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dc.contributor.authorPark, Kyeng Min-
dc.contributor.authorBaek, Kangkyun-
dc.contributor.authorKo, Young Ho-
dc.contributor.authorShrinidhi, Annadka-
dc.contributor.authorMurray, James-
dc.contributor.authorJang, Won Hyuk-
dc.contributor.authorKim, Ki Hean-
dc.contributor.authorLee, Jun-Seok-
dc.contributor.authorYoo, Jejoong-
dc.contributor.authorKim, Sungwan-
dc.contributor.authorKim, Kimoon-
dc.date.accessioned2024-01-19T23:04:11Z-
dc.date.available2024-01-19T23:04:11Z-
dc.date.created2021-08-31-
dc.date.issued2018-03-12-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121608-
dc.description.abstractSerendipitously, mono-allyloxylated cucurbit[7]uril (AO(1)CB[7]) was discovered to act as an unconventional amphiphile which self-assembles into light-responsive vesicles (AO(1)CB[7]VC) in water. Although the mono-allyloxy group, directly tethered on the periphery of CB[7], is much shorter (C4) than the hydrophobic tails of conventional amphiphiles, it played an important role in vesicle formation. Light-activated transformation of the allyloxy group by conjugation with glutathione was exploited as a remote tool to disrupt the vesicle. The vesicle showed on-demand release of cargo upon irradiation by a laser, after they were internalized into cancer cells. This result demonstrated the potential of AO(1)CB[7]VC as a new type of light-responsive intracellular delivery vehicle for the release of therapeutic cargo, within cells, on demand.-
dc.languageEnglish-
dc.publisherJohn Wiley & Sons Ltd.-
dc.subjectMOLECULAR RECOGNITION-
dc.subjectPHOTODYNAMIC THERAPY-
dc.subjectDRUG-DELIVERY-
dc.subjectFRET PAIR-
dc.subjectFUSION-
dc.subjectNANOPARTICLES-
dc.subjectCOMPLEXES-
dc.subjectCHEMISTRY-
dc.subjectPROTEINS-
dc.subjectPOLYMER-
dc.titleMono-allyloxylated Cucurbit[7]uril Acts as an Unconventional Amphiphile To Form Light-Responsive Vesicles-
dc.typeArticle-
dc.identifier.doi10.1002/anie.201713059-
dc.description.journalClass1-
dc.identifier.bibliographicCitationAngewandte Chemie International Edition, v.57, no.12, pp.3132 - 3136-
dc.citation.titleAngewandte Chemie International Edition-
dc.citation.volume57-
dc.citation.number12-
dc.citation.startPage3132-
dc.citation.endPage3136-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000426759900021-
dc.identifier.scopusid2-s2.0-85042217290-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusMOLECULAR RECOGNITION-
dc.subject.keywordPlusPHOTODYNAMIC THERAPY-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusFRET PAIR-
dc.subject.keywordPlusFUSION-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordAuthoramphiphiles-
dc.subject.keywordAuthorcucurbiturils-
dc.subject.keywordAuthordrug delivery-
dc.subject.keywordAuthorsupramolecular chemistry-
dc.subject.keywordAuthorvesicles-
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KIST Article > 2018
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