Development of effervescence‐assisted switchable polarity solvent homogeneous liquid‐phase microextraction for the determination of permethrin and deltamethrin in water samples prior to gas chromatography–flame ionization detection
An effervescent tablet‐assisted switchable polarity solvent–based homogeneous liquid‐phase microextraction combined with gas chromatography with flame ionization detection has been conducted for the separation, preconcentration, and detection of permethrin and deltamethrin in the river water specime...
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Veröffentlicht in: | Biomedical chromatography 2022-05, Vol.36 (5), p.e5304-n/a |
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description | An effervescent tablet‐assisted switchable polarity solvent–based homogeneous liquid‐phase microextraction combined with gas chromatography with flame ionization detection has been conducted for the separation, preconcentration, and detection of permethrin and deltamethrin in the river water specimens. Triethylamine (TEA) was utilized as the switchable polarity solvent in this method. The switching process was carried out by the dissolution of an effervescent tablet including an effervescency agent (sodium carbonate) and a proton donor agent (citric acid). Changing the pH of the specimen solution enhanced the conversion of TEA into protonated triethylamine carbonate through the tablet that generated carbon dioxide bubbles in situ. Finally, the addition of sodium hydroxide changed the ionization state of TEA and separated the two phases. Influential factors in the extraction were investigated. According to optimal situations, the limit of detection and the limit of quantification were 0.16 and 0.5 μg L−1 for permethrin and 0.03 and 0.1 μg L−1 for deltamethrin, respectively. The preconcentration factor was 194 in river water samples and inter‐ and intra‐day precision (relative standard deviation %; n = 5) was |
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Triethylamine (TEA) was utilized as the switchable polarity solvent in this method. The switching process was carried out by the dissolution of an effervescent tablet including an effervescency agent (sodium carbonate) and a proton donor agent (citric acid). Changing the pH of the specimen solution enhanced the conversion of TEA into protonated triethylamine carbonate through the tablet that generated carbon dioxide bubbles in situ. Finally, the addition of sodium hydroxide changed the ionization state of TEA and separated the two phases. Influential factors in the extraction were investigated. According to optimal situations, the limit of detection and the limit of quantification were 0.16 and 0.5 μg L−1 for permethrin and 0.03 and 0.1 μg L−1 for deltamethrin, respectively. The preconcentration factor was 194 in river water samples and inter‐ and intra‐day precision (relative standard deviation %; n = 5) was <5%. The extraction recovery was obtained in the range of 93.0%–97% for permethrin and deltamethrin in water samples.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.5304</identifier><identifier>PMID: 34964146</identifier><language>eng</language><publisher>England</publisher><subject>Chromatography, Gas ; effervescent tablet ; Flame Ionization ; homogeneous liquid–liquid microextraction ; Limit of Detection ; Liquid Phase Microextraction - methods ; Nitriles ; Permethrin ; permethrin and deltamethrin ; Pyrethrins ; Solvents - chemistry ; switchable polarity solvent ; Tablets ; Water ; water samples</subject><ispartof>Biomedical chromatography, 2022-05, Vol.36 (5), p.e5304-n/a</ispartof><rights>2021 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3214-c34b80504829aa954cc46f2d0f511d0968247f606ed0de6394f26bbd4d87bdf73</citedby><cites>FETCH-LOGICAL-c3214-c34b80504829aa954cc46f2d0f511d0968247f606ed0de6394f26bbd4d87bdf73</cites><orcidid>0000-0003-2836-2575 ; 0000-0002-9328-1408</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbmc.5304$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.5304$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34964146$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Asadi, Tayebeh</creatorcontrib><creatorcontrib>Rahimi Kakavandi, Nader</creatorcontrib><creatorcontrib>Nili Ahmadabadi, Amir</creatorcontrib><creatorcontrib>Heshmati, Ali</creatorcontrib><creatorcontrib>Ranjbar, Akram</creatorcontrib><creatorcontrib>Abdi, Khosrou</creatorcontrib><creatorcontrib>Ezoddin, Maryam</creatorcontrib><title>Development of effervescence‐assisted switchable polarity solvent homogeneous liquid‐phase microextraction for the determination of permethrin and deltamethrin in water samples prior to gas chromatography–flame ionization detection</title><title>Biomedical chromatography</title><addtitle>Biomed Chromatogr</addtitle><description>An effervescent tablet‐assisted switchable polarity solvent–based homogeneous liquid‐phase microextraction combined with gas chromatography with flame ionization detection has been conducted for the separation, preconcentration, and detection of permethrin and deltamethrin in the river water specimens. Triethylamine (TEA) was utilized as the switchable polarity solvent in this method. The switching process was carried out by the dissolution of an effervescent tablet including an effervescency agent (sodium carbonate) and a proton donor agent (citric acid). Changing the pH of the specimen solution enhanced the conversion of TEA into protonated triethylamine carbonate through the tablet that generated carbon dioxide bubbles in situ. Finally, the addition of sodium hydroxide changed the ionization state of TEA and separated the two phases. Influential factors in the extraction were investigated. According to optimal situations, the limit of detection and the limit of quantification were 0.16 and 0.5 μg L−1 for permethrin and 0.03 and 0.1 μg L−1 for deltamethrin, respectively. The preconcentration factor was 194 in river water samples and inter‐ and intra‐day precision (relative standard deviation %; n = 5) was <5%. The extraction recovery was obtained in the range of 93.0%–97% for permethrin and deltamethrin in water samples.</description><subject>Chromatography, Gas</subject><subject>effervescent tablet</subject><subject>Flame Ionization</subject><subject>homogeneous liquid–liquid microextraction</subject><subject>Limit of Detection</subject><subject>Liquid Phase Microextraction - methods</subject><subject>Nitriles</subject><subject>Permethrin</subject><subject>permethrin and deltamethrin</subject><subject>Pyrethrins</subject><subject>Solvents - chemistry</subject><subject>switchable polarity solvent</subject><subject>Tablets</subject><subject>Water</subject><subject>water samples</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc2OFCEUhStG47SjiU9gWLqpESiKqlpqj3_JGDe6rlBw6cJAUQN0t-1qHsHEN5y97yDVPaMrEwLhcu53wzlF8ZzgC4IxfTU4eVFXmD0oVgR3XYlbTB4WK0x5V1Zt050VT2L8hjHuOG0eF2cV6zgjjK-K35ewA-tnB1NCXiPQGsIOooRJwu3NTxGjiQkUinuT5CgGC2j2VgSTDih6u1v6Ru_8Bibw24isud4alTvnUURAzsjg4XsKQibjJ6R9QGkEpCBBcGYSx2oePOcrpDGYCYlJ5XebxH0hr73IehSFmy1ENAezcDzaiIjkGLwTyW-CmMfD7c0vbXMnylzz44Rfhh3HPy0eaWEjPLs7z4uv795-WX8orz6__7h-fVXKihKWdza0uMaspZ0QXc2kZFxThXVNiMomtpQ1mmMOCivgVcc05cOgmGqbQemmOi9enrhz8NdbiKl3JltqrTia1FNOclwVrdt_0uxTjAF0nz_nRDj0BPdLuH0Ot1_CzdIXd9Tt4ED9Fd6nmQXlSbA3Fg7_BfVvPq2PwD_1Z7nd</recordid><startdate>202205</startdate><enddate>202205</enddate><creator>Asadi, Tayebeh</creator><creator>Rahimi Kakavandi, Nader</creator><creator>Nili Ahmadabadi, Amir</creator><creator>Heshmati, Ali</creator><creator>Ranjbar, Akram</creator><creator>Abdi, Khosrou</creator><creator>Ezoddin, Maryam</creator><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><orcidid>https://orcid.org/0000-0003-2836-2575</orcidid><orcidid>https://orcid.org/0000-0002-9328-1408</orcidid></search><sort><creationdate>202205</creationdate><title>Development of effervescence‐assisted switchable polarity solvent homogeneous liquid‐phase microextraction for the determination of permethrin and deltamethrin in water samples prior to gas chromatography–flame ionization detection</title><author>Asadi, Tayebeh ; Rahimi Kakavandi, Nader ; Nili Ahmadabadi, Amir ; Heshmati, Ali ; Ranjbar, Akram ; Abdi, Khosrou ; Ezoddin, Maryam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3214-c34b80504829aa954cc46f2d0f511d0968247f606ed0de6394f26bbd4d87bdf73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Chromatography, Gas</topic><topic>effervescent tablet</topic><topic>Flame Ionization</topic><topic>homogeneous liquid–liquid microextraction</topic><topic>Limit of Detection</topic><topic>Liquid Phase Microextraction - methods</topic><topic>Nitriles</topic><topic>Permethrin</topic><topic>permethrin and deltamethrin</topic><topic>Pyrethrins</topic><topic>Solvents - chemistry</topic><topic>switchable polarity solvent</topic><topic>Tablets</topic><topic>Water</topic><topic>water samples</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asadi, Tayebeh</creatorcontrib><creatorcontrib>Rahimi Kakavandi, Nader</creatorcontrib><creatorcontrib>Nili Ahmadabadi, Amir</creatorcontrib><creatorcontrib>Heshmati, Ali</creatorcontrib><creatorcontrib>Ranjbar, Akram</creatorcontrib><creatorcontrib>Abdi, Khosrou</creatorcontrib><creatorcontrib>Ezoddin, Maryam</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>Biomedical chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asadi, Tayebeh</au><au>Rahimi Kakavandi, Nader</au><au>Nili Ahmadabadi, Amir</au><au>Heshmati, Ali</au><au>Ranjbar, Akram</au><au>Abdi, Khosrou</au><au>Ezoddin, Maryam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of effervescence‐assisted switchable polarity solvent homogeneous liquid‐phase microextraction for the determination of permethrin and deltamethrin in water samples prior to gas chromatography–flame ionization detection</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed Chromatogr</addtitle><date>2022-05</date><risdate>2022</risdate><volume>36</volume><issue>5</issue><spage>e5304</spage><epage>n/a</epage><pages>e5304-n/a</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>An effervescent tablet‐assisted switchable polarity solvent–based homogeneous liquid‐phase microextraction combined with gas chromatography with flame ionization detection has been conducted for the separation, preconcentration, and detection of permethrin and deltamethrin in the river water specimens. Triethylamine (TEA) was utilized as the switchable polarity solvent in this method. The switching process was carried out by the dissolution of an effervescent tablet including an effervescency agent (sodium carbonate) and a proton donor agent (citric acid). Changing the pH of the specimen solution enhanced the conversion of TEA into protonated triethylamine carbonate through the tablet that generated carbon dioxide bubbles in situ. Finally, the addition of sodium hydroxide changed the ionization state of TEA and separated the two phases. Influential factors in the extraction were investigated. According to optimal situations, the limit of detection and the limit of quantification were 0.16 and 0.5 μg L−1 for permethrin and 0.03 and 0.1 μg L−1 for deltamethrin, respectively. The preconcentration factor was 194 in river water samples and inter‐ and intra‐day precision (relative standard deviation %; n = 5) was <5%. The extraction recovery was obtained in the range of 93.0%–97% for permethrin and deltamethrin in water samples.</abstract><cop>England</cop><pmid>34964146</pmid><doi>10.1002/bmc.5304</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2836-2575</orcidid><orcidid>https://orcid.org/0000-0002-9328-1408</orcidid></addata></record> |
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subjects | Chromatography, Gas effervescent tablet Flame Ionization homogeneous liquid–liquid microextraction Limit of Detection Liquid Phase Microextraction - methods Nitriles Permethrin permethrin and deltamethrin Pyrethrins Solvents - chemistry switchable polarity solvent Tablets Water water samples |
title | Development of effervescence‐assisted switchable polarity solvent homogeneous liquid‐phase microextraction for the determination of permethrin and deltamethrin in water samples prior to gas chromatography–flame ionization detection |
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