molecule & protein detection |
various electrode materials integrated into microchannel; various measurement and functionalities; easy operation in all environments |
fabrication complexity with increased number of embedded sensors, large fabrication error width in paper channel |
[40, 59, 61, 128, 129] |
cell deposition & simulation |
at the resolution of individual cells, the possible molecular interactions between cells, 3D concentration of gradients, precise control of fluids, reduced reagent/sample consumption, robust and automated procedure |
rather large fluidic channels, discrepancy between the printed and designed channel height |
[19, 63–67] |
bacterial communities |
multiple population, no external force required, little physical damage to cells |
hard to predict and control the flow behavior in a channel with varying curvatures, small bacterial concentration in the detection |
[68–70, 130] |
3D tissue constructs |
precise control over various cellular microenvironment, easy formation of desired structures, high throughput, reproducible, multi-layer structures |
trade-off between cell density of bioink and nozzle size |
[51, 74, 78–82, 85–88, 90, 91] |
organ-on-a-chip |
accurate position of various tissue samples |
throughput is limited by large components with intricate geometries |
[15, 17, 92, 118, 131] |
organ conformal biopsy |
rich diagnostic information, continuous monitoring, direct coupling |
unknown long-term effects for human |
[94] |
Milli- & micro-fluidic reactionware |
rapid production and design optimization, quick and versatile material synthesis, high temporal stability |
low output volume, inability at high pressure and temperature |
[62, 95–97] |