Transparent ultrasound chip improves cell stimulation and imaging
Ultrasound scans — best known for monitoring pregnancies or imaging organs — can also be used to stimulate cells and direct cell function. A team of Penn State researchers has developed an easier, more effective way to harness the technology for biomedical applications.
The team created a transparent, biocompatible ultrasound transducer chip that resembles a microscope glass slide and can be inserted into any optical microscope for easy viewing. Cells can be cultured and stimulated directly on top of the transducer chip and the cells’ resulting changes can be imaged with optical microscopy techniques.
Published in the Royal Society of Chemistry’s journal Lab on a Chip, the paper was selected as the cover article for the December 2021 issue. Future applications of the technology could impact stem cell, cancer and neuroscience research.
“In the conventional ultrasound stimulation experiments, a cell culture dish is placed in a water bath, and a bulky ultrasound transducer directs the ultrasound waves to the cells through the water medium,” said Sri-Rajasekhar “Raj” Kothapalli, principal investigator and assistant professor of biomedical engineering at Penn State. “This was a complex setup that didn’t provide reproducible results: The results that one group saw another did not, even while using the same parameters, because there are several things that could affect the cells’ survival and stimulation while they are in water, as well as how we visualize them.”
Kothapalli and his collaborators miniaturized the ultrasound stimulation setup by creating a transparent transducer platform made of a piezoelectric lithium niobate material. Piezoelectric materials generate mechanical energy when electric voltage is applied. The chip’s biocompatible surface allows the cells to be cultured directly on the transducer and used for repeated stimulation experiments over several weeks.
When connected to a power supply, the transducer emits ultrasound waves, which pulse the cells and trigger ion influx and outflux. More