Multiplexed ultrafast photothermal digital polymerase chain reaction based on oligo(phenylene-ethynylene)

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dc.contributor.authorG J Kim-
dc.contributor.authorK H Kim-
dc.contributor.authorB Lee-
dc.contributor.authorM Han-
dc.contributor.authorS Rho-
dc.contributor.authorS Y Hong-
dc.contributor.authorH K Kim-
dc.contributor.authorS J Park-
dc.contributor.authorW S Yun-
dc.contributor.authorY M Park-
dc.contributor.authorK G Lee-
dc.contributor.authorKyong-Cheol Ko-
dc.contributor.authorO S Kwon-
dc.date.accessioned2025-08-07T16:35:16Z-
dc.date.available2025-08-07T16:35:16Z-
dc.date.issued2025-
dc.identifier.issn1936-0851-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/39176-
dc.description.abstractPeriodontal disease results from an imbalance between bacterial complexes and the immune system. However, periodontal disease diagnosis is limited by its time-consuming nature, long processing time, and high costs. In this study, we suggest an ultrafast, highly sensitive, and multitargeted plasmonic photothermal-based digital polymerase chain reaction (dPCR) method using a novel plasmonic photothermal-based dPCR chip combined with photothermal materials and organic interfacial chemicals for periodontal disease diagnosis. This platform can detect biofilm-forming bacteria (Streptococcus mutans), red complex bacteria (Porphyromonas gingivalis), and orange complex bacteria (Campylobacter rectus and Prevotella nigrescens). The ultrafast plasmonic photothermal-based dPCR technique amplified multiple target genes over 45 cycles within 14 min, and a fluorescence scanning system measured the fluorescence intensity within 9 min. The sensitivity of detection of standard bacteria and artificial saliva containing bacteria showed a sensitivity of 101 copies/μL. Furthermore, multiplex PCR was performed with a plasmonic photothermal-based dPCR device to confirm the possibility of multiplex PCR of bacterial mixtures containing four species. This plasmonic photothermal-based dPCR platform can be utilized as a point-of-care molecular diagnostic device for the ultrafast diagnosis of diseases in real-time in various fields.-
dc.publisherAmer Chem Soc-
dc.titleMultiplexed ultrafast photothermal digital polymerase chain reaction based on oligo(phenylene-ethynylene)-
dc.title.alternativeMultiplexed ultrafast photothermal digital polymerase chain reaction based on oligo(phenylene-ethynylene)-
dc.typeArticle-
dc.citation.titleACS Nano-
dc.citation.number30-
dc.citation.endPage27293-
dc.citation.startPage27280-
dc.citation.volume19-
dc.contributor.affiliatedAuthorKyong-Cheol Ko-
dc.contributor.alternativeName김경지-
dc.contributor.alternativeName김경호-
dc.contributor.alternativeName이병진-
dc.contributor.alternativeName한문정-
dc.contributor.alternativeName노승희-
dc.contributor.alternativeName홍석영-
dc.contributor.alternativeName김형교-
dc.contributor.alternativeName박선주-
dc.contributor.alternativeName윤완수-
dc.contributor.alternativeName박유민-
dc.contributor.alternativeName이경G-
dc.contributor.alternativeName고경철-
dc.contributor.alternativeName권오석-
dc.identifier.bibliographicCitationACS Nano, vol. 19, no. 30, pp. 27280-27293-
dc.identifier.doi10.1021/acsnano.5c04674-
dc.subject.keywordPeriodontitis diagnostics-
dc.subject.keywordUltrafast digital polymerase chain reaction, Plasmonic photothermal-based digital polymerase chain reaction-
dc.subject.keywordMultiplex polymerase chain reaction-
dc.subject.keywordOligo(phenylene-ethynylene)-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Korea Preclinical Evaluation Center > 1. Journal Articles
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