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dc.contributor.authorYang, CT
dc.contributor.authorPourhassan-Moghaddam, M
dc.contributor.authorWu, L
dc.contributor.authorBai, P
dc.contributor.authorThierry, B
dc.date.accessioned2018-08-26T04:58:10Z
dc.date.available2018-08-26T04:58:10Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/38715
dc.description.abstractThe development of simple yet ultrasensitive biosensing approaches for the detection of cancer prognostic microRNA is an important step toward their successful clinical implementation. We demonstrate the relevance for the detection of circulating miRNA of a novel signal amplification scheme based on surface plasmon resonance enhanced light scattering (SP-LS). In addition to experimental optimization carried out using gold nanoparticle (AuNP) tags conjugated with a monoclonal antibody with high affinity for RNA*DNA hybrid duplexes, simulation modeling was conducted to obtain insights about SP-LS biosensing. SP-LS enabled the detection of miRNA-122 at subpicomolar concentrations within 30 min, and a limit of detection of 2 attomoles (60 fM, 50 ?L) was determined. MiRNA-122 could also be reliably detected in a high concentration background of nontarget miRNA. The proposed SP-LS miRNA detection approach could be readily applied to other miRNA targets of diagnostic importance and further developed to allow for multiplex measurements of miRNA panels. The promising results obtained in this study and advantageous features of SP-LS warrant further development and its application to clinical samples.
dc.language.isoEnglish
dc.relation.ispartofACS sensors
dc.titleUltrasensitive Detection of Cancer Prognostic miRNA Biomarkers Based on Surface Plasmon Enhanced Light Scattering.
dc.typearticle
dc.citation.volume2
dc.citation.issue5
dc.citation.spage635
dc.citation.epage640
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1021/acssensors.6b00776


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