Table 4.
Summary of microfluidic devices used to recreate the micro and nano spatial cues of the cell microenvironment.
| Application | Polymer | Outcome | Ref |
|---|---|---|---|
| Create a microfabrication platform to study adult NSC fate | SU-8 photoresist material coated with poly-ornithine and laminin, placed on oxygen plasma treated glass coverslips | An array of microwells with dimensions that ranged from 20 to 500 µm in diameter and 10–500 µm in height. | [137] |
| Study the effects of 3D microenvironment for NSCs on self-renewal and differentiation | PDMS surface coated with COL I fabricated with a SU-8 pattern master. A COL I hydrogel was used as a cell carrier | 3D collagen-coated microchannels of 140–160 μm height. | [138] |
| New fabrication approach to recreate stem cell niches using hydrogel engineering with droplet microfluidic technology | PDMS microfluidic bonded to glass coverslips using oxygen plasma. Chips were loaded with functionalized PEG hydrogels. | Microchannels array of 100 μm deep with three different channel widths of 100, 200, and 300 μm. | [139] |
| Generate a high-throughput platform to study the stem cell microenvironment with a tunable ratio of encapsulated species. | Cell-laden agarose microgels loaded into a functionalized PDMS surface. | An array of micro agarose gels of 70 to 110 µm. | [140] |
| Build functional networks that can be modified during the experiment to manipulate hMSC behavior in situ. | PDMS mount to cast crosslinked PED hydrogels | Artificial blood-vessel microfluidic network within cell-containing hydrogels. Channel diameter can be controlled in situ. | [141] |
| Create a two-layer microfluidic system to culture 3D multi-cell type spheroids to study cancer stem cell microenvironment. | PDMS device separated by a polycarbonate membrane and treated with 1% w/v Pluronic F108 | A microfluidic system with a lower channel of 100 μm H and 2 mm in W, and a central microchannel of 200 μm H and 50 μm in W. | [142] |