Tissue Engineering · 2005 · 341 citations · 9 references
EngineeringBioengineeringBiomedical EngineeringMicroelectromechanical SystemsMicrofabricationTissue EngineeringBiomaterials For Tissue EngineeringBiomedical MemsMicrofluidic Device FabricationMicrofluidic DevicesMicrofluidic SystemsMicrofluidicsMicromachining Of Silicon WafersMicrovascular Network FormationSiliconSilicon WafersSyringe PumpsTissue-engineered Blood VesselsVascular Tissue EngineeringVascularization Of Engineered Tissues
Vital organs rely on dense microvasculature to sustain cellular function, so tissue‑engineered organs require artificial capillary networks to perform properly. The study aims to develop endothelialized microvasculature that could be essential for engineering vital organs. Capillary patterns were etched onto silicon wafers using MEMS, then used as micromolds to bond patterned PGS films into perfusable networks driven at physiological flow rates. Microfabricated PGS capillary networks were endothelialized under flow, with parts of the lumens reaching confluence within 14 days of culture.
Vital organs maintain dense microvasculature to sustain the proper function of their cells. For tissue- engineered organs to function properly, artificial capillary networks must be developed. We have microfabricated capillary networks with a biodegradable and biocompatible elastomer, poly(glycerol sebacate) (PGS). We etched capillary patterns onto silicon wafers by standard microelectromechanical systems (MEMS) techniques. The resultant silicon wafers served as micromolds for the devices. We bond the patterned PGS film with a flat film to create capillary networks that were perfused with a syringe pump at a physiological flow rate. The devices were endothelialized under flow conditions, and part of the lumens reached confluence within 14 days of culture. This approach may lead to tissue-engineered microvasculature that is critical in vital organs engineering.
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