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Biosensor Developed from Nanotechnology can be used for Rapid Coronavirus Testing

Biosensor Developed from Nanotechnology can be used for Rapid Coronavirus Testing
Engineers from Washington University used Nanotechnology to develop Biosensor that can be used to detect COVID-19 very quickly. (Photo: K_E_N/Shutterstock )

Engineers from the McKelvey School of Engineering at Washington University in St. Louis have received federal funding for rapid coronavirus testing using microparticles developed by the use of nanotechnology.

Srikanth Singamaneni, professor of mechanical engineering and materials science, and his group have built up a quick, profoundly delicate and exact biosensor dependent on an Ultrabright Fluorescent Nanoprobe, which can possibly be comprehensively sent.

Called a plasmonic-fluor, ultrabright fluorescent nanoprobe can also help in resource-limited situations because less complex devices are needed to read the results. The National Science Foundation has given a grant of $ 100,008 to Singamani and his team to develop a COVID-19 test using plasmonic-fluor.

Singamoney will make its plasmonic-floor-based biosensor 100 times more sensitive than the traditional SARS-CoV-2 antibody detection method. Increasing the sensitivity will allow clinicians and researchers to easily detect positive cases and reduce the possibility of false negatives.

The plasmonic-floorer works by increasing the fluorescence signal of background noise. Imagine trying to catch fireflies outside on a sunny day. You can purify one or two, but against the glare of the sun, those little bastions are hard to see. What if those fireflies had the same brightness as a high-powered flashlight?

Plasmonic-fluor effectively changes the brightness of fluorescent labels used in a variety of biosensing and bioimaging methods. For example, in addition to the COVID-19 test, it could possibly be used to diagnose that a person has had a heart attack by measuring the levels of relevant molecules in blood or urine samples.

Using plasmonic-floor, which is made of gold nanoparticles coated with conventional dyes, researchers are able to achieve up to 6,700 times brighter fluorescent nano label than conventional dyes, which could potentially lead to early diagnosis. Utilizing this nano label as an ultrabright flashlight, they have shown the discovery of amazingly modest quantities of target biomolecules on cells of biofluids and even molecules.

Beacon Gold Nanoparticles

In biomedical research and clinical laboratories, fluorescence is used as a beacon to accurately visualize and follow target biomolecules. This is an extremely useful tool, but it is not perfect.

Biosensor Developed from Nanotechnology can be used for Rapid Coronavirus Testing

'The problem with fluorescence is in many cases, it is not sufficiently acute,' Singamani said. If the fluorescent signal is not strong enough to stand out against background signals, like fireflies against the sun's glare, researchers may miss seeing something less abundant but important.

"Increasing the brightness of the nano label is extremely challenging," said the paper's lead author, Jingyi Luan. But here, it is the gold nanoparticle that sits in the center of the plasmonic-fluor that actually serves to turn the firefly into a flashlight, so to speak. 

Gold nanoparticles act as an antenna, strongly absorbed, and scattering light. This highly concentrated light funnels into the fluorophore placed around the nanoparticles. In addition to condensing light, nanoparticles accelerate the emission rate of fluorophores. Taken together, these two effects increase fluorescence emission.

Essentially, each fluorophore becomes a more efficient beacon, and 200 fluorophores sitting around the nanoparticles emit a signal that is equivalent to 6,700 fluorophores.

In addition to detecting low amounts of molecules, the sensing time can be shortened by using a plasmonic-fluor because bright beacons mean fewer captured proteins are required to determine their presence.

Researchers have also shown that plasmonic-floor allows the detection of multiple proteins simultaneously. And in flow cytometry, the luminosity effect of the plasmonic-floor allows for more precise and sensitive measurements of proteins on the cell surface, the signal of which may have been buried in background noise using conventional fluorescent tagging.

Other efforts have been made to increase fluorescent tagging in imaging, but many require the use of entirely new workflow and measurement platform. In addition to the ability of plasmonic-fluor to increase sensitivity and reduce sensing time, it does not require any changes in existing laboratory equipment or techniques.

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