Title :
Microfluidic cell culture array for on-chip cell biology
Author :
Lee, P.J. ; Hung, P.J. ; Lee, L.P.
Author_Institution :
Dept. of Bioeng., California Univ., Berkeley, CA, USA
Abstract :
An arrayed microfluidic platform was developed for cell biology applications. Using soft lithography methods, individual cell culture units were fabricated with a diameter from 50-500 μm. The channel height aspect ratio modulation (CHARM) design allowed fine control of fluidic flow through the array, enabling uniform cell loading, reduced shear stress, and decoupling of fluid transport from cell growth. A variety of adherent mammalian tissue culture cell lines were successfully cultured in the array with continuous perfusion of medium for over 2 weeks. Individual culture units were multiplexed in 2 dimensions to create 6×6 and 8×8 arrays, allowing row and column addressing to provide a unique culture environment in each microchamber. Demonstrated functionalities for cell biology research included repeated cell passaging in a fully enclosed microenvironment, fluorescent cell analysis (live and fixed), on-chip protein transfection, and multiplexed long-term "flow-cell" microscopy.
Keywords :
biological techniques; biomechanics; biotechnology; cellular biophysics; microfluidics; molecular biophysics; proteins; soft lithography; 2 weeks; 50 to 500 micron; adherent mammalian tissue culture cell line; cell growth; channel height aspect ratio modulation design; enclosed microenvironment; fluid transport decoupling; fluidic flow control; fluorescent cell analysis; individual cell culture unit fabrication; microchamber; microfluidic cell culture array; multiplexed long-term flow-cell microscopy; on-chip cell biology; on-chip protein transfection; reduced shear stress; repeated cell passaging; soft lithography method; uniform cell loading; Biological cells; Biomedical engineering; Cells (biology); Fabrication; Fluid flow control; Immune system; Microfluidics; Numerical analysis; Soft lithography; Throughput;
Conference_Titel :
Microtechnology in Medicine and Biology, 2005. 3rd IEEE/EMBS Special Topic Conference on
Print_ISBN :
0-7803-8711-2
DOI :
10.1109/MMB.2005.1548481