Potentiometric Multichannel Cytometer Microchip for High-throughput Microdispersion Analysis

초록

The parallelization of microfluidic cytometry is expected to lead to considerably enhanced throughput enabling point-of-care diagnosis. In this article, the development of a microfluidic potentiometric multichannel cytometer is presented. Parallelized microfluidic channels sharing a fluid path inevitably suffer from interchannel signal crosstalk that results from electrical coupling within the microfluidic channel network. By employing three planar electrodes within a single detection channel, we electrically decoupled each channel unit, thereby enabling parallel analysis by using a single cytometer microchip with multiple microfluidic channels. The triple-electrode configuration is validated by analyzing the size and concentration of polystyrene microbeads (diameters: 1.99, 2.58, 3, and 3.68 mu m; concentration range: similar to 2 x 10(5) mL(-1) to similar to 1 x 10(7) mL(-1)) and bacterial rnicrodispersion samples (Bacillus subtilis, concentration range: similar to 4 x 10(5) CFU mL(-1) to similar to 3 x 10(6) CFU mL(-1)). Crosstalk-free parallelized analysis is then demonstrated using a 16-channel potentiometric cytometer (maximum cross-correlation coefficients vertical bar r vertical bar: < 0.13 in all channel combinations). A detection throughput of similar to 48 000 s(-1) was achieved; the throughout can be easily increased with the degree of parallelism of a single microchip without additional technical complexities. Therefore, this methodology should enable high-throughput and low-cost cytometry.

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