TABLE I.
Types of vascularization methods.
| Vascularization method | Benefits | Limitations |
|---|---|---|
| Fluid flow through constructed, endothelial cell-lined channel that connects to the culture chamber | • Relatively simple and easy to implement • Allows for modeling of flow effects • Allows for greater control of perfusion medium |
• Does not recapitulate complex, branched geometries present in vasculature in vivo |
| Self-assembled microvasculature formed by endothelial cells under static conditions | • Self-assembly and de novo vessel formation recreates processes that occur in vivo
• Greater likelihood of faithfully modeling in vivo vasculature |
• Lacks effects of fluid flow that influence endothelial cell orientation and morphology in vivo
• May be difficult to control flow in certain chip formats |
| Artificial method to create a biomimetic network | • Allows greater degree of researcher control over the vascularized network • More complex geometries can be recapitulated • Greater resemblance to in vivo vasculature than flow through microfluidic channels |
• Vessel formation is not de novo and may not possess complete fidelity to in vivo vasculature • If synthetic material used is not sacrificial, its interactions with cells may influence results |
| Self-assembled microvasculature formed by endothelial cells under flow conditions | • Closest to recapitulating in vivo vasculature • Models flow effects and self-assembly ensures recapitulation of in vivo vessel formation processes |
• May be difficult to successfully implement • In multi-organ chips, it may be difficult to control perfusion of multiple media types |