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Updated: Aug 5, 2026

Microfluidic Chip Fabrication and Method to Detect Influenza
Published on: March 26, 2013
Capillary-Driven Microfluidic Electrical Screening of Influenza H3N2-Infected A549 Cells Using AgNP-Decorated
Zhaochi Chen1, Minh-Quang Tran2
1Graduate Institute of Biomedical Optomechatronics, Taipei Medical University, Taipei 230, Taiwan.
Abstract:
A capillary-driven microfluidic electrical screening platform was developed using silver nanoparticle (AgNP)-decorated laser-patterned villous microstructures on a glass substrate for the analysis of H3N2-infected A549 cells. The device integrated nanosecond laser patterning, AgNP conductive thin-film formation, passive capillary transport, and direct electrical readout within a single microfluidic sensing structure. Villous-like arrays were fabricated using a 1064 nm IR pulsed laser at a fluence of 4.35 J/cm2, with a repetition rate of 300 kHz, pulse overlap of 96.7% and scanning speed of 500 mm/s. The fabricated structures exhibited a diameter of 60 μm, height of 80 μm and interpillar pitches ranging from 30 to 90 μm. After AgNP deposition, the surface showed a dominant Ag content of 59.2%, confirming successful formation of conductive microstructured electrodes. The 30 μm pitch structure produced the highest current response of 22 μA at 1 V and the highest ΔInorm of 0.053 after introduction of H3N2-infected A549 samples. Wettability and capillary transport were tunable by pitch, with contact angles (CAs) decreasing from 140° to 30° and flow velocities decreasing from 0.1 mm/s to 0.03 mm/s. Formalin-fixed H3N2-infected A549 cells were electrically distinguished from non-infected A549 controls over 101-106 PFU/μL, with detectable responses down to 101 PFU/μL. These results demonstrate a label-free, self-driven, and fabrication-oriented microfluidic strategy for electrical screening of virus-associated cellular samples.

