A digital microfluidic system for loop-mediated isothermal amplification and sequence specific pathogen detection

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作者
Liang Wan
Tianlan Chen
Jie Gao
Cheng Dong
Ada Hang-Heng Wong
Yanwei Jia
Pui-In Mak
Chu-Xia Deng
Rui P. Martins
机构
[1] State-Key Laboratory of Analog and Mixed-Signal VLSI,Department of ECE
[2] University of Macau,undefined
[3] Faculty of Science and Technology,undefined
[4] University of Macau,undefined
[5] Cancer Centre,undefined
[6] Faculty of Health Sciences,undefined
[7] University of Macau,undefined
[8] Instituto Superior Técnico,undefined
[9] Universidade de Lisboa,undefined
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摘要
A digital microfluidic (DMF) system has been developed for loop-mediated isothermal amplification (LAMP)-based pathogen nucleic acid detection using specific low melting temperature (Tm) Molecular Beacon DNA probes. A positive-temperature-coefficient heater with a temperature sensor for real-time thermal regulation was integrated into the control unit, which generated actuation signals for droplet manipulation. To enhance the specificity of the LAMP reaction, low-Tm Molecular Beacon probes were designed within the single-stranded loop structures on the LAMP reaction products. In the experiments, only 1 μL of LAMP reaction samples containing purified Trypanosoma brucei DNA were required, which represented over a 10x reduction of reagent consumption when comparing with the conventional off-chip LAMP. On-chip LAMP for unknown sample detection could be accomplished in 40 min with a detection limit of 10 copies/reaction. Also, we accomplished an on-chip melting curve analysis of the Molecular Beacon probe from 30 to 75 °C within 5 min, which was 3x faster than using a commercial qPCR machine. Discrimination of non-specific amplification and lower risk of aerosol contamination for on-chip LAMP also highlight the potential utilization of this system in clinical applications. The entire platform is open for further integration with sample preparation and fluorescence detection towards a total-micro-analysis system.
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