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基于聚对苯撑乙炔的多重超快光热数字聚合酶链反应

Multiplexed Ultrafast Photothermal Digital Polymerase Chain Reaction Based on Oligo(Phenylene-Ethynylene).

作者信息

Kim Gyeong-Ji, Kim Kyung Ho, Lee Byoungjin, Han Munjung, Rho Seunghee, Hong Seok Young, Kim Hyung Kyo, Park Seon Joo, Yun Wan Soo, Park Yoo Min, Lee Kyoung G, Ko Kyong-Cheol, Kwon Oh Seok

机构信息

SKKU Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon-si, Gyeonggi-do 16419, Republic of Korea.

Denomics Co., Ltd., Laboratory of life science, 5, Digital-ro 26-gil, Guro-gu, Seoul 08389, Republic of Korea.

出版信息

ACS Nano. 2025 Aug 5;19(30):27280-27293. doi: 10.1021/acsnano.5c04674. Epub 2025 Jul 24.

Abstract

Periodontal 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 (), red complex bacteria (), and orange complex bacteria ( and ). 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 10 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.

摘要

牙周疾病源于细菌复合体与免疫系统之间的失衡。然而,牙周疾病的诊断受到其耗时、处理时间长和成本高的限制。在本研究中,我们提出了一种基于等离子体光热的超快速、高灵敏度和多靶点数字聚合酶链反应(dPCR)方法,该方法使用一种新型的基于等离子体光热的dPCR芯片,结合光热材料和有机界面化学物质用于牙周疾病诊断。该平台可检测形成生物膜的细菌()、红色复合体细菌()和橙色复合体细菌(和)。基于等离子体光热的超快速dPCR技术在14分钟内45个循环内扩增多个靶基因,荧光扫描系统在9分钟内测量荧光强度。标准细菌和含细菌人工唾液的检测灵敏度为10拷贝/μL。此外,使用基于等离子体光热的dPCR装置进行多重PCR,以确认包含四种细菌的混合物进行多重PCR的可能性。这种基于等离子体光热的dPCR平台可作为即时分子诊断设备,用于在各个领域实时超快速诊断疾病。

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