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dc.contributor.authorJyothi B Nair-
dc.contributor.authorMohapatra, S-
dc.contributor.authorGhosh, S-
dc.contributor.authorMaiti, K K-
dc.date.accessioned2015-02-20T04:44:49Z-
dc.date.available2015-02-20T04:44:49Z-
dc.date.issued2015-
dc.identifier.citationChemical Communications 51(12):2403-6;27 Jan 2015en_US
dc.identifier.issn1364-548X-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1784-
dc.description.abstractAn efficient synthetic approach has been adopted to construct a new dendron-based octa-guanidine appended molecular transporter with a lysosomal targeted peptide-doxorubicin conjugate. The transporter alone (G8-PPI-FL) is found to be non-toxic, showed higher cellular uptake compared to Arg-8-mer and exhibited excellent selectivity towards lysosomes in cathepsin B expressing HeLa cells, while the Dox-conjugate showed significant cytotoxicity to cancer cells without affecting the non-cancerous cells.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectGuanidinium-poly-(propylene imine)en_US
dc.subjectDoxorubicinen_US
dc.subjectCancer cellsen_US
dc.subjectLysosomeen_US
dc.titleNovel lysosome targeted molecular transporter built on a guanidinium-poly-(propylene imine) hybrid dendron for efficient delivery of doxorubicin into cancer cellsen_US
dc.typeArticleen_US
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