrometry: Optimization of the analytical methodology</title><author>Truzzi, C. ; Illuminati, S. ; Annibaldi, A. ; Antonucci, M. ; Scarponi, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-bb6b2b39cd2db9d4d62eec459aaccec96ba739972c802b1418d02aa60b5daf783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Antarctic Regions</topic><topic>Esterification</topic><topic>Fatty Acids - analysis</topic><topic>Fatty Acids - chemistry</topic><topic>Fatty acids quantification</topic><topic>Gas chromatography-mass spectrometry</topic><topic>Gas Chromatography-Mass Spectrometry - methods</topic><topic>Lipid profile</topic><topic>Microwave-assisted extraction</topic><topic>Muscle</topic><topic>Muscles - metabolism</topic><topic>Perciformes - growth & development</topic><topic>Perciformes - metabolism</topic><topic>Trematomus bernacchii</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Truzzi, C.</creatorcontrib><creatorcontrib>Illuminati, S.</creatorcontrib><creatorcontrib>Annibaldi, A.</creatorcontrib><creatorcontrib>Antonucci, M.</creatorcontrib><creatorcontrib>Scarponi, G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Truzzi, C.</au><au>Illuminati, S.</au><au>Annibaldi, A.</au><au>Antonucci, M.</au><au>Scarponi, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of fatty acids in the muscle of Antarctic fish Trematomus bernacchii by gas chromatography-mass spectrometry: Optimization of the analytical methodology</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2017-04-01</date><risdate>2017</risdate><volume>173</volume><spage>116</spage><epage>123</epage><pages>116-123</pages><issn>0045-6535</issn><eissn>1879-1298</eissn><abstract>This work presents data on the quantification of fatty acids (FAs, in terms of mass unit per tissue weight) in the muscle of Trematomus bernacchii, a key species in Antarctica, often used as bioindicator for contamination studies. Modifications in fatty acids content should be considered a useful biomarker to study how contaminants affect Antarctic biota. Until now, very few studies quantified fatty acids of muscle of T. bernacchii, and only as percentage of a single fatty acid on total lipids. To perform the quantification of fatty acids, we used an analytical method based on a fast microwave-assisted extraction of lipids from a lyophilized sample, a base-catalyzed trans-esterification of lipid extract to obtain Fatty Acids Methyl Esters (FAMEs), and a separation and identification of FAMEs by gas chromatography-mass spectrometry. With the optimized and validated method, a fast and accurate separation of Fatty Acids Methyl Esters was performed in 43 min. The linearity was checked up to about 320 μg mL−1; limit of detection and limit of quantification are in the range 4–22 μg mL−1 and 13–66 μg mL−1, respectively. The optimized method showed a good accuracy and precision. Major fatty acids were 14:0, 16:0, 16:1n7, 18:1n9, 18:1n7, 20:1n9, 20:5n3 and 22:6n3. Quantified FAs compute for about 47 mg g−1 tissue dry weight (dw), with 9.1 ± 0.1 mg g−1 dw of saturated FAs, 25.5 ± 0.1 mg g−1 dw of mono-unsaturated FAs, and 12.2 ± 0.1 mg g−1 dw of poly-unsaturated FAs.
•Fatty acids in muscle of Trematomus bernacchii: set-up of the analytical methodology.•Accurate Microwave-assisted extraction of lipids preceded by lyophilization.•LOD and LOQ: from ∼4 to ∼22 μg/mL, and from ∼13 to ∼66 μg/mL, respectively.•Good accuracy (recovery test ∼96%) and precision (intra-day ≤4%, inter-day ≤7%).•Quantified FAs compute 9.1, 25.5, 12.2 mg g−1 dw for SFA, MUFA, PUFA, respectively.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28107709</pmid><doi>10.1016/j.chemosphere.2016.12.140</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Antarctic Regions Esterification Fatty Acids - analysis Fatty Acids - chemistry Fatty acids quantification Gas chromatography-mass spectrometry Gas Chromatography-Mass Spectrometry - methods Lipid profile Microwave-assisted extraction Muscle Muscles - metabolism Perciformes - growth & development Perciformes - metabolism Trematomus bernacchii |
title | Quantification of fatty acids in the muscle of Antarctic fish Trematomus bernacchii by gas chromatography-mass spectrometry: Optimization of the analytical methodology |
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