Liquid chromatography with micelles in open-tube capillaries
The greening efforts in analytical chromatography are mostly on the reduction of chemical waste and the replacement of organic solvents used in the mobile phase. Here, we present a new green liquid chromatography approach in open-tubes with the following advantages and/or features: up to zero chemic...
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description | The greening efforts in analytical chromatography are mostly on the reduction of chemical waste and the replacement of organic solvents used in the mobile phase. Here, we present a new green liquid chromatography approach in open-tubes with the following advantages and/or features: up to zero chemical waste, minimal use of reagents and samples, no preparation of a solid stationary phase, relatively fast separations and reproducible results. The approach was based on the molecular organisation of common long chain ionic surfactants (
i.e.
, hexadecyltrimethylammonium bromide and sodium dodecyl sulfate) to form micelles in solution and at the solid surface-liquid interface. The differential solubilisation or distribution of solutes into these micelles produced the unexpected separation or retention of various types of molecules including aromatic hydrocarbons, anionic, cationic and amphiphilic drugs, pesticides, peptides and a small protein. Chromatography was done in 25-200 μm range inner diameter and 60 or 120 cm long fused silica capillaries against a flow of predominantly aqueous surfactant solutions above the critical micelle concentration as mobile phase. Distribution between these micelles was affected by the mobile phase conditions such as surfactant concentration, pH, salt concentration and organic solvent content used, which we harnessed to demonstrate sample enrichment. Analytical performance was assessed in the separation of pesticides and antioxidants and in real sample matrices. A comparison with reversed phase chromatography for the analysis of a drug combination was also done. This important fundamental behavior of surfactant micelles presented might find use in the development of green extraction technologies, nano-micro separations and portable devices.
Open-tubular liquid chromatography with interfacial micelles. |
doi_str_mv | 10.1039/c8gc00409a |
format | Article |
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i.e.
, hexadecyltrimethylammonium bromide and sodium dodecyl sulfate) to form micelles in solution and at the solid surface-liquid interface. The differential solubilisation or distribution of solutes into these micelles produced the unexpected separation or retention of various types of molecules including aromatic hydrocarbons, anionic, cationic and amphiphilic drugs, pesticides, peptides and a small protein. Chromatography was done in 25-200 μm range inner diameter and 60 or 120 cm long fused silica capillaries against a flow of predominantly aqueous surfactant solutions above the critical micelle concentration as mobile phase. Distribution between these micelles was affected by the mobile phase conditions such as surfactant concentration, pH, salt concentration and organic solvent content used, which we harnessed to demonstrate sample enrichment. Analytical performance was assessed in the separation of pesticides and antioxidants and in real sample matrices. A comparison with reversed phase chromatography for the analysis of a drug combination was also done. This important fundamental behavior of surfactant micelles presented might find use in the development of green extraction technologies, nano-micro separations and portable devices.
Open-tubular liquid chromatography with interfacial micelles.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c8gc00409a</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Antioxidants ; Aromatic hydrocarbons ; Capillaries ; Cetyltrimethylammonium bromide ; Chromatography ; Fused silica ; Green chemistry ; Greening ; Hydrocarbons ; Liquid chromatography ; Micelles ; Molecular chains ; Organic chemistry ; Organic solvents ; Peptides ; Pesticides ; Pollutants ; Portable equipment ; Proteins ; Reagents ; Separation ; Silica ; Silicon dioxide ; Sodium ; Sodium dodecyl sulfate ; Sodium lauryl sulfate ; Solutes ; Stationary phase ; Surfactants ; Sustainable development ; Tubes</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2018, Vol.2 (11), p.2486-2493</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c318t-88c66d6523c1970340d34f4b18f1fe58d65316c1a46cfb3bfc89e831359ea69b3</citedby><cites>FETCH-LOGICAL-c318t-88c66d6523c1970340d34f4b18f1fe58d65316c1a46cfb3bfc89e831359ea69b3</cites><orcidid>0000-0002-8275-9672</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4023,27922,27923,27924</link.rule.ids></links><search><creatorcontrib>Quirino, Joselito P</creatorcontrib><creatorcontrib>Tarongoy, Faustino M</creatorcontrib><title>Liquid chromatography with micelles in open-tube capillaries</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>The greening efforts in analytical chromatography are mostly on the reduction of chemical waste and the replacement of organic solvents used in the mobile phase. Here, we present a new green liquid chromatography approach in open-tubes with the following advantages and/or features: up to zero chemical waste, minimal use of reagents and samples, no preparation of a solid stationary phase, relatively fast separations and reproducible results. The approach was based on the molecular organisation of common long chain ionic surfactants (
i.e.
, hexadecyltrimethylammonium bromide and sodium dodecyl sulfate) to form micelles in solution and at the solid surface-liquid interface. The differential solubilisation or distribution of solutes into these micelles produced the unexpected separation or retention of various types of molecules including aromatic hydrocarbons, anionic, cationic and amphiphilic drugs, pesticides, peptides and a small protein. Chromatography was done in 25-200 μm range inner diameter and 60 or 120 cm long fused silica capillaries against a flow of predominantly aqueous surfactant solutions above the critical micelle concentration as mobile phase. Distribution between these micelles was affected by the mobile phase conditions such as surfactant concentration, pH, salt concentration and organic solvent content used, which we harnessed to demonstrate sample enrichment. Analytical performance was assessed in the separation of pesticides and antioxidants and in real sample matrices. A comparison with reversed phase chromatography for the analysis of a drug combination was also done. This important fundamental behavior of surfactant micelles presented might find use in the development of green extraction technologies, nano-micro separations and portable devices.
Open-tubular liquid chromatography with interfacial micelles.</description><subject>Antioxidants</subject><subject>Aromatic hydrocarbons</subject><subject>Capillaries</subject><subject>Cetyltrimethylammonium bromide</subject><subject>Chromatography</subject><subject>Fused silica</subject><subject>Green chemistry</subject><subject>Greening</subject><subject>Hydrocarbons</subject><subject>Liquid chromatography</subject><subject>Micelles</subject><subject>Molecular chains</subject><subject>Organic chemistry</subject><subject>Organic solvents</subject><subject>Peptides</subject><subject>Pesticides</subject><subject>Pollutants</subject><subject>Portable equipment</subject><subject>Proteins</subject><subject>Reagents</subject><subject>Separation</subject><subject>Silica</subject><subject>Silicon dioxide</subject><subject>Sodium</subject><subject>Sodium dodecyl sulfate</subject><subject>Sodium lauryl sulfate</subject><subject>Solutes</subject><subject>Stationary phase</subject><subject>Surfactants</subject><subject>Sustainable development</subject><subject>Tubes</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpFkMFLwzAUxoMoOKcX70LBm1DNa9I0AS-jzCkUvOi5pK_JltGtXdIi---tVubpffB-fB_8CLkF-giUqSeUa6SUU6XPyAy4YLFKMnp-yiK5JFchbCkFyASfkefCHQZXR7jx7U737drrbnOMvly_iXYOTdOYELl91HZmH_dDZSLUnWsa7Z0J1-TC6iaYm787J58vy4_8NS7eV2_5ooiRgexjKVGIWqQJQ1AZZZzWjFtegbRgTSrHFwOBoLlAW7HKolRGMmCpMlqois3J_dTb-fYwmNCX23bw-3GyTChXqUwypUbqYaLQtyF4Y8vOu532xxJo-WOnzOUq_7WzGOG7CfYBT9y_PfYNontgXg</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Quirino, Joselito P</creator><creator>Tarongoy, Faustino M</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7ST</scope><scope>7U6</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0002-8275-9672</orcidid></search><sort><creationdate>2018</creationdate><title>Liquid chromatography with micelles in open-tube capillaries</title><author>Quirino, Joselito P ; Tarongoy, Faustino M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c318t-88c66d6523c1970340d34f4b18f1fe58d65316c1a46cfb3bfc89e831359ea69b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antioxidants</topic><topic>Aromatic hydrocarbons</topic><topic>Capillaries</topic><topic>Cetyltrimethylammonium bromide</topic><topic>Chromatography</topic><topic>Fused silica</topic><topic>Green chemistry</topic><topic>Greening</topic><topic>Hydrocarbons</topic><topic>Liquid chromatography</topic><topic>Micelles</topic><topic>Molecular chains</topic><topic>Organic chemistry</topic><topic>Organic solvents</topic><topic>Peptides</topic><topic>Pesticides</topic><topic>Pollutants</topic><topic>Portable equipment</topic><topic>Proteins</topic><topic>Reagents</topic><topic>Separation</topic><topic>Silica</topic><topic>Silicon dioxide</topic><topic>Sodium</topic><topic>Sodium dodecyl sulfate</topic><topic>Sodium lauryl sulfate</topic><topic>Solutes</topic><topic>Stationary phase</topic><topic>Surfactants</topic><topic>Sustainable development</topic><topic>Tubes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quirino, Joselito P</creatorcontrib><creatorcontrib>Tarongoy, Faustino M</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quirino, Joselito P</au><au>Tarongoy, Faustino M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liquid chromatography with micelles in open-tube capillaries</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2018</date><risdate>2018</risdate><volume>2</volume><issue>11</issue><spage>2486</spage><epage>2493</epage><pages>2486-2493</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>The greening efforts in analytical chromatography are mostly on the reduction of chemical waste and the replacement of organic solvents used in the mobile phase. Here, we present a new green liquid chromatography approach in open-tubes with the following advantages and/or features: up to zero chemical waste, minimal use of reagents and samples, no preparation of a solid stationary phase, relatively fast separations and reproducible results. The approach was based on the molecular organisation of common long chain ionic surfactants (
i.e.
, hexadecyltrimethylammonium bromide and sodium dodecyl sulfate) to form micelles in solution and at the solid surface-liquid interface. The differential solubilisation or distribution of solutes into these micelles produced the unexpected separation or retention of various types of molecules including aromatic hydrocarbons, anionic, cationic and amphiphilic drugs, pesticides, peptides and a small protein. Chromatography was done in 25-200 μm range inner diameter and 60 or 120 cm long fused silica capillaries against a flow of predominantly aqueous surfactant solutions above the critical micelle concentration as mobile phase. Distribution between these micelles was affected by the mobile phase conditions such as surfactant concentration, pH, salt concentration and organic solvent content used, which we harnessed to demonstrate sample enrichment. Analytical performance was assessed in the separation of pesticides and antioxidants and in real sample matrices. A comparison with reversed phase chromatography for the analysis of a drug combination was also done. This important fundamental behavior of surfactant micelles presented might find use in the development of green extraction technologies, nano-micro separations and portable devices.
Open-tubular liquid chromatography with interfacial micelles.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c8gc00409a</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8275-9672</orcidid></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Antioxidants Aromatic hydrocarbons Capillaries Cetyltrimethylammonium bromide Chromatography Fused silica Green chemistry Greening Hydrocarbons Liquid chromatography Micelles Molecular chains Organic chemistry Organic solvents Peptides Pesticides Pollutants Portable equipment Proteins Reagents Separation Silica Silicon dioxide Sodium Sodium dodecyl sulfate Sodium lauryl sulfate Solutes Stationary phase Surfactants Sustainable development Tubes |
title | Liquid chromatography with micelles in open-tube capillaries |
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