Hybrid Digital-Droplet Microfluidic Chip for Applications in Droplet Digital Nucleic Acid Amplification: Design, Fabrication and Characterization

• Published in: Sensors (Basel, Switzerland) Vol. 23; no. 10; p. 4927
• Main Authors: Coelho, Beatriz J, Neto, Joana P, Sieira, Bárbara, Moura, André T, Fortunato, Elvira, Martins, Rodrigo, Baptista, Pedro V, Igreja, Rui, Águas, Hugo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 20.05.2023; MDPI
• Subjects: Acids; Biological Assay; Continuous flow; digital microfluidics; droplet microfluidics; Droplets; Electrodes; flow focusing; Glass substrates; Lab-On-A-Chip Devices; Microfluidics; negative pressure; Nucleic Acids; Reagents; Reynolds number; Severe acute respiratory syndrome coronavirus 2; Technology; Germany; droplet microfluidics; digital microfluidics; negative pressure; flow focusing
• ISSN: 1424-8220; 1424-8220
• DOI: 10.3390/s23104927

Microfluidic-based platforms have become a hallmark for chemical and biological assays, empowering micro- and nano-reaction vessels. The fusion of microfluidic technologies (digital microfluidics, continuous-flow microfluidics, and droplet microfluidics, just to name a few) presents great potential for overcoming the inherent limitations of each approach, while also elevating their respective strengths. This work exploits the combination of digital microfluidics (DMF) and droplet microfluidics (DrMF) on a single substrate, where DMF enables droplet mixing and further acts as a controlled liquid supplier for a high-throughput nano-liter droplet generator. Droplet generation is performed at a flow-focusing region, operating on dual pressure: negative pressure applied to the aqueous phase and positive pressure applied to the oil phase. We evaluate the droplets produced with our hybrid DMF-DrMF devices in terms of droplet volume, speed, and production frequency and further compare them with standalone DrMF devices. Both types of devices enable customizable droplet production (various volumes and circulation speeds), yet hybrid DMF-DrMF devices yield more controlled droplet production while achieving throughputs that are similar to standalone DrMF devices. These hybrid devices enable the production of up to four droplets per second, which reach a maximum circulation speed close to 1540 µm/s and volumes as low as 0.5 nL.