Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2154
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dc.contributor.authorGAVVALA, KRISHNAen_US
dc.contributor.authorSatpathi, Sagaren_US
dc.contributor.authorHAZRA, PARTHAen_US
dc.date.accessioned2019-03-15T11:22:38Z
dc.date.available2019-03-15T11:22:38Z
dc.date.issued2015-11en_US
dc.identifier.citationRSC Advances, 5(119), 98080-98086.en_US
dc.identifier.issn2046-2069en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2154-
dc.identifier.urihttps://doi.org/10.1039/C5RA19839Aen_US
dc.description.abstractEllipticine, a well known anticancer drug, emits intense green color when it is intercalated in DNA. It exhibits blue color inside the nano-cavity of a supramolecular host, γ-cyclodextrin (γ-CD). Inspired by these unique fluorescence switching properties of the anticancer drug, in the present work we have monitored the interplay of the drug between γ-CD and DNA by varying the medium pH as a stimulus. Here, steady-state and picosecond time-resolved fluorescence as well as circular dichroism techniques are employed to decipher the location of the drug inside the γ-CD nano-cavity and DNA. Our results confirm that at higher pH the drug selectively stays at γ-CD, even in the presence of biopolymers and exhibits blue color; whereas at lower pH, it is preferentially located in DNA even in the presence of γ-CD and emits a green color. We believe this kind of pH driven translocation of drugs monitored by fluorescence switching may find possible applications in controlled release of the drug inside cells.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectpH responsiveen_US
dc.subjectCyclodextrinen_US
dc.subjectDNAen_US
dc.subjectCircular dichroismen_US
dc.subjectDrug delivery processen_US
dc.subject2015en_US
dc.titlepH responsive translocation of an anticancer drug between cyclodextrin and DNAen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleRSC Advancesen_US
dc.publication.originofpublisherForeignen_US
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