• DocumentCode
    2207136
  • Title

    Design proposal for a microfluidic device for sprouting angiogenesis

  • Author

    Calt, M.A. ; Sempkowski, M.K. ; Lamba, R. ; Ahlawat, S. ; Anderson, C.

  • Author_Institution
    Coll. of New Jersey, Ewing, NJ, USA
  • fYear
    2012
  • fDate
    16-18 March 2012
  • Firstpage
    333
  • Lastpage
    334
  • Abstract
    Cancer growth and metastasis is dependent on angiogenesis, the development of new blood vessels. Endothelial cell proliferation and migration are critical cellular processes in the formation of new blood vessels. Many anticancer therapies are aimed at inhibiting angiogenesis, and there is a need for the development of in vitro models for studying these cellular processes. The goal of this project is to develop a microfluidic device for the purpose of observing cell migration in response to controlled mechanical and chemical stimuli. To represent physiological microvasculature, the system exhibits a central cell culture channel (1 mm diameter) and two parallel reservoir channels. A port system was also designed to drive fluid flow through the cell culture chamber with an external syringe pump and introduce chemotaxins or control conditions in the reservoirs. This will create an environment conducive to cell migration under the effects of fluid shear stresses. Computational fluid dynamics will be used to predict mechanical stresses inside the cell culture chamber and cell migration will be observed with inverted light microscopy. The successful implementation of our design will introduce a unique platform that models sprouting angiogenesis and allows for the independent control of fluid shear stresses and chemical concentration gradients.
  • Keywords
    bioMEMS; biological fluid dynamics; biomedical equipment; blood vessels; cancer; cell motility; computational fluid dynamics; microchannel flow; optical microscopy; shear flow; angiogenesis; anticancer therapy; blood vessels; cancer growth; cell culture chamber; cell culture channel; cellular process; chemical concentration gradients; chemical stimuli; chemotaxins; computational fluid dynamics; control conditions; endothelial cell migration; endothelial cell proliferation; external syringe pump; fluid flow; fluid shear stresses; in-vitro models; inverted light microscopy; mechanical stimuli; mechanical stress; microfluidic device; parallel reservoir channels; physiological microvasculature; port system; Chemicals; Computational fluid dynamics; Microfluidics; Microscopy; Reservoirs; Stress; Tumors;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioengineering Conference (NEBEC), 2012 38th Annual Northeast
  • Conference_Location
    Philadelphia, PA
  • ISSN
    2160-7001
  • Print_ISBN
    978-1-4673-1141-0
  • Type

    conf

  • DOI
    10.1109/NEBC.2012.6207100
  • Filename
    6207100