Target delivery of beta-cyclodextrin/paclitaxel complexed fluorescent carbon nanoparticles: externally NIR light and internally pH sensitive-mediated release of paclitaxel with bio-imaging

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dc.contributor.authorSharker, Shazid Md.ko
dc.contributor.authorKim, Sung Minko
dc.contributor.authorKim, Sung Hanko
dc.contributor.authorIn, Insikko
dc.contributor.authorLee, Haeshinko
dc.contributor.authorPark, Sung Youngko
dc.date.accessioned2015-11-20T07:28:42Z-
dc.date.available2015-11-20T07:28:42Z-
dc.date.created2015-08-10-
dc.date.created2015-08-10-
dc.date.issued2015-07-
dc.identifier.citationJOURNAL OF MATERIALS CHEMISTRY B, v.3, no.28, pp.5833 - 5841-
dc.identifier.issn2050-750X-
dc.identifier.urihttp://hdl.handle.net/10203/200691-
dc.description.abstractThe development of cooperative drug delivery systems that can detect and target the disease site, with rapid trigger controlled drug release (internally and externally), is widely expected to change the landscape of future drug carriers. In this study a drug delivery system was developed for the cancer-targeted release of chemotherapeutic agents inside living cells. This system is an environment sensitive (pH), and external photothermally remote controlled, cooperative image-guided drug delivery matrix. Partially carbonized fluorescence hyaluronic acid (HA-FCN) was conjugated with boronic acid (BA) to promote the formation of boronate ester with diol groups of beta-cyclodextrin (CD) [HA-FCN-CD]. The pH influence mediated release of paclitaxel (PTX) from the CD cavity of HA-FCN-CD was utilized for targeted cancer bioimaging. This active-target delivery system (HA-FCN-CD-PTX) was found to show optical absorption properties similar to those of the near infrared (NIR) light sensitive carbonized material. This system exploits acidity for triggered drug release and rapid generation of mild photothermal heat to trigger burst release of PTX. Cooperative guided bioimaging that employs both internal pH responsive and external NIR controlled drug carriers is a promising method for chemotherapeutic release that can be adjusted according to physiological needs-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectREDUCED GRAPHENE OXIDE-
dc.subjectDRUG-DELIVERY-
dc.subjectRESPONSIVE NANOPARTICLES-
dc.subjectINTRACELLULAR DELIVERY-
dc.subjectCANCER NANOTECHNOLOGY-
dc.subjectTHERAPY-
dc.subjectDOTS-
dc.subjectPOLYMER-
dc.subjectSYSTEMS-
dc.titleTarget delivery of beta-cyclodextrin/paclitaxel complexed fluorescent carbon nanoparticles: externally NIR light and internally pH sensitive-mediated release of paclitaxel with bio-imaging-
dc.typeArticle-
dc.identifier.wosid000357830600020-
dc.identifier.scopusid2-s2.0-84936971417-
dc.type.rimsART-
dc.citation.volume3-
dc.citation.issue28-
dc.citation.beginningpage5833-
dc.citation.endingpage5841-
dc.citation.publicationnameJOURNAL OF MATERIALS CHEMISTRY B-
dc.identifier.doi10.1039/c5tb00779h-
dc.contributor.localauthorLee, Haeshin-
dc.contributor.nonIdAuthorKim, Sung Min-
dc.contributor.nonIdAuthorKim, Sung Han-
dc.contributor.nonIdAuthorIn, Insik-
dc.contributor.nonIdAuthorPark, Sung Young-
dc.type.journalArticleArticle-
dc.subject.keywordPlusREDUCED GRAPHENE OXIDE-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusRESPONSIVE NANOPARTICLES-
dc.subject.keywordPlusINTRACELLULAR DELIVERY-
dc.subject.keywordPlusCANCER NANOTECHNOLOGY-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusDOTS-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordPlusSYSTEMS-
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