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Incorporation of Glycine max Merrill Extract into Layered Double Hydroxide through Ion-Exchange and Reconstruction

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dc.contributor.authorJeung, Do-Gak-
dc.contributor.authorKim, Hyoung-Jun-
dc.contributor.authorOh, Jae-Min-
dc.date.accessioned2023-04-28T02:41:06Z-
dc.date.available2023-04-28T02:41:06Z-
dc.date.issued2019-09-
dc.identifier.issn2079-4991-
dc.identifier.issn2079-4991-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/7725-
dc.description.abstractWe incorporated extract of Glycine max Merrill (GM), which is generally known as soybean, into a layered double hydroxide (LDH) nanostructure through two different methods, ion-exchange and reconstruction. Through X-ray diffraction, field-emission scanning electron microscopy, and zeta-potential measurement, GM moiety seemed to be simply attached on the surface of LDH by ion-exchange process, while the extract could be incorporated in the inter-particle pore of LDHs by reconstruction reaction. The quantification exhibited that both incorporation method showed comparable extract loading capacity of 15.6 wt/wt% for GM-LDH hybrid prepared by ion-exchange (GML-I) and 18.6 wt/wt% for GM-LDH hybrid by reconstruction (GML-R). On the other hand, bioactive substance in both GM-LDH hybrids, revealed that GML-R has higher daidzein content (0.0286 wt/wt%) compared with GML-I (0.0108 wt/wt%). According to time-dependent daidzein release, we confirmed that GML-R showed pH dependent daidzein release; a higher amount of daidzein was released in pH 4.5 physiological condition than in pH 7.4, suggesting the drug delivery potential of GML-R. Furthermore, alkaline phosphatase activity and collagen fiber formation on human osteoblast-like MG-63 cells displayed that GML-R had superior possibility of osteoblast differentiation than GML-I. From these results, we concluded that reconstruction method was more effective for extract incorporation than ion-exchange reaction, due to its pH dependent release property and alkaline phosphatase activity.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleIncorporation of Glycine max Merrill Extract into Layered Double Hydroxide through Ion-Exchange and Reconstruction-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/nano9091262-
dc.identifier.scopusid2-s2.0-85073315776-
dc.identifier.wosid000489101900079-
dc.identifier.bibliographicCitationNANOMATERIALS, v.9, no.9-
dc.citation.titleNANOMATERIALS-
dc.citation.volume9-
dc.citation.number9-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusDRUG-DELIVERY SYSTEM-
dc.subject.keywordPlusCONTROLLED-RELEASE-
dc.subject.keywordPlusCALCAREOUS SOILS-
dc.subject.keywordPlusCELLULAR UPTAKE-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusINTERCALATION-
dc.subject.keywordPlusDAIDZEIN-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusAVAILABILITY-
dc.subject.keywordPlusKINETICS-
dc.subject.keywordAuthorlayered double hydroxide-
dc.subject.keywordAuthorGlycine max Merrill extract-
dc.subject.keywordAuthorincorporation method-
dc.subject.keywordAuthorrelease-
dc.subject.keywordAuthoralkaline phosphatase activity-
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