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dc.contributor.author이지수-
dc.date.accessioned2021-10-22T08:06:50Z-
dc.date.available2021-10-22T08:06:50Z-
dc.date.issued2020-02-
dc.identifier.citationColloids and Surfaces B: Biointerfaces, v. 186, article no. 110702en_US
dc.identifier.issn0927-7765-
dc.identifier.issn1873-4367-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S092777651930846X?via%3Dihub-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/165663-
dc.description.abstractThe objective of this study was to investigate the effects of the particle size of resveratrol (RSV)-loaded nanoparticles (NPs) on their solubility and stability and to optimize their preparation conditions for their solubility and stability. RSV-loaded NPs were prepared using chitosan and γ-poly(glutamic acid) (γ-PGA). Although the solubility and stability of RSV have been significantly increased using chitosan/γ-PGA nanoencapsulation, as the NP size decreased, the solubility increased, but the stability decreased. In order to understand the interrelationship of particle size, solubility, and stability, the target values of RSV solubility and ultraviolet (UV) stability for the aforementioned optimization were determined at two levels: solubility ˃153 μg/mL, UV stability ˃12 % (S153U12) and solubility ˃150 μg/mL, UV stability ˃18 % (S150U18). The S150U18-NPs (258 nm) showed a significantly higher UV stability and tyrosinase inhibition activity against UVA than S153U12-NPs (87 nm) (p ˂ 0.01). Although insignificant, the S153U12-NPs exhibited higher solubility than the S150U18-NPs. In addition, the cellular antioxidant activity was significantly higher in the S153U12-NPs than the S150U18-NPs (p ˂ 0.05). These results demonstrated that the solubility and stability of RSV-loaded NPs may be influenced by their particle size, which could be controlled by the chitosan and γ-PGA concentrations.en_US
dc.description.sponsorshipThis work was supported by the Technological Innovation R&D Program (52230695) funded by the Small and Medium Business Administration (SMBA, Korea).en_US
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.subjectResveratrolen_US
dc.subjectSolubilityen_US
dc.subjectStabilityen_US
dc.subjectParticle sizeen_US
dc.subjectResponse surface methodologyen_US
dc.subjectNanoencapsulationen_US
dc.titleResveratrol-loaded chitosan–γ-poly(glutamic acid) nanoparticles: Optimization, solubility, UV stability, and cellular antioxidant activityen_US
dc.typeArticleen_US
dc.relation.volume186-
dc.identifier.doi10.1016/j.colsurfb.2019.110702-
dc.relation.page110702-110708-
dc.relation.journalColloids and Surfaces B: Biointerfaces-
dc.contributor.googleauthorChung, Joo Hee-
dc.contributor.googleauthorLee, Ji-Soo-
dc.contributor.googleauthorLee, Hyeon Gyu-
dc.relation.code2020004754-
dc.sector.campusS-
dc.sector.daehakRESEARCH INSTITUTE[S]-
dc.sector.departmentKOREAN LIVING SCIENCE RESEARCH INSTITUTE-
dc.identifier.pidiamjisoo-
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RESEARCH INSTITUTE[S](부설연구소) > KOREAN LIVING SCIENCE RESEARCH INSTITUTE(한국생활과학연구소) > Articles
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