Recognition and Sensing of Creatinine
Current methods for creatinine quantification suffer from significant drawbacks when aiming to combine accuracy, simplicity, and affordability. Here, an unprecedented synthetic receptor, an aryl‐substituted calix[4]pyrrole with a monophosphonate bridge, is reported that displays remarkable affinity...
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Veröffentlicht in: | Angewandte Chemie International Edition 2016-02, Vol.55 (7), p.2435-2440 |
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creator | Guinovart, Tomàs Hernández-Alonso, Daniel Adriaenssens, Louis Blondeau, Pascal Martínez-Belmonte, Marta Rius, F. Xavier Andrade, Francisco J. Ballester, Pablo |
description | Current methods for creatinine quantification suffer from significant drawbacks when aiming to combine accuracy, simplicity, and affordability. Here, an unprecedented synthetic receptor, an aryl‐substituted calix[4]pyrrole with a monophosphonate bridge, is reported that displays remarkable affinity for creatinine and the creatininium cation. The receptor works by including the guest in its deep and polar aromatic cavity and establishing directional interactions in three dimensions. When incorporated into a suitable polymeric membrane, this molecule acts as an ionophore. A highly sensitive and selective potentiometric sensor suitable for the determination of creatinine levels in biological fluids, such as urine or plasma, in an accurate, fast, simple, and cost‐effective way has thus been developed.
Creatinine quantification: A monophosphonate‐bridge calix[4]pyrrole cavitand traps creatinine and the creatininium cation in its deep and polar aromatic cavity. The receptor offers complementary hydrogen‐bonding sites to the polar functional groups of the guest. Its use as an ionophore enhances the analytical performance of ion‐selective electrodes and enables the determination of creatinine levels in biological samples. |
doi_str_mv | 10.1002/anie.201510136 |
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Creatinine quantification: A monophosphonate‐bridge calix[4]pyrrole cavitand traps creatinine and the creatininium cation in its deep and polar aromatic cavity. The receptor offers complementary hydrogen‐bonding sites to the polar functional groups of the guest. Its use as an ionophore enhances the analytical performance of ion‐selective electrodes and enables the determination of creatinine levels in biological samples.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201510136</identifier><identifier>PMID: 26749029</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Affinity ; Aromatic compounds ; Cations ; cavitands ; Creatinine ; Creatinine - analysis ; Creatinine - blood ; Creatinine - urine ; Detection ; Displays ; Fluids ; Holes ; Humans ; ionophores ; molecular recognition ; Proton Magnetic Resonance Spectroscopy ; Recognition ; sensors ; Urine</subject><ispartof>Angewandte Chemie International Edition, 2016-02, Vol.55 (7), p.2435-2440</ispartof><rights>2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5466-788812d3fe92466946086afe411ae39c03928c9483d4a0836f8b7f7bf4466cb03</citedby><cites>FETCH-LOGICAL-c5466-788812d3fe92466946086afe411ae39c03928c9483d4a0836f8b7f7bf4466cb03</cites><orcidid>0000-0001-8377-6610</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%2Fanie.201510136$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.201510136$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26749029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guinovart, Tomàs</creatorcontrib><creatorcontrib>Hernández-Alonso, Daniel</creatorcontrib><creatorcontrib>Adriaenssens, Louis</creatorcontrib><creatorcontrib>Blondeau, Pascal</creatorcontrib><creatorcontrib>Martínez-Belmonte, Marta</creatorcontrib><creatorcontrib>Rius, F. Xavier</creatorcontrib><creatorcontrib>Andrade, Francisco J.</creatorcontrib><creatorcontrib>Ballester, Pablo</creatorcontrib><title>Recognition and Sensing of Creatinine</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>Current methods for creatinine quantification suffer from significant drawbacks when aiming to combine accuracy, simplicity, and affordability. Here, an unprecedented synthetic receptor, an aryl‐substituted calix[4]pyrrole with a monophosphonate bridge, is reported that displays remarkable affinity for creatinine and the creatininium cation. The receptor works by including the guest in its deep and polar aromatic cavity and establishing directional interactions in three dimensions. When incorporated into a suitable polymeric membrane, this molecule acts as an ionophore. A highly sensitive and selective potentiometric sensor suitable for the determination of creatinine levels in biological fluids, such as urine or plasma, in an accurate, fast, simple, and cost‐effective way has thus been developed.
Creatinine quantification: A monophosphonate‐bridge calix[4]pyrrole cavitand traps creatinine and the creatininium cation in its deep and polar aromatic cavity. The receptor offers complementary hydrogen‐bonding sites to the polar functional groups of the guest. Its use as an ionophore enhances the analytical performance of ion‐selective electrodes and enables the determination of creatinine levels in biological samples.</description><subject>Affinity</subject><subject>Aromatic compounds</subject><subject>Cations</subject><subject>cavitands</subject><subject>Creatinine</subject><subject>Creatinine - analysis</subject><subject>Creatinine - blood</subject><subject>Creatinine - urine</subject><subject>Detection</subject><subject>Displays</subject><subject>Fluids</subject><subject>Holes</subject><subject>Humans</subject><subject>ionophores</subject><subject>molecular recognition</subject><subject>Proton Magnetic Resonance Spectroscopy</subject><subject>Recognition</subject><subject>sensors</subject><subject>Urine</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLAzEURoMoVqtblzIggpupeU0ey1JrLZSK1scypNNMSZ1majJF--9NaS3iQle5gfOde_kAOEOwhSDE19pZ08IQZQgiwvbAEcowSgnnZD_OlJCUiww1wHEIs8gLAdkhaGDGqYRYHoHLR5NXU2drW7lEu0kyMi5YN02qIul4o2vrrDMn4KDQZTCn27cJnm-7T527dHDf63fagzTPKGNxlRAIT0hhJI5_SRkUTBeGIqQNkTkkEotcUkEmVENBWCHGvODjgkY6H0PSBFcb78JX70sTajW3ITdlqZ2plkEhzrBklPA1evELnVVL7-J1CknIGEQ0y_6kogtRwTISqdaGyn0VgjeFWng7136lEFTrmtW6ZrWrOQbOt9rleG4mO_y71wjIDfBhS7P6R6faw373pzzdZG2ozecuq_2bYpzwTL0Oewo_yOHo5QYqSb4AXGOTrA</recordid><startdate>20160212</startdate><enddate>20160212</enddate><creator>Guinovart, Tomàs</creator><creator>Hernández-Alonso, Daniel</creator><creator>Adriaenssens, Louis</creator><creator>Blondeau, Pascal</creator><creator>Martínez-Belmonte, Marta</creator><creator>Rius, F. Xavier</creator><creator>Andrade, Francisco J.</creator><creator>Ballester, Pablo</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7TM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8377-6610</orcidid></search><sort><creationdate>20160212</creationdate><title>Recognition and Sensing of Creatinine</title><author>Guinovart, Tomàs ; Hernández-Alonso, Daniel ; Adriaenssens, Louis ; Blondeau, Pascal ; Martínez-Belmonte, Marta ; Rius, F. Xavier ; Andrade, Francisco J. ; Ballester, Pablo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5466-788812d3fe92466946086afe411ae39c03928c9483d4a0836f8b7f7bf4466cb03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Affinity</topic><topic>Aromatic compounds</topic><topic>Cations</topic><topic>cavitands</topic><topic>Creatinine</topic><topic>Creatinine - analysis</topic><topic>Creatinine - blood</topic><topic>Creatinine - urine</topic><topic>Detection</topic><topic>Displays</topic><topic>Fluids</topic><topic>Holes</topic><topic>Humans</topic><topic>ionophores</topic><topic>molecular recognition</topic><topic>Proton Magnetic Resonance Spectroscopy</topic><topic>Recognition</topic><topic>sensors</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guinovart, Tomàs</creatorcontrib><creatorcontrib>Hernández-Alonso, Daniel</creatorcontrib><creatorcontrib>Adriaenssens, Louis</creatorcontrib><creatorcontrib>Blondeau, Pascal</creatorcontrib><creatorcontrib>Martínez-Belmonte, Marta</creatorcontrib><creatorcontrib>Rius, F. Xavier</creatorcontrib><creatorcontrib>Andrade, Francisco J.</creatorcontrib><creatorcontrib>Ballester, Pablo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guinovart, Tomàs</au><au>Hernández-Alonso, Daniel</au><au>Adriaenssens, Louis</au><au>Blondeau, Pascal</au><au>Martínez-Belmonte, Marta</au><au>Rius, F. Xavier</au><au>Andrade, Francisco J.</au><au>Ballester, Pablo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recognition and Sensing of Creatinine</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2016-02-12</date><risdate>2016</risdate><volume>55</volume><issue>7</issue><spage>2435</spage><epage>2440</epage><pages>2435-2440</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>Current methods for creatinine quantification suffer from significant drawbacks when aiming to combine accuracy, simplicity, and affordability. Here, an unprecedented synthetic receptor, an aryl‐substituted calix[4]pyrrole with a monophosphonate bridge, is reported that displays remarkable affinity for creatinine and the creatininium cation. The receptor works by including the guest in its deep and polar aromatic cavity and establishing directional interactions in three dimensions. When incorporated into a suitable polymeric membrane, this molecule acts as an ionophore. A highly sensitive and selective potentiometric sensor suitable for the determination of creatinine levels in biological fluids, such as urine or plasma, in an accurate, fast, simple, and cost‐effective way has thus been developed.
Creatinine quantification: A monophosphonate‐bridge calix[4]pyrrole cavitand traps creatinine and the creatininium cation in its deep and polar aromatic cavity. The receptor offers complementary hydrogen‐bonding sites to the polar functional groups of the guest. Its use as an ionophore enhances the analytical performance of ion‐selective electrodes and enables the determination of creatinine levels in biological samples.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>26749029</pmid><doi>10.1002/anie.201510136</doi><tpages>6</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0001-8377-6610</orcidid></addata></record> |
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subjects | Affinity Aromatic compounds Cations cavitands Creatinine Creatinine - analysis Creatinine - blood Creatinine - urine Detection Displays Fluids Holes Humans ionophores molecular recognition Proton Magnetic Resonance Spectroscopy Recognition sensors Urine |
title | Recognition and Sensing of Creatinine |
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