Direct casting of polymer membranes into microfluidic devices

A. Peter Russo, Scott T. Retterer, Andrew J. Spence, Michael S. Isaacson, Lori A. Lepak, Michael G. Spencer, David L. Martin, Robert MacColl, James N. Turner

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Fully functional lab-on-a-chip devices for biological analyses require the capability for cell culture, separation, and purification, as well as analyses to be integrated on a single platform. To date, a great deal of research has been focused on analytical methods for the miniaturization of column-based separations. We have created a platform that provides the capability of including membrane separations as an intermediate stage in such devices. Our techniques adapt conventional silicon processing methods to the casting of membranes directly onto the silicon substrate through a wet inversion process. This process allows precise control of membrane thickness and pore size distribution based on the processing conditions. Using this methodology, we were able to fabricate devices that were found to be very robust with molecular weight cutoffs of approximately 350 Da as measured by solute flux in a dialysis mode of operation. These devices were also found to be suitable for cell culture, as evidenced by the high viability of fibroblasts grown within our device. On the basis of these results, a wide range of separations and coculture applications are possible.

Original languageEnglish
Pages (from-to)2515-2530
Number of pages16
JournalSeparation Science and Technology (Philadelphia)
Volume39
Issue number11
DOIs
StatePublished - 2004
Externally publishedYes

Funding

This work is supported by the STC Program of the National Science Foundation under Agreement No. ECS-9876771. This work was performed in part at the Cornell Nanofabrication Facility (a member of the National Nanofabrication Users Network), which is supported by the National Science Foundation under Grant ECS-9731293, its users, Cornell University, and Industrial Affiliates. The authors also acknowledge the assistance of the Biochemistry Core and the Electron Microscopy Core at the Wadsworth Center, which is supported by the National Science Foundation Grant DBI-0116551.

FundersFunder number
National Science FoundationECS-9731293
Cornell UniversityDBI-0116551

    Keywords

    • Biological analyses
    • Cell culture
    • Lab-on-a-chip
    • Microfluidic devices
    • Molecular separation
    • Polymer membranes

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