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] |