ERROR 1
ERROR 1
ERROR 2
ERROR 2
ERROR 2
ERROR 2
ERROR 2
Password and Confirm password must match.
If you have an ACS member number, please enter it here so we can link this account to your membership. (optional)
ERROR 2
ACS values your privacy. By submitting your information, you are gaining access to C&EN and subscribing to our weekly newsletter. We use the information you provide to make your reading experience better, and we will never sell your data to third party members.
A new array of microfabricated silicon cantilevers gives researchers a way to track the growth of individual adherent cells.
Common methods for characterizing single cells, such as flow cytometry, require that cells be suspended in a solution. But many so-called adherent cells, such as fibroblast and epithelial cells, must be attached to a surface to grow.
Rashid Bashir, a professor of electrical engineering, computer engineering, and bioengineering at the University of Illinois, Urbana-Champaign, and coworkers at Purdue University, Harvard Medical School, and Ohio State University describe arrays of silicon cantilevers that can determine the mass of individual adherent cells without detaching them from the surface (Lab Chip, DOI: 10.1039/b803601b). The researchers calculate cell mass by measuring cell-growth-induced changes in each cantilever's resonance frequency, which is inversely proportional to the square root of its mass. Cells on the cantilever surface change the device's effective mass and thus its resonance frequency.
The researchers cultured cancer cells on the cantilevers and calculated the cells' mass from resonance frequency shifts of the cantilevers. The cells were smaller than normal, possibly because they were constrained by the size of the cantilevers. Because the cells don't need to be detached from the surface, the technology can be used for time-course studies of individual cells.
Join the conversation
Contact the reporter
Submit a Letter to the Editor for publication
Engage with us on Twitter