To develop a microfluidic platform that facilitates co-culture and focal irradiation within a closed environment.
Utilized a microfluidic system for co-culture of cell types.
Implemented unidirectional flow to maintain microenvironment integrity.
Applied focal irradiation to specific areas of the culture.
Demonstrated effective intercellular communication within the microphysiological system.
Showed robustness in maintaining controlled microenvironments for cell analysis.
Abstract
A microfluidic platform that enables co-culture and focal irradiation under closed microenvironments, providing a robust approach for analyzing intercellular communication.