A plasmonic gold nanofilm-based microfluidic chip for rapid and inexpensive droplet-based photonic PCR

Polymerase chain reaction (PCR) is a powerful tool for nucleic acid amplification and quantification. However, long thermocycling time is a major limitation of the commercial PCR devices in the point-of-care (POC). Herein, we have developed a rapid droplet-based photonic PCR (dpPCR) system, including a gold (Au) nanofilm-based microfluidic chip and a plasmonic photothermal cycler. The chip is fabricated by adding mineral oil to uncured polydimethylsiloxane (PDMS) to suppress droplet evaporation in PDMS microfluidic chips during PCR thermocycling. A PDMS to gold bonding technique using a double-sided adhesive tape is applied to enhance the bonding strength between the oil-added PDMS and the gold nanofilm. Moreover, the gold nanofilm excited by two light-emitting diodes (LEDs) from the top and bottom sides of the chip provides fast heating of the PCR sample to 230 degrees C within 100 s. Such a design enables 30 thermal cycles from 60 to 95 degrees C within 13 min with the average heating and cooling rates of 7.37 +/- 0.27 degrees C/s and 1.91 +/- 0.03 degrees C/s, respectively. The experimental results demonstrate successful PCR amplification of the alcohol oxidase (AOX) gene using the rapid plasmonic photothermal cycler and exhibit the great performance of the microfluidic chip for droplet-based PCR.

Automated summary

A rapid droplet-based photonic PCR system was developed using a gold nanofilm-based microfluidic chip and a plasmonic photothermal cycler, achieving fast thermal cycling and successful amplification of the AOX gene. The microfluidic chip demonstrated great performance in droplet-based PCR.