Thermal cycling characteristics of a 3D-printed serpentine microchannel for DNA amplification by polymerase chain reaction

•3D-printed thermal cycling device is experimentally studied.•The dimensions of the device are 3×4cm with 27 thermal cycles.•Thermal cycling efficiency is evaluated by the produced temperature zones.•3D-printing technology is feasible to microscale thermal cycler. A polymerase chain reaction (PCR) d...

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Veröffentlicht in:Sensors and actuators. A. Physical. 2017-12, Vol.268, p.183-187
Hauptverfasser: Park, Jaehyun, Park, Heesung
Format: Artikel
Sprache:eng
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Zusammenfassung:•3D-printed thermal cycling device is experimentally studied.•The dimensions of the device are 3×4cm with 27 thermal cycles.•Thermal cycling efficiency is evaluated by the produced temperature zones.•3D-printing technology is feasible to microscale thermal cycler. A polymerase chain reaction (PCR) device with integrated heaters for DNA amplification is proposed by using 3D-printing technology, which has the advantages of fast prototyping, design flexibility, and low cost. The thermal characteristics of the 3D-printed device for PCR are reported for the first time. The overall dimensions of the PCR device are 30mm×40mm where a serpentine microchannel is created to implement 27 thermal cycles. The serpentine microchannel of 260μm in depth, 450μm in width and 1470mm in length has been designed to inspect shape conformity and temperature variations. Thermal cycling experiments has showed that three temperature zones for denaturation (90–95°C), annealing (55–65°C) and extension (70–77°C) were successfully produced for DNA amplification. The thermal cycling efficiency ranges 67.4% to 47.8% when the flow rate is changed from 5μL/min to 10μL/min. The study demonstrates the feasibility of a low-cost 3D-printed PCR device that enables DNA amplification by thermal cycling. This paper concludes that 3D-printing technology can be applied for bio-microfluidic devices that require precise temperature control.
ISSN:0924-4247
1873-3069
DOI:10.1016/j.sna.2017.10.044