Application of molecularly imprinted polymer solid-phase extraction for salivary cotinine
A method constituted by molecularly imprinted solid-phase extraction (MISPE) with high-performance liquid chromatography coupled to diode array detector (HPLC-DAD) was developed for cotinine analysis in saliva samples. For this purpose, the separation was carried out with a C18 reversed-phase column...
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Veröffentlicht in: | Analytical and bioanalytical chemistry 2011-06, Vol.400 (7), p.2109 |
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description | A method constituted by molecularly imprinted solid-phase extraction (MISPE) with high-performance liquid chromatography coupled to diode array detector (HPLC-DAD) was developed for cotinine analysis in saliva samples. For this purpose, the separation was carried out with a C18 reversed-phase column at 20 °C. The mobile phase which was composed of a mixture of 09:91 (v/v) acetonitrile/phosphate buffer, pH 6.3, was delivered with isocratic flow rate at 1.4 mL min [.sup.1]. Employing MISPE, the best conditions were achieved with 1.5 mL of saliva plus 1.5 mL of 0.1 mol L [.sup.1] of acetate buffer, pH 5.5, which were then passed through a cartridge previously conditioned with 2 mL acetonitrile, 2 mL methanol, and 2 mL of 0.1 mol L [.sup.1] sodium acetate buffer, pH 5.5. The washing was carried out with 1 mL deionized water, 1 mL of 0.1 mol L [.sup.1] sodium hydroxide, and 1 mL hexane; finally; the cotinine elution was carried out with 3 mL methanol/water (97.5: 2.5, v/v). Linearity ranged from 30 to 500 ng mL [.sup.1] with r>0.99. Intra-assay, interassay precision, and accuracy ranged from 3.1% to 10.1%, 5.2% to 15.9%, and 99.22% to 111.17%, respectively. The detection and quantification limits were 10 and 30 ng mL [.sup.1], respectively. This investigation has provided a reliable method for routine cotinine determination in saliva, and it is an important tool for monitoring cigarette smoke exposure in smokers. The method was applied in five smokers' samples who consumed around five to 20 cigarettes per day and the values of cotinine in saliva were from 66.7 to 316.16 ng mL [.sup.1]. Keywords Molecularly imprinted polymer. Solid-phase extraction * Cotinine * Saliva * Liquid chromatography |
doi_str_mv | 10.1007/00216-1311-4870-1 |
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For this purpose, the separation was carried out with a C18 reversed-phase column at 20 °C. The mobile phase which was composed of a mixture of 09:91 (v/v) acetonitrile/phosphate buffer, pH 6.3, was delivered with isocratic flow rate at 1.4 mL min [.sup.1]. Employing MISPE, the best conditions were achieved with 1.5 mL of saliva plus 1.5 mL of 0.1 mol L [.sup.1] of acetate buffer, pH 5.5, which were then passed through a cartridge previously conditioned with 2 mL acetonitrile, 2 mL methanol, and 2 mL of 0.1 mol L [.sup.1] sodium acetate buffer, pH 5.5. The washing was carried out with 1 mL deionized water, 1 mL of 0.1 mol L [.sup.1] sodium hydroxide, and 1 mL hexane; finally; the cotinine elution was carried out with 3 mL methanol/water (97.5: 2.5, v/v). Linearity ranged from 30 to 500 ng mL [.sup.1] with r>0.99. Intra-assay, interassay precision, and accuracy ranged from 3.1% to 10.1%, 5.2% to 15.9%, and 99.22% to 111.17%, respectively. The detection and quantification limits were 10 and 30 ng mL [.sup.1], respectively. This investigation has provided a reliable method for routine cotinine determination in saliva, and it is an important tool for monitoring cigarette smoke exposure in smokers. The method was applied in five smokers' samples who consumed around five to 20 cigarettes per day and the values of cotinine in saliva were from 66.7 to 316.16 ng mL [.sup.1]. Keywords Molecularly imprinted polymer. Solid-phase extraction * Cotinine * Saliva * Liquid chromatography</description><identifier>ISSN: 1618-2642</identifier><identifier>DOI: 10.1007/00216-1311-4870-1</identifier><language>eng</language><publisher>Springer</publisher><subject>Cotinine ; Detectors ; High performance liquid chromatography ; Hydroxides ; Nitriles ; Polymer industry ; Polymers ; Smoking</subject><ispartof>Analytical and bioanalytical chemistry, 2011-06, Vol.400 (7), p.2109</ispartof><rights>COPYRIGHT 2011 Springer</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></links><search><creatorcontrib>Vitor, Ricardo Vilela</creatorcontrib><creatorcontrib>Goncalves Ma</creatorcontrib><creatorcontrib>Figueiredo, Eduardo Costa</creatorcontrib><creatorcontrib>Ma</creatorcontrib><title>Application of molecularly imprinted polymer solid-phase extraction for salivary cotinine</title><title>Analytical and bioanalytical chemistry</title><description>A method constituted by molecularly imprinted solid-phase extraction (MISPE) with high-performance liquid chromatography coupled to diode array detector (HPLC-DAD) was developed for cotinine analysis in saliva samples. For this purpose, the separation was carried out with a C18 reversed-phase column at 20 °C. The mobile phase which was composed of a mixture of 09:91 (v/v) acetonitrile/phosphate buffer, pH 6.3, was delivered with isocratic flow rate at 1.4 mL min [.sup.1]. Employing MISPE, the best conditions were achieved with 1.5 mL of saliva plus 1.5 mL of 0.1 mol L [.sup.1] of acetate buffer, pH 5.5, which were then passed through a cartridge previously conditioned with 2 mL acetonitrile, 2 mL methanol, and 2 mL of 0.1 mol L [.sup.1] sodium acetate buffer, pH 5.5. The washing was carried out with 1 mL deionized water, 1 mL of 0.1 mol L [.sup.1] sodium hydroxide, and 1 mL hexane; finally; the cotinine elution was carried out with 3 mL methanol/water (97.5: 2.5, v/v). Linearity ranged from 30 to 500 ng mL [.sup.1] with r>0.99. Intra-assay, interassay precision, and accuracy ranged from 3.1% to 10.1%, 5.2% to 15.9%, and 99.22% to 111.17%, respectively. The detection and quantification limits were 10 and 30 ng mL [.sup.1], respectively. This investigation has provided a reliable method for routine cotinine determination in saliva, and it is an important tool for monitoring cigarette smoke exposure in smokers. The method was applied in five smokers' samples who consumed around five to 20 cigarettes per day and the values of cotinine in saliva were from 66.7 to 316.16 ng mL [.sup.1]. Keywords Molecularly imprinted polymer. Solid-phase extraction * Cotinine * Saliva * Liquid chromatography</description><subject>Cotinine</subject><subject>Detectors</subject><subject>High performance liquid chromatography</subject><subject>Hydroxides</subject><subject>Nitriles</subject><subject>Polymer industry</subject><subject>Polymers</subject><subject>Smoking</subject><issn>1618-2642</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptTrtOwzAU9QASpfABbJaYXe51_GjGquJRqRJLF6bK2NfFyImjJCD694THwIDOcKTz0mHsCmGBAPYGQKIRWCEKtbQg8ITN0OBSSKPkGTsfhlcA1Es0M_a06rqcvBtTaXmJvCmZ_Ft2fT7y1HR9akcKvCv52FDPh5JTEN2LG4jTx9g7_92LZbJcTu-uP3JfxtSmli7YaXR5oMtfnrPd3e1u_SC2j_eb9WorDsZWQltdKVLOKYm1CQE8-CAJYXrnNFG0zzL46AOgsgEgal_XdTReo_WGdDVn1z-zB5dpn9pYvm41afD7VVVrJaE21ZRa_JOaEKhJvrQU06T_KXwCAepjUQ</recordid><startdate>20110615</startdate><enddate>20110615</enddate><creator>Vitor, Ricardo Vilela</creator><creator>Goncalves Ma</creator><creator>Figueiredo, Eduardo Costa</creator><creator>Ma</creator><general>Springer</general><scope/></search><sort><creationdate>20110615</creationdate><title>Application of molecularly imprinted polymer solid-phase extraction for salivary cotinine</title><author>Vitor, Ricardo Vilela ; Goncalves Ma ; Figueiredo, Eduardo Costa ; Ma</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g673-57534e4aa42196dd0c0cd2e10816a5eef7b2dcfcd0147d00f5c999f6c517c6e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Cotinine</topic><topic>Detectors</topic><topic>High performance liquid chromatography</topic><topic>Hydroxides</topic><topic>Nitriles</topic><topic>Polymer industry</topic><topic>Polymers</topic><topic>Smoking</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vitor, Ricardo Vilela</creatorcontrib><creatorcontrib>Goncalves Ma</creatorcontrib><creatorcontrib>Figueiredo, Eduardo Costa</creatorcontrib><creatorcontrib>Ma</creatorcontrib><jtitle>Analytical and bioanalytical chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vitor, Ricardo Vilela</au><au>Goncalves Ma</au><au>Figueiredo, Eduardo Costa</au><au>Ma</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of molecularly imprinted polymer solid-phase extraction for salivary cotinine</atitle><jtitle>Analytical and bioanalytical chemistry</jtitle><date>2011-06-15</date><risdate>2011</risdate><volume>400</volume><issue>7</issue><spage>2109</spage><pages>2109-</pages><issn>1618-2642</issn><abstract>A method constituted by molecularly imprinted solid-phase extraction (MISPE) with high-performance liquid chromatography coupled to diode array detector (HPLC-DAD) was developed for cotinine analysis in saliva samples. For this purpose, the separation was carried out with a C18 reversed-phase column at 20 °C. The mobile phase which was composed of a mixture of 09:91 (v/v) acetonitrile/phosphate buffer, pH 6.3, was delivered with isocratic flow rate at 1.4 mL min [.sup.1]. Employing MISPE, the best conditions were achieved with 1.5 mL of saliva plus 1.5 mL of 0.1 mol L [.sup.1] of acetate buffer, pH 5.5, which were then passed through a cartridge previously conditioned with 2 mL acetonitrile, 2 mL methanol, and 2 mL of 0.1 mol L [.sup.1] sodium acetate buffer, pH 5.5. The washing was carried out with 1 mL deionized water, 1 mL of 0.1 mol L [.sup.1] sodium hydroxide, and 1 mL hexane; finally; the cotinine elution was carried out with 3 mL methanol/water (97.5: 2.5, v/v). Linearity ranged from 30 to 500 ng mL [.sup.1] with r>0.99. Intra-assay, interassay precision, and accuracy ranged from 3.1% to 10.1%, 5.2% to 15.9%, and 99.22% to 111.17%, respectively. The detection and quantification limits were 10 and 30 ng mL [.sup.1], respectively. This investigation has provided a reliable method for routine cotinine determination in saliva, and it is an important tool for monitoring cigarette smoke exposure in smokers. The method was applied in five smokers' samples who consumed around five to 20 cigarettes per day and the values of cotinine in saliva were from 66.7 to 316.16 ng mL [.sup.1]. Keywords Molecularly imprinted polymer. Solid-phase extraction * Cotinine * Saliva * Liquid chromatography</abstract><pub>Springer</pub><doi>10.1007/00216-1311-4870-1</doi></addata></record> |
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subjects | Cotinine Detectors High performance liquid chromatography Hydroxides Nitriles Polymer industry Polymers Smoking |
title | Application of molecularly imprinted polymer solid-phase extraction for salivary cotinine |
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