Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/104444
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dc.contributorDepartment of Industrial and Systems Engineeringen_US
dc.creatorWang, Xen_US
dc.creatorLiu, Cen_US
dc.creatorLi, Zen_US
dc.creatorTang, CYen_US
dc.creatorLaw, WCen_US
dc.creatorGong, Xen_US
dc.creatorLiu, Zen_US
dc.creatorLiao, Yen_US
dc.creatorZhang, Gen_US
dc.creatorLong, Sen_US
dc.creatorChen, Len_US
dc.date.accessioned2024-02-05T08:49:57Z-
dc.date.available2024-02-05T08:49:57Z-
dc.identifier.issn1932-7447en_US
dc.identifier.urihttp://hdl.handle.net/10397/104444-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2019 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Physical Chemistry C, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jpcc.9b00454.en_US
dc.titleThermal and photo dual-responsive core–shell polymeric nanocarriers with encapsulation of upconversion nanoparticles for controlled anticancer drug releaseen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage10658en_US
dc.identifier.epage10665en_US
dc.identifier.volume123en_US
dc.identifier.issue16en_US
dc.identifier.doi10.1021/acs.jpcc.9b00454en_US
dcterms.abstractA thermal and photo dual-responsive drug delivery system is newly designed for controlled anticancer drug delivery. The concept of this design is to encapsulate upconversion nanoparticles in a photoresponsive polymer to produce core–shell nanoparticles, in which NIR light is converted to UV/visible light to isomerize cross-linked bis(methacryloylamino)-azobenzene for the control of drug release. A facile scheme, which gives the details of two-step solvothermal treatment, microemulsion, distillation precipitation polymerization, and drug loading, is proposed to realize the design. The dual-responsive drug release behaviors of the system are reported to provide the information for potential development of cancer therapy. It is also found that the Baker–Lonsdale model is suitable for describing the drug release kinetics of this system and the values of the diffusion coefficient under various conditions are determined experimentally.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of physical chemistry C, 25 Apr. 2019, v. 123, no. 16, p. 10658-10665en_US
dcterms.isPartOfJournal of physical chemistry Cen_US
dcterms.issued2019-04-25-
dc.identifier.scopus2-s2.0-85065023615-
dc.identifier.eissn1932-7455en_US
dc.description.validate202402 bcchen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberISE-0482-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNatural National Science Foundation of China; The Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS25066549-
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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