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Anisotropic Bimetallic Core Satellite-poly(aniline) Nanohybrids for Detection of Autoantibodies

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dc.contributor.authorHwang, Eun Young-
dc.contributor.authorLee, Jae Hee-
dc.contributor.authorLim, Dong Woo-
dc.date.accessioned2023-08-16T07:39:37Z-
dc.date.available2023-08-16T07:39:37Z-
dc.date.issued2020-10-
dc.identifier.issn1022-1336-
dc.identifier.issn1521-3927-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/113985-
dc.description.abstractBimetallic core–satellite nanoparticles are widely exploited in surface-enhanced Raman scattering (SERS)-based applications due to their enhanced optical properties compared to single-component metallic nanoparticles (MNPs). In addition, anisotropic hybrid nanostructures containing both MNPs and polymeric compartments constitute a new class of functional nanomaterials for photonic applications because they show different functionalities and physicochemical characteristics at two distinct compartments. Herein, synthesis of two kinds of anisotropic bimetallic core–satellite–poly(aniline) nanohybrids (ABCPNs) using small or polymeric ligand-coated gold nanospheres or gold nanorods as seeds is reported. The ABCPNs exhibit enhanced optical properties due to a local electromagnetic field generated in the narrow interparticle gap between core and satellite nanoparticles. Furthermore, a SERS-based quantitative analysis of autoantibodies against cyclic citrullinated peptide using the ABCPNs as SERS nanoprobes for a diagnosis of early rheumatoid arthritis is demonstrated, suggesting that these multifunctional nanostructures will be potential for advanced SERS-based biosensors. © 2020 Wiley-VCH GmbH-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleAnisotropic Bimetallic Core Satellite-poly(aniline) Nanohybrids for Detection of Autoantibodies-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/marc.202000331-
dc.identifier.scopusid2-s2.0-85090467284-
dc.identifier.wosid000567646400001-
dc.identifier.bibliographicCitationMacromolecular Rapid Communications, v.41, no.20, pp 331 - 339-
dc.citation.titleMacromolecular Rapid Communications-
dc.citation.volume41-
dc.citation.number20-
dc.citation.startPage331-
dc.citation.endPage339-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusENHANCED RAMAN-SCATTERING-
dc.subject.keywordPlusCORE-SATELLITE NANOSTRUCTURES-
dc.subject.keywordPlusCYCLIC CITRULLINATED PEPTIDE-
dc.subject.keywordPlusCOATED GOLD NANORODS-
dc.subject.keywordPlusEARLY-DIAGNOSIS-
dc.subject.keywordPlusAG-
dc.subject.keywordPlus4-AMINOTHIOPHENOL-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusIMMUNOASSAY-
dc.subject.keywordPlusNANOGAP-
dc.subject.keywordAuthoranisotropy-
dc.subject.keywordAuthorautoantibody detection-
dc.subject.keywordAuthorbimetallic core–satellite-
dc.subject.keywordAuthornanohybrids-
dc.subject.keywordAuthorpoly(aniline)-
dc.subject.keywordAuthorrheumatoid arthritis-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1002/marc.202000331-
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