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Aggregation-driven fluorescence quenching of imidazole-functionalized perylene diimide for urea sensing

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dc.contributor.authorCho, Junghyun-
dc.contributor.authorKeum, Changjoon-
dc.contributor.authorLee, Sang-Guk-
dc.contributor.authorLee, Sang-Yup-
dc.date.accessioned2020-12-01T18:07:22Z-
dc.date.available2020-12-01T18:07:22Z-
dc.date.created2021-03-18-
dc.date.issued2020-11-
dc.identifier.issn0003-2654-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/180612-
dc.description.abstractStimuli-responsive self-assembly of functional amphiphilic molecules by specific chemical stimulants is a promising strategy for sensor application. Herein, we demonstrate a fast optical detection of urea in human urine by exploiting bolaform perylene diimide functionalized with imidazoles (PDI-Hm), whose aggregation is induced by urea hydrolysis. The hydroxides produced from the enzymatic urea hydrolysis deprotonate the imidazoles to reduce electrostatic repulsion between PDI-Hm molecules in a HCl-methanol mixture, thereby leading to aggregation and consequent fluorescence quenching. The molecular interaction of PDI-Hm was further scrutinized to understand the aggregation behavior driven by the screening of electrical repulsion. As an optical sensing probe, PDI-Hm displays a prompt response (<1 min) to hydroxide and detection limit of 0.4 mM for urea. PDI-Hm incorporating urease offers considerable selectivity toward urea among various components in human urine. The urea sensing accuracy of this PDI-Hm fluorescence chemosensor is comparable to that of a clinical method, showing 93.4% consistency. Furthermore, the PDI-Hm was fabricated into a gel film allowed for the fast screening of excessive urea in urine.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherRoyal Society of Chemistry-
dc.relation.isPartOfANALYST-
dc.relation.isPartOfANALYST-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleAggregation-driven fluorescence quenching of imidazole-functionalized perylene diimide for urea sensing-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Laboratory Medicine (진단검사의학교실)-
dc.contributor.googleauthorCho, Junghyun-
dc.contributor.googleauthorKeum, Changjoon-
dc.contributor.googleauthorLee, Sang-Guk-
dc.contributor.googleauthorLee, Sang-Yup-
dc.identifier.doi10.1039/d0an01252a-
dc.relation.journalcodeJ00130-
dc.identifier.eissn1364-5528-
dc.contributor.alternativeNameLee, Sang Guk-
dc.contributor.affiliatedAuthorLee, Sang-Guk-
dc.identifier.scopusid2-s2.0-85095861462-
dc.identifier.wosid000587582800019-
dc.citation.volume145-
dc.citation.number22-
dc.citation.startPage7312-
dc.citation.endPage7319-
dc.identifier.bibliographicCitationANALYST, Vol.145(22) : 7312-7319, 2020-11-
dc.identifier.rimsid69165-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordPlusELECTROCHEMICAL SENSOR-
dc.subject.keywordPlusNONENZYMATIC DETECTION-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusBISIMIDE-
dc.subject.keywordPlusPH-
dc.subject.keywordPlusSEMICONDUCTOR-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusGRAPHENE-
dc.subject.keywordPlusURINE-
dc.subject.keywordPlusPROBE-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalResearchAreaChemistry-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

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