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
Link To Document :
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