Microphysiological systems and low-cost microfluidic platform with analytics

Stem Cell Res Ther. 2013;4 Suppl 1(Suppl 1):S9. doi: 10.1186/scrt370. Epub 2013 Dec 20.

Abstract

A multiorgan, functional, human in vitro assay system or 'Body-on-a-Chip' would be of tremendous benefit to the drug discovery and toxicology industries, as well as providing a more biologically accurate model for the study of disease as well as applied and basic biological research. Here, we describe the advances our team has made towards this goal, as well as the most pertinent issues facing further development of these systems. Description is given of individual organ models with appropriate cellular functionality, and our efforts to produce human iterations of each using primary and stem cell sources for eventual incorporation into this system. Advancement of the 'Body-on-a-Chip' field is predicated on the availability of abundant sources of human cells, capable of full differentiation and maturation to adult phenotypes, for which researchers are largely dependent on stem cells. Although this level of maturation is not yet achievable in all cell types, the work of our group highlights the high level of functionality that can be achieved using current technology, for a wide variety of cell types. As availability of functional human cell types for in vitro culture increases, the potential to produce a multiorgan in vitro system capable of accurately reproducing acute and chronic human responses to chemical and pathological challenge in real time will also increase.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Blood-Brain Barrier / metabolism
  • Cell Survival / drug effects
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Fluoroquinolones / chemistry
  • Fluoroquinolones / toxicity
  • Gases / metabolism
  • Heptanol / chemistry
  • Heptanol / toxicity
  • Humans
  • Lung / cytology
  • Microfluidic Analytical Techniques / instrumentation
  • Microfluidic Analytical Techniques / methods*
  • Models, Biological
  • Muscle, Skeletal / cytology
  • Myocardium / cytology

Substances

  • Fluoroquinolones
  • Gases
  • Heptanol
  • sparfloxacin