2009
DOI: 10.1039/b817288a
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Petri dish PCR: laser-heated reactions in nanoliter droplet arrays

Abstract: We report high-speed real-time PCR performed on an unmodified disposable polystyrene Petri dish. The reaction cycle relies solely on an infrared laser for heating; no conventional heater is required. Nanoliter droplets of PCR mixture as water-in-oil emulsions printed in an array format served as individual PCR microreactors. A simple contact printing technique was developed to generate a large array of uniform sized nanoliter droplets using disposable pipette tips. Printed droplets showed variation of less tha… Show more

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Cited by 75 publications
(61 citation statements)
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“…33,36 In addition, such data are critical to applications in which the droplet temperatures control physical processes other than evaporation, such as voltage-induced modulation of droplet temperatures for biosensing, 37 control of reaction rates in droplet microfluidics, 38,39 and temperature modulation to denature DNA for polymerase chain reactions. 40,41 The methodology is also broadly applicable for characterizing the temperature of curved interfaces.…”
Section: -2mentioning
confidence: 99%
“…33,36 In addition, such data are critical to applications in which the droplet temperatures control physical processes other than evaporation, such as voltage-induced modulation of droplet temperatures for biosensing, 37 control of reaction rates in droplet microfluidics, 38,39 and temperature modulation to denature DNA for polymerase chain reactions. 40,41 The methodology is also broadly applicable for characterizing the temperature of curved interfaces.…”
Section: -2mentioning
confidence: 99%
“…In addition, laser-induced heating has also been utilized to assist biological process [25], which benefits from a small heating region controlled by laser spot. The precise temperature detection and calibration rely on microsensor [26,27] or optical imaging technique [28]. Although many studies have focused on the laser-induced heating effect, the effect occurring in the solid and fluid flow, a more complicated problem, was found in our previous work.…”
Section: Introductionmentioning
confidence: 95%
“…Because fast/ultrafast PCR is highly desirable for applications such as timely diagnosis of infectious diseases, cardiac diseases, cancer, neurological disorder diseases, and rapid biowarfare and pathogen identification at the point-of-care (POC) level, many academic and industrial groups have worked on improving PCR systems, [9][10][11][12][13][14][15] One commercial PCR system (LightCycler H 2.0, Roche Diagnostics USA, Indianapolis, IN, USA) using air heating/cooling and capillary tubes can perform 30 thermal cycles in 10-60 min, depending on sample volume. 10 However, this system is not suitable for POC testing due to its high power consumption (800 W maximum) and heavy weight (approximately 22 kg).…”
Section: Introductionmentioning
confidence: 99%
“…Another approach includes infrared-mediated non-contact selective heating of water droplets (nanoliter sample volume) for ultrafast thermal cycling using an infrared laser, which harnesses the strong absorbance of water at wavelengths over 1000 nm. 14,15 However, droplet formation from the PCR mixture is a precise process prone to human error, which is a drawback for POC testing.…”
Section: Introductionmentioning
confidence: 99%