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dc.contributor.authorYoung, Jenn-jongen_US
dc.contributor.authorCheng, Kuang-mingen_US
dc.contributor.authorYoung, Yen-anen_US
dc.contributor.authorChen, Xin-anen_US
dc.contributor.authorChen, Yu-haoen_US
dc.contributor.authorChang, Tein-yaoen_US
dc.contributor.authorYen, Hui-juen_US
dc.contributor.authorChen, Cheng-cheungen_US
dc.date.accessioned2018-08-21T05:53:21Z-
dc.date.available2018-08-21T05:53:21Z-
dc.date.issued2018-03-02en_US
dc.identifier.issn0008-6215en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.carres.2017.12.004en_US
dc.identifier.urihttp://hdl.handle.net/11536/144584-
dc.description.abstractHerein, we describe an improved procedure for the green synthesis of chondroitin sulfate stabilized silver nanoparticles (ChS-AgNPs). Glucose was used as a reducing agent under alkaline conditions to obtain a small particle size (<10 nm), and the reduction was complete within one hour at room temperature. The concentration of NaOH affected the reaction rate, formation yield, and particle size of ChS-AgNPs. The formation of AgNPs was confirmed using UV-vis, TEM, XRD, and XPS. ChS-AgNPs showed excellent catalytic activities in the reduction of 4-nitrophenol by NaBH4, and the reaction rate increased linearly with increasing catalyst amounts. The antimicrobial activities of ChS-AgNPs against A. baumannii (including multidrug-resistant strains), E. coli, P. aeruginosa, and S. aureus were evaluated using the broth microdilution method. Finally, from the morphological observations and cell cycle analysis of L929 cells, we found that ChS-AgNPs exhibited antimicrobial and biocompatible activities. (c) 2017 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectGreen synthesisen_US
dc.subjectSilver nanoparticlesen_US
dc.subjectChondroitin sulfateen_US
dc.subjectCatalytic activityen_US
dc.subjectAntimicrobial and biocompatible activitiesen_US
dc.subjectMultidrug-resistant Acinetobacter baumanniien_US
dc.titleChondroitin sulfate-stabilized silver nanoparticles: Improved synthesis and their catalytic, antimicrobial, and biocompatible activitiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.carres.2017.12.004en_US
dc.identifier.journalCARBOHYDRATE RESEARCHen_US
dc.citation.volume457en_US
dc.citation.spage14en_US
dc.citation.epage24en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000426004100003en_US
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