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Alendronate-Modified Hydroxyapatite Nanoparticles for Bone-Specific Dual Delivery of Drug and Bone Mineral

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dc.contributor.authorHwang, Seok-Joon-
dc.contributor.authorLee, Ji-Seon-
dc.contributor.authorRyu, Tae-Kyung-
dc.contributor.authorKang, Rae-Hyung-
dc.contributor.authorJeong, Ki-Young-
dc.contributor.authorJun, Dae-Ryong-
dc.contributor.authorKoh, Jung-Min-
dc.contributor.authorKim, Sung-Eun-
dc.contributor.authorChoi, Sung-Wook-
dc.date.accessioned2021-09-03T22:16:27Z-
dc.date.available2021-09-03T22:16:27Z-
dc.date.created2021-06-18-
dc.date.issued2016-07-
dc.identifier.issn1598-5032-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/88144-
dc.description.abstractAlendronate (Alen)-modified hydroxyapatite (HAp) nanoparticles with multilayers of poly(allylamine) (PAA) and alginate (ALG) were fabricated for bone-specific dual delivery of drug and mineral. Negatively charged HAp nanoparticles were coated with three layers of PAA and ALG using a layer-by-layer (LbL) method and then conjugated with Alen at the outmost layer of the LbL-coated HAp nanoparticles via carbodiimide chemistry. Alen-modified HAp nanoparticles had a spherical morphology and an average size of 61.5 nm. The superior adsorption property of the Alen-modified HAp nanoparticles was quantitatively confirmed using tricalcium phosphate disks as a bone model, compared to HAp nanoparticles. Cell culture assays revealed a higher proliferation rate and alkaline phosphatase activity of osteoblasts treated with the Alen-modified HAp nanoparticles.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER-
dc.subjectSURFACE-ROUGHNESS-
dc.subjectCELL-ADHESION-
dc.subjectIN-VITRO-
dc.subjectBISPHOSPHONATES-
dc.subjectOSTEOPOROSIS-
dc.subjectTITANIUM-
dc.subjectPROLIFERATION-
dc.subjectOSTEOBLASTS-
dc.subjectPROTEIN-
dc.subjectVIVO-
dc.titleAlendronate-Modified Hydroxyapatite Nanoparticles for Bone-Specific Dual Delivery of Drug and Bone Mineral-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Sung-Eun-
dc.identifier.doi10.1007/s13233-016-4094-5-
dc.identifier.scopusid2-s2.0-84976487063-
dc.identifier.wosid000382336000007-
dc.identifier.bibliographicCitationMACROMOLECULAR RESEARCH, v.24, no.7, pp.623 - 628-
dc.relation.isPartOfMACROMOLECULAR RESEARCH-
dc.citation.titleMACROMOLECULAR RESEARCH-
dc.citation.volume24-
dc.citation.number7-
dc.citation.startPage623-
dc.citation.endPage628-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002128912-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusSURFACE-ROUGHNESS-
dc.subject.keywordPlusCELL-ADHESION-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusBISPHOSPHONATES-
dc.subject.keywordPlusOSTEOPOROSIS-
dc.subject.keywordPlusTITANIUM-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusOSTEOBLASTS-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusVIVO-
dc.subject.keywordAuthoralendronate-
dc.subject.keywordAuthorhydroxyapatite-
dc.subject.keywordAuthorlayer-by-layer method-
dc.subject.keywordAuthordual targeted delivery-
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