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A microphysiological system (MPS), also known as an organ-on-a-chip, is a 3D organ construct using human cells that help reveal how organs respond to drugs and environmental stimuli.

Now, Tohoku University researchers have developed a new analytical method that visualizes cell functions in MPS using scanning probe microscopy (SPM).

SPM differs from optical microscopy since it employs fine probe scanning over a sample surface and then exploits the local interactions between the probe and the surface. The biggest advantage of SPM over conventional microscopy is that physical and chemical conditions can be acquired rapidly and as a high-resolution image.

In this study, SPMs evaluated a vascular model (vasculature-on-a-chip) by scanning electrochemical microscopy (SECM) and scanning ion conductance microscopy (SICM). Using these SPMs, the researchers quantified the permeability and topographical information of the vasculature-on-a-chip.

MPS shows potential to recapitulate the physiology and functions of their counterparts in the human body. Most research on this topic has focused on the construction of biomimetic organ models. Today, there is an increasing interest in developing sensing systems for MPS."

Yuji Nashimoto, Study First Author, Tohoku University

Some have touted electrochemical sensors to monitor MPS. However, actos juridicos documentados comunidad valenciana vivienda habitual most electrochemical sensors cannot acquire the spatial information of cell functions in MPS because they have only one sensor per one analyte. In contrast, SPM provides spatial information about cell functions rapidly.

"Our research group has developed various electrochemical imaging tools, SPMs and electrochemical arrays," explained corresponding author Hitoshi Shiku.

"These devices will help usher in next-generation sensors in MPS."

Source:

Tohoku University

Journal reference:

Nashimoto, Y., et al. (2021) Topography and Permeability Analyses of Vasculature-on-a-Chip Using Scanning Probe Microscopies. Advanced Healthcare Materials. doi.org/10.1002/adhm.202101186.

Posted in: Cell Biology | Histology & Microscopy

Tags: Analyte, Cell, CHIP, Drugs, Imaging, Ion, Microscopy, Physiology, Research, Scanning Probe Microscopy, Vascular, Vasculature

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