Automated method to determine pharmaceutical compounds in wastewater using on-line solid-phase extraction coupled to LC-MS/MS
An automated method was developed using on-line solid-phase extraction (SPE) as a sample preparation step, coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS), for determination of pharmaceutical compounds in wastewater samples at nanograms per liter to micrograms per liter concentr...
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Veröffentlicht in: | Analytical and bioanalytical chemistry 2021-08, Vol.413 (20), p.5147-5160 |
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creator | Marasco Júnior, César Augusto da Silva, Bianca Ferreira Lamarca, Rafaela Silva de Lima Gomes, Paulo Clairmont Feitosa |
description | An automated method was developed using on-line solid-phase extraction (SPE) as a sample preparation step, coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS), for determination of pharmaceutical compounds in wastewater samples at nanograms per liter to micrograms per liter concentration levels. This method is suitable for use in routine analysis, especially in environmental applications, avoiding cross-contamination and requiring minimal sample handling. Results can be obtained rapidly, with a chromatographic run time of only 24 min (including sample preparation and chromatographic analysis). Using a 50 μL injection volume, the method was validated according to international guidelines, considering parameters included in terms of method detection (MDL) and quantification limit (MQL), linearity, inter-day and intra-day precisions, and matrix effects. Assessment of chromatographic efficiency considered peak resolution and asymmetry, and carryover was evaluated to ensure analytical reliability and the ability to reuse the SPE cartridge. The intra- and inter-day precisions were lower than 10 and 17%, respectively. The MDL values ranged from 1×10
-6
to 1 μg L
-1
, while the MQL values were from 0.001 to 3 μg L
-1
. Matrix effects were minimized by isotope dilution calibration. Application of the method to 20 wastewater samples showed that caffeine was the most frequently detected compound, with the highest concentration of 715 μg L
-1
, while other pharmaceutical compounds were detected in fewer samples and at lower concentrations (up to 8.51 μg L
-1
).
Graphical abstract |
doi_str_mv | 10.1007/s00216-021-03481-7 |
format | Article |
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-6
to 1 μg L
-1
, while the MQL values were from 0.001 to 3 μg L
-1
. Matrix effects were minimized by isotope dilution calibration. Application of the method to 20 wastewater samples showed that caffeine was the most frequently detected compound, with the highest concentration of 715 μg L
-1
, while other pharmaceutical compounds were detected in fewer samples and at lower concentrations (up to 8.51 μg L
-1
).
Graphical abstract</description><identifier>ISSN: 1618-2642</identifier><identifier>EISSN: 1618-2650</identifier><identifier>DOI: 10.1007/s00216-021-03481-7</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analysis ; Analytical Chemistry ; Automation ; Biochemistry ; Caffeine ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Chromatography ; Contamination ; Dilution ; Drugs ; Extraction (Chemistry) ; Food Science ; Ions ; Laboratory Medicine ; Liquid chromatography ; Mass spectrometry ; Mass spectroscopy ; Methods ; Monitoring/Environmental Analysis ; Pharmaceuticals ; Reliability analysis ; Research Paper ; Sample preparation ; Solid phases ; Wastewater</subject><ispartof>Analytical and bioanalytical chemistry, 2021-08, Vol.413 (20), p.5147-5160</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>COPYRIGHT 2021 Springer</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-98e899e63cd1067e4cf022a64430542fb3c8e1dc56f66af7aabf281716bc6fa73</citedby><cites>FETCH-LOGICAL-c391t-98e899e63cd1067e4cf022a64430542fb3c8e1dc56f66af7aabf281716bc6fa73</cites><orcidid>0000-0002-5517-6666 ; 0000-0003-0454-3419 ; 0000-0002-4837-6352 ; 0000-0002-8605-8013</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00216-021-03481-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00216-021-03481-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Marasco Júnior, César Augusto</creatorcontrib><creatorcontrib>da Silva, Bianca Ferreira</creatorcontrib><creatorcontrib>Lamarca, Rafaela Silva</creatorcontrib><creatorcontrib>de Lima Gomes, Paulo Clairmont Feitosa</creatorcontrib><title>Automated method to determine pharmaceutical compounds in wastewater using on-line solid-phase extraction coupled to LC-MS/MS</title><title>Analytical and bioanalytical chemistry</title><addtitle>Anal Bioanal Chem</addtitle><description>An automated method was developed using on-line solid-phase extraction (SPE) as a sample preparation step, coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS), for determination of pharmaceutical compounds in wastewater samples at nanograms per liter to micrograms per liter concentration levels. This method is suitable for use in routine analysis, especially in environmental applications, avoiding cross-contamination and requiring minimal sample handling. Results can be obtained rapidly, with a chromatographic run time of only 24 min (including sample preparation and chromatographic analysis). Using a 50 μL injection volume, the method was validated according to international guidelines, considering parameters included in terms of method detection (MDL) and quantification limit (MQL), linearity, inter-day and intra-day precisions, and matrix effects. Assessment of chromatographic efficiency considered peak resolution and asymmetry, and carryover was evaluated to ensure analytical reliability and the ability to reuse the SPE cartridge. The intra- and inter-day precisions were lower than 10 and 17%, respectively. The MDL values ranged from 1×10
-6
to 1 μg L
-1
, while the MQL values were from 0.001 to 3 μg L
-1
. Matrix effects were minimized by isotope dilution calibration. Application of the method to 20 wastewater samples showed that caffeine was the most frequently detected compound, with the highest concentration of 715 μg L
-1
, while other pharmaceutical compounds were detected in fewer samples and at lower concentrations (up to 8.51 μg L
-1
).
Graphical abstract</description><subject>Analysis</subject><subject>Analytical Chemistry</subject><subject>Automation</subject><subject>Biochemistry</subject><subject>Caffeine</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatography</subject><subject>Contamination</subject><subject>Dilution</subject><subject>Drugs</subject><subject>Extraction (Chemistry)</subject><subject>Food Science</subject><subject>Ions</subject><subject>Laboratory Medicine</subject><subject>Liquid chromatography</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Methods</subject><subject>Monitoring/Environmental Analysis</subject><subject>Pharmaceuticals</subject><subject>Reliability analysis</subject><subject>Research Paper</subject><subject>Sample preparation</subject><subject>Solid 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method to determine pharmaceutical compounds in wastewater using on-line solid-phase extraction coupled to LC-MS/MS</title><author>Marasco Júnior, César Augusto ; da Silva, Bianca Ferreira ; Lamarca, Rafaela Silva ; de Lima Gomes, Paulo Clairmont Feitosa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-98e899e63cd1067e4cf022a64430542fb3c8e1dc56f66af7aabf281716bc6fa73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Analysis</topic><topic>Analytical Chemistry</topic><topic>Automation</topic><topic>Biochemistry</topic><topic>Caffeine</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chromatography</topic><topic>Contamination</topic><topic>Dilution</topic><topic>Drugs</topic><topic>Extraction (Chemistry)</topic><topic>Food Science</topic><topic>Ions</topic><topic>Laboratory 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Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical and bioanalytical chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marasco Júnior, César Augusto</au><au>da Silva, Bianca Ferreira</au><au>Lamarca, Rafaela Silva</au><au>de Lima Gomes, Paulo Clairmont Feitosa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Automated method to determine pharmaceutical compounds in wastewater using on-line solid-phase extraction coupled to LC-MS/MS</atitle><jtitle>Analytical and bioanalytical chemistry</jtitle><stitle>Anal Bioanal Chem</stitle><date>2021-08-01</date><risdate>2021</risdate><volume>413</volume><issue>20</issue><spage>5147</spage><epage>5160</epage><pages>5147-5160</pages><issn>1618-2642</issn><eissn>1618-2650</eissn><abstract>An automated method was developed using on-line solid-phase extraction (SPE) as a sample preparation step, coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS), for determination of pharmaceutical compounds in wastewater samples at nanograms per liter to micrograms per liter concentration levels. This method is suitable for use in routine analysis, especially in environmental applications, avoiding cross-contamination and requiring minimal sample handling. Results can be obtained rapidly, with a chromatographic run time of only 24 min (including sample preparation and chromatographic analysis). Using a 50 μL injection volume, the method was validated according to international guidelines, considering parameters included in terms of method detection (MDL) and quantification limit (MQL), linearity, inter-day and intra-day precisions, and matrix effects. Assessment of chromatographic efficiency considered peak resolution and asymmetry, and carryover was evaluated to ensure analytical reliability and the ability to reuse the SPE cartridge. The intra- and inter-day precisions were lower than 10 and 17%, respectively. The MDL values ranged from 1×10
-6
to 1 μg L
-1
, while the MQL values were from 0.001 to 3 μg L
-1
. Matrix effects were minimized by isotope dilution calibration. Application of the method to 20 wastewater samples showed that caffeine was the most frequently detected compound, with the highest concentration of 715 μg L
-1
, while other pharmaceutical compounds were detected in fewer samples and at lower concentrations (up to 8.51 μg L
-1
).
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subjects | Analysis Analytical Chemistry Automation Biochemistry Caffeine Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Chromatography Contamination Dilution Drugs Extraction (Chemistry) Food Science Ions Laboratory Medicine Liquid chromatography Mass spectrometry Mass spectroscopy Methods Monitoring/Environmental Analysis Pharmaceuticals Reliability analysis Research Paper Sample preparation Solid phases Wastewater |
title | Automated method to determine pharmaceutical compounds in wastewater using on-line solid-phase extraction coupled to LC-MS/MS |
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