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hal.structure.identifierKAUST, Adv Membranes & Porous Mat Ctr
dc.contributor.authorYAN, Jingjing
hal.structure.identifierKAUST, Adv Membranes & Porous Mat Ctr
dc.contributor.authorGUO, Yong
hal.structure.identifierKAUST, Chem & Like Sci & Engn Div
dc.contributor.authorALTAWASHI, Azza
hal.structure.identifierKAUST, Adv Membranes & Porous Mat Ctr
dc.contributor.authorMOOSA, Basem
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorLECOMMANDOUX, Sebastien
hal.structure.identifierKAUST, Adv Membranes & Porous Mat Ctr
dc.contributor.authorKHASHAB, Niveen M.
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2012
dc.identifier.issn1144-0546
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20358
dc.description.abstractEnNanodiamond (ND) and its derivatives have been widely used for drug, protein and gene delivery. Herein, experimental and theoretical methods have been combined to investigate the effect of pH on the delivery of doxorubicin (DOX) from fluorescein labeled NDs (Fc-NDs). In the endosomal recycling process, the nanoparticle will pass from mildly acidic vesicle to pH approximate to 4.8; thus, it is important to investigate DOX release from NDs at different pH values. Fc-NDs released DOX dramatically under acidic conditions, while an increase in the DOX loading efficiency (up to 6.4 wt%) was observed under basic conditions. Further theoretical calculations suggest that H+ weakens the electrostatistic interaction between ND surface carboxyl groups and DOX amino groups, and the interaction energies at pH < 7, pH 7 and pH > 7 are 10.4 kcal mol(-1), 25.0 kcal mol(-1) and 27.0 kcal mol(-1) respectively. Cellular imaging experiments show that Fc-NDs are readily ingested by breast adenocarcinoma (BA) cells and cell viability tests prove that they can be utilized as a safe drug delivery vehicle. Furthermore, pH triggered DOX release has been tested in vitro (pH 7.4 and pH 4.83) in breast adenocarcinoma (BA) cells.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.subject.enDIAMOND NANOPARTICLES
dc.subject.enBIOLOGICAL APPLICATIONS
dc.subject.enDELIVERY-SYSTEM
dc.subject.enCELLS
dc.subject.enSURFACE
dc.subject.enCYTOTOXICITY
dc.subject.enCHEMISTRY
dc.subject.enCANCER
dc.title.enExperimental and theoretical evaluation of nanodiamonds as pH triggered drug carriers
dc.typeArticle de revue
dc.identifier.doi10.1039/c2nj40226b
dc.subject.halChimie/Polymères
bordeaux.journalNew Journal of Chemistry
bordeaux.page1479-1484
bordeaux.volume36
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue7
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00948942
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00948942v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=New%20Journal%20of%20Chemistry&amp;rft.date=2012&amp;rft.volume=36&amp;rft.issue=7&amp;rft.spage=1479-1484&amp;rft.epage=1479-1484&amp;rft.eissn=1144-0546&amp;rft.issn=1144-0546&amp;rft.au=YAN,%20Jingjing&amp;GUO,%20Yong&amp;ALTAWASHI,%20Azza&amp;MOOSA,%20Basem&amp;LECOMMANDOUX,%20Sebastien&amp;rft.genre=article


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