Please use this identifier to cite or link to this item: https://doi.org/10.1021/acs.biomac.7b01176
DC FieldValue
dc.titleEXOPLEXs: Chimeric Drug Delivery Platform from the Fusion of Cell-Derived Nanovesicles and Liposomes
dc.contributor.authorGoh W.J.
dc.contributor.authorZou S.
dc.contributor.authorLee C.K.
dc.contributor.authorOu Y.-H.
dc.contributor.authorWang J.-W.
dc.contributor.authorCzarny B.
dc.contributor.authorPastorin G.
dc.date.accessioned2018-08-29T09:00:28Z
dc.date.available2018-08-29T09:00:28Z
dc.date.issued2018-01-08
dc.identifier.citationGoh W.J., Zou S., Lee C.K., Ou Y.-H., Wang J.-W., Czarny B., Pastorin G. (2018-01-08). EXOPLEXs: Chimeric Drug Delivery Platform from the Fusion of Cell-Derived Nanovesicles and Liposomes. Biomacromolecules 19 (1) : 22-30. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.biomac.7b01176
dc.identifier.issn15257797
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/146747
dc.description.abstractCell-derived nanovesicles (CDNs) have been recently investigated as novel drug delivery systems (DDSs), due to the preservation of key features from the cell membrane of their precursor cells, which are responsible for an efficient cellular uptake by target cells. However, CDNs suffer from low drug loading efficiencies as well as challenges in functionalization compared to conventional DDS like liposomes. Here, we describe the first study proposing the fusion of CDNs with liposomes to form EXOPLEXs. We report the preservation of cell membranes from precursor cells similarly to CDNs, as well as high loading efficiencies of more than 65% with doxorubicin hydrochloride, a model chemotherapeutic drug. The doxorubicin-loaded EXOPLEXs (DOX-EXO) also demonstrated a higher in vitro cell killing effect than liposomes, while EXOPLEXs alone did not show any remarkable cytotoxicity. Taken together, these results illustrate the potential of EXOPLEXs as a novel DDS for targeted delivery of chemotherapeutics. � 2017 American Chemical Society.
dc.publisherAmerican Chemical Society
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentSURGERY
dc.description.doi10.1021/acs.biomac.7b01176
dc.description.sourcetitleBiomacromolecules
dc.description.volume19
dc.description.issue1
dc.description.page22-30
dc.description.codenBOMAF
dc.published.statepublished
dc.grant.idR-148-000-227-720
dc.grant.idR-148-000-213-112
dc.grant.fundingagencyNUS, National University of Singapore
dc.grant.fundingagencyMSE, David O. McKay School of Education, Brigham Young University
dc.grant.fundingagencyNTU, Nanyang Technological University
dc.grant.fundingagencyAlzheimer Society of B.C.
dc.grant.fundingagencySchool of Medicine
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