The organ-on-e-chip approach will help develop and assess the efficacy of drugs for disease treatment — perhaps even enabling researchers to screen for drugs and toxins directly on a human-like tissue, rather than testing on animal tissue. The platform will be used to shed light on the connection between the heart’s electrical signals and disease, such as arrhythmias. The research, published in Science Advances, allows the researchers to investigate processes in cultured cells that currently are not accessible, such as tissue development and cell maturation.
“For decades, electrophysiology was done using cells and cultures on two-dimensional surfaces, such as culture dishes,” said Tzahi Cohen-Karni, an associate professor of biomedical engineeringand materials science and engineering. “We are trying to circumvent the challenge of reading the heart’s electrical patterns in 3D by developing a way to shrink-wrap sensors around heart cells and extracting electrophysiological information from this tissue.”
The “organ-on-e-chip” platform starts out as a small, flat rectangle, not unlike a microscale slap bracelet. A slap bracelet starts out as a rigid, ruler-like structure, but when you release the tension it quickly coils up to band around the wrist.
The organ-on-e-chip starts out similarly. The researchers pin an array of sensors made of either metallic electrodes or graphene sensors to the chip’s surface, then etch off a bottom layer of germanium, which is known as the “sacrificial layer.” Once this sacrificial layer is removed, the biosensor array is released from its hold and rolls up from the surface in a barrel-shaped structure.
The researchers tested the platform on cardiac spheroids, or elongated organoids made of heart cells. These 3D heart spheroids are about the width of two to three human hairs. Coiling the platform over the spheroid allows the researchers to collect electrical signal readings with high precision.
“Essentially, we have created 3D self-rolling biosensor arrays for exploring the electrophysiology of induced pluripotent stem cell derived cardiomyocytes,” said Anna Kalmykov, the lead author of the study and a Ph.D. student in biomedical engineering. “This platform could be used to do research into cardiac tissue regeneration and maturation that potentially can be used to treat damaged tissue after a heart attack, for example, or developing new drugs to treat disease.”
Through collaboration with the labs of Adam Feinberg and Jimmy Hsia, the researchers were able to design a proof of concept and test them on 3D micro-mold formed cardiomyocyte spheroids.
“Mechanics analysis of the roll-up process enables us to precisely control the shape of the sensors to ensure conforming contact between the sensors and the cardiac tissue,” said Hsia, professor and dean of the Graduate College of NTU Singapore and former CMU faculty member. “The technique also automatically adjusts the level of the delicate ‘touch’ between the sensors and the tissue such that high quality electric signals are measured without changing in the physiological conditions of the tissue due to external pressure.”
“The whole idea is to take methods that are traditionally done in planar geometry and do them in three dimensions,” Cohen-Karni said. “Our organs are 3D in nature. For many years, electrophysiology was done using just cells cultured on a 2D tissue culture dish. But now, these amazing electrophysiology techniques can be applied to 3D structures.”
This work was made possible by support from the National Science Foundation CAREER Award and the Office of Naval Research Young Investigator Program. Other authors on this paper include CMU BME/MSE Professor Adam Feinberg; CMU BME/MSE researchers Jacqueline Bliley, Daniel Shiwarski, Joshua Tashman, Sahil Rastogi, Shivani Shukla, and Elnatan Mataev; NTU’s Jimmy Hsia and Changjin Huang; and University of Illinois at Urbana-Champaign’s Arif Abdullah.