Miniaturising disease diagnosis tool
30 March 2012
South Korean scientists have created a temperature cycle for the on-chip flow-through polymerase chain reaction (PCR) using a single heater.
PCR is used to make copies of a piece of DNA for genetic research, disease analysis and diagnosis. It consists of four main steps - initialisation; denaturation (melting the DNA template to yield single-stranded DNA); annealing primers to the single-stranded DNA template; and extension, in which the DNA polymerase synthesises a new DNA strand complementary to the DNA template.
On-chip flow-through PCR typically has a short reaction time due to rapid thermal equilibrium allowing quick temperature transitions; however, it normally requires several separate heating blocks to create the different temperatures. Reducing the number of heaters will help make the whole system smaller and more portable. 'Analysing samples on site could help prevent degradation and contamination,' explains Nae Yoon Lee from Gachon University, South Korea, who led the research.
The team combined the low thermal conductivity of the chip material (polydimethylsiloxane) with a qiandu shape (right triangular prism) to create a height dependent temperature gradient using a single heater. Placing the heater at the base of the qiandu creates a natural temperature gradient on the slanted face. The bottom of the slanted plane is closer the heater and therefore hotter than the top.
A height-dependent linear temperature gradient established on the inclined surface of a 3D qiandu (right triangular prism)-shaped PDMS microdevice enables flow-through PCR employing a single heater
Liquid flowing through micro-channels on the face of the qiandu changes temperature as it moves from the bottom to the top and back to the bottom again, creating a natural temperature cycle. Lee and the team showed that using a single continuous micro-channel that repeatedly cycles up and down the face of the qiandu can create the different temperatures required for the denaturation, annealing and extension steps in the PCR.
Lee explains that a practical micro total analysis system for disease analysis or diagnosis requires more than just the micro-channels and heaters. To make it easily transportable will require 'miniaturising the accessories, such as the pump and detection systems', however, the team hopes that these components will be miniaturised soon.
Tom Brown, an expert in nucleic acid chemistry at the University of Southampton, UK, says that a portable PCR device could find widespread use. 'Portable PCR devices could be used in important applications in human and veterinary medicine for point of care analysis, and in forensic science for identification,' he says.
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W Wu, K T L Trinh and N Y Lee, Analyst, 2012, DOI: 10.1039/c2an35077g
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