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dc.contributor.authorChuang, Chun-Chiaoen_US
dc.contributor.authorCheng, Chih-Chien_US
dc.contributor.authorChen, Pei-Yingen_US
dc.contributor.authorLo, Chiehen_US
dc.contributor.authorChen, Yi-Ningen_US
dc.contributor.authorShih, Min-Hsiungen_US
dc.contributor.authorChang, Chien-Wenen_US
dc.date.accessioned2019-04-02T05:58:20Z-
dc.date.available2019-04-02T05:58:20Z-
dc.date.issued2019-01-01en_US
dc.identifier.issn1178-2013en_US
dc.identifier.urihttp://dx.doi.org/10.2147/IJN.S177851en_US
dc.identifier.urihttp://hdl.handle.net/11536/148637-
dc.description.abstractPurpose: A biocompatible nanocomplex system co-encapsulated with gold nanorods (AuNRs) and doxorubicin (DOX) was investigated for its potentials on the combined photothermal- and chemotherapy. Materials and methods: Hydrophobic AuNRs were synthesized by the hexadecyltrimethyl-ammonium bromide (CTAB)-mediated seed growth method, and then, they received two-step surface modifications of polyethylene glycol (PEG) and dodecane. The AuNR/DOX/poly(lactic-co-glycolic acid) (PLGA) nanocomplexes were prepared by emulsifying DOX, AuNR, and PLGA into aqueous polyvinyl alcohol solution by sonication. Human serum albumin (HSA) was used to coat the nanocomplexes to afford HSA/AuNR/DOX-PLGA (HADP). Size and surface potential of the HADP nanocomplexes were determined by using a Zetasizer. Cytotoxicity and cellular uptake of the HADP were analyzed by using MTT assay and flow cytometry, respectively. In vitro anticancer effects of the HADP were studied on various cancer cell lines. To assess the therapeutic efficacy, CT26 tumor-bearing mice were intravenously administered with HADP nanocomplexes and laser treatments, followed by monitoring of the tumor growth and body weight. Results: Size and surface potential of the HADP nanocomplexes were 245.8 nm and -8.6 mV, respectively. Strong photothermal effects were verified on the AuNR-loaded PLGA nanoparticles (NPs) in vitro. Rapid and repeated drug release from the HADP nanocomplexes was successfully achieved by near-infrared (NIR) irradiations. HSA significantly promoted cellular uptake of the HADP nanocomplexes to murine colon cancer cells as demonstrated by cell imaging and flow cytometric studies. By combining photothermal and chemotherapy, the HADP nanocomplexes exhibited strong synergistic anticancer effects in vitro and in vivo. Conclusion: An NIR-triggered drug release system by encapsulating hydrophobic AuNR and DOX inside the PLGA NPs has been successfully prepared in this study. The HADP NPs show promising combined photothermal- and chemotherapeutic effects without inducing undesired side effects on a murine colon cancer animal model.en_US
dc.language.isoen_USen_US
dc.subjectgold nanomaterialsen_US
dc.subjectphotothermal therapyen_US
dc.subjecttriggered drug releaseen_US
dc.subjectalbuminen_US
dc.subjectbiodegradable nanoparticlesen_US
dc.titleGold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapyen_US
dc.typeArticleen_US
dc.identifier.doi10.2147/IJN.S177851en_US
dc.identifier.journalINTERNATIONAL JOURNAL OF NANOMEDICINEen_US
dc.citation.volume14en_US
dc.citation.spage181en_US
dc.citation.epage193en_US
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:000454359600005en_US
dc.citation.woscount0en_US
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