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Instrumented cardiac microphysiological devices via multimaterial three-dimensional printing.

Johan U LindTravis A BusbeeAlexander D ValentineFrancesco S PasqualiniHongyan YuanMoran YadidSung-Jin ParkArda KotikianAlexander P NesmithPatrick H CampbellJoost J VlassakJennifer A LewisKevin K Parker
Published in: Nature materials (2016)
Biomedical research has relied on animal studies and conventional cell cultures for decades. Recently, microphysiological systems (MPS), also known as organs-on-chips, that recapitulate the structure and function of native tissues in vitro, have emerged as a promising alternative. However, current MPS typically lack integrated sensors and their fabrication requires multi-step lithographic processes. Here, we introduce a facile route for fabricating a new class of instrumented cardiac microphysiological devices via multimaterial three-dimensional (3D) printing. Specifically, we designed six functional inks, based on piezo-resistive, high-conductance, and biocompatible soft materials that enable integration of soft strain gauge sensors within micro-architectures that guide the self-assembly of physio-mimetic laminar cardiac tissues. We validated that these embedded sensors provide non-invasive, electronic readouts of tissue contractile stresses inside cell incubator environments. We further applied these devices to study drug responses, as well as the contractile development of human stem cell-derived laminar cardiac tissues over four weeks.
Keyphrases
  • left ventricular
  • gene expression
  • low cost
  • single cell
  • skeletal muscle
  • cell therapy
  • endothelial cells
  • emergency department
  • stem cells
  • drug delivery
  • ionic liquid
  • ultrasound guided
  • gestational age
  • drug release