Biosensor for measuring hydrogen peroxide developed


Wednesday, 17 March, 2021

Biosensor for measuring hydrogen peroxide developed

Japanese researchers have successfully tested a sensor for measuring hydrogen peroxide concentrations near cell membranes. Described in the journal Biosensors and Bioelectronics, the sensor has the potential to become a tool for new cancer therapies.

Several processes in the human body are regulated by biochemical reactions involving hydrogen peroxide (H2O2). Although it can act as a ‘secondary messenger’, relaying or amplifying certain signals between cells, H2O2 is generally toxic because of its oxidant character. The latter means that it converts (oxidises) biochemical molecules like proteins and DNA. The oxidising property of H2O2 is of potential therapeutic relevance for cancer, though: deliberately causing tumour cells to increase their H2O2 concentration would be a way to destroy them.

In light of this, but also for monitoring pathologies associated with H2O2 overproduction, it is crucial to have a means to reliably quantify hydrogen peroxide concentrations in the extracellular environment. Leonardo Puppulin, from Kanazawa University’s Nano Life Science Institute (WPI-NanoLSI), and colleagues have now developed a sensor for measuring concentrations of H2O2 in the vicinity of cell membranes, with nanometre resolution.

The biosensor is based on a method called surface-enhanced Raman spectroscopy (SERS). The principle derives from Raman spectroscopy, in which differences between the incoming and the outgoing frequencies of laser light irradiated onto a sample are analysed. The spectrum obtained by plotting the signal strength as a function of frequency difference is characteristic for the sample, which can in principle be a single molecule. Typically the signal coming from one molecule is too weak to detect, but the effect can be enhanced when the molecule is absorbed on a rough metal surface.

The biosensor consists of a gold nanoparticle with organic molecules attached to it. The whole cluster is designed so that it anchors easily to the outside of a cell’s membrane, which is exactly where the hydrogen peroxide molecules to be detected are. As attachment molecules, the scientists used a compound called 4MPBE, known to have a strong Raman scattering response: when irradiated by a laser, the molecules consume some of the laser light’s energy.

By measuring the frequency change of the laser light, and plotting the signal strength as a function of this change, a unique spectrum is obtained — a signature of the 4MPBE molecules. When a 4MPBE molecule reacts with a H2O2 molecule, its Raman spectrum changes. Based on this principle, by comparing Raman spectra, Puppulin and colleagues were able to obtain an estimate of the H2O2 concentration near the biosensor.

After developing a calibration procedure for their nanosensor — relating the H2O2 concentration to a change in Raman spectrum in a quantitative way is not straightforward — the scientists were able to produce a concentration map with a resolution of about 700 nm for lung cancer cell samples. They also succeeded in extending their technique to obtain measurements of the H2O2 concentration variation across cell membranes.

The colleagues concluded that their “novel approach may be useful for the study of actual H2O2 concentrations involved in cell proliferation or death, which are fundamental to fully elucidate physiological processes and to design new therapeutic strategies”.

Image credit: ©stock.adobe.com/au/Leonid Andronov

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