Mesoporous silica-supported platinum nanocatalysts for colorimetric detection of glucose, cholesterol, and C-reactive protein
DC Field | Value | Language |
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dc.contributor.author | Kim, Taehyeong | - |
dc.contributor.author | Kim, Dokyoon | - |
dc.date.accessioned | 2024-09-05T08:00:56Z | - |
dc.date.available | 2024-09-05T08:00:56Z | - |
dc.date.issued | 2024-07 | - |
dc.identifier.issn | 1477-9226 | - |
dc.identifier.issn | 1477-9234 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/120424 | - |
dc.description.abstract | Noble metal nanoparticles decorated on a catalyst support with a large specific surface area can exhibit enhanced catalytic activity. To this end, a synthetic method to heterogeneously and evenly nucleate platinum nanoparticles (Pt NPs) onto mesoporous silica nanoparticles (MSNs) is developed. The obtained Pt NP-modified MSNs (Pt-MSNs) are characterized as a thin layer of 3 nm-sized Pt NPs densely assembled on the MSN surface, by which the throughput of the peroxidase-like activity of Pt-MSNs is greatly improved. The utility of Pt-MSNs in colorimetric detection of analytes is validated for two different assay schemes. Firstly, colloidally dispersed Pt-MSNs are employed as a peroxidase-mimic in a two-step cascade reaction to quantitate glucose/cholesterol based on the amount of H2O2 produced by glucose/cholesterol oxidase. Secondly, detection of C-reactive protein (CRP) is conducted on a solid substrate by adopting a sandwich immunoassay format. Detection limits are estimated to be 20 μM, 55 μM, and 3.9 pM for glucose, cholesterol, and CRP, respectively. © 2024 The Royal Society of Chemistry. | - |
dc.format.extent | 13 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Royal Society of Chemistry | - |
dc.title | Mesoporous silica-supported platinum nanocatalysts for colorimetric detection of glucose, cholesterol, and C-reactive protein | - |
dc.type | Article | - |
dc.publisher.location | 영국 | - |
dc.identifier.doi | 10.1039/d4dt01534g | - |
dc.identifier.scopusid | 2-s2.0-85199006040 | - |
dc.identifier.wosid | 001271057100001 | - |
dc.identifier.bibliographicCitation | Dalton Transactions, v.53, no.30, pp 1 - 13 | - |
dc.citation.title | Dalton Transactions | - |
dc.citation.volume | 53 | - |
dc.citation.number | 30 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 13 | - |
dc.type.docType | Article in Press | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Inorganic & Nuclear | - |
dc.subject.keywordPlus | HIGHLY EFFICIENT | - |
dc.subject.keywordPlus | HYDROGEN-PEROXIDE | - |
dc.subject.keywordPlus | CARGO DELIVERY | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | NANOPARTICLES | - |
dc.subject.keywordPlus | SIZE | - |
dc.subject.keywordPlus | RELEASE | - |
dc.subject.keywordPlus | OXIDATION | - |
dc.subject.keywordPlus | THERAPY | - |
dc.identifier.url | https://pubs.rsc.org/en/content/articlelanding/2024/dt/d4dt01534g | - |
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