Integration of plasmonic heating and on-chip temperature sensor for nucleic acid amplification assays

被引:7
|
作者
Monshat, Hosein [1 ]
Wu, Zuowei [2 ]
Pang, Jinji [2 ]
Zhang, Qijing [2 ]
Lu, Meng [1 ,3 ]
机构
[1] Iowa State Univ, Dept Mech Engn, Black Engn, Ames, IA USA
[2] Iowa State Univ, Dept Vet Microbiol & Prevent Med, Ames, IA USA
[3] Iowa State Univ, Dept Elect & Comp Engn, 2128 Coover Hall, Ames, IA 50011 USA
基金
美国国家科学基金会; 美国食品与农业研究所;
关键词
antibiotic resistance detection; nucleic acid-based diagnostics; photothermal effect; polymer chain reaction; thermocycler; thermoplasmonics; POLYMERASE-CHAIN-REACTION;
D O I
10.1002/jbio.202000060
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nucleic acid tests have been widely used for diagnosis of diseases by detecting the relevant genetic markers that are usually amplified using polymerase chain reaction (PCR). This work reports the use of a plasmonic device as an efficient and low-cost PCR thermocycler to facilitate nucleic acid-based diagnosis. The thermoplasmonic device, consisting of a one-dimensional metal grating, exploited the strong light absorption of plasmonic resonance modes to heat up PCR reagents using a near-infrared laser source. The plasmonic device also integrated a thin-film thermocouple on the metal grating to monitor the sample temperature. The plasmonic thermocycler is capable of performing a PCR amplification cycle in ~2.5 minutes. We successfully demonstrated the multiplex and real-time PCR amplifications of the antibiotic resistance genes using the genomic DNAs extracted fromAcinetobacter baumannii,Klebsiella pneumonia,Escherichia coliandCampylobacter.
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页数:9
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