Droplet coalescence plays an important role in droplet-based microfluidics. This letter reports the phenomenon of thermocoalescence of two droplets in a chamber with an microheater. An integrated resistive sensor allows the measurement of heating temperature. The merging process was investigated at different flow rates. Experimental results showed that the droplet slows down at increasing temperature and eventually merges with the subsequent droplet. Coalescence occurs at a critical heating temperature. The letter discusses the relationship between droplet velocity, merging temperature and flow rates.
A microfluidic platform designed for point-of-care PCR-based nucleic acid diagnostics is described. Compared to established microfluidic PCR technologies, the system is unique in its ability to achieve exceptionally rapid PCR amplification in a low cost thermoplastic format, together with high temperature accuracy enabling effective validation of reaction product by high resolution melt analysis performed in the same chamber as PCR. In addition, the system employs capillary pumping for automated loading of sample into the reaction chamber, combined with an integrated hydrophilic valve for precise self-metering of sample volumes into the device. Using the microfluidic system to target a mutation in the G6PC gene, efficient PCR from human genomic DNA template is achieved with cycle times as low as 14 s, full amplification in 8.5 min, and final melt analysis accurately identifying the desired amplicon.
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