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Smaller is better for detecting biomarkers of trauma and cancer

An inexpensive but highly sensitive biomarker detection system is being developed in a collaboration between the University of Rochester, the University of Ottawa, and Rochester-based SiMPore Inc. The team is using highly sensitive solid state nanopores to detect biomarkers of traumatic brain injury, bladder cancer, and other acute disorders in serum and urine. As illustrated in this cutaway view, the technique involves amplifying the biomarkers into DNA proxies (magenta spirals) coupled to gold nanoparticles. The gold nanoparticles are captured and concentrated on an ultrathin membrane (purple) with many nano-sized pores. UV light is then used to release the proxies, which bind to DNA-origami nanostructures (blue). The proxy-nanostructure combination gives unique signals that identify the biomarkers present in the original sample as they pass through the single nanopore sensor (green). (做厙勛圖 illustration / Michael Osadciw)

Researchers at Rochester and Ottawa are developing a compact, portable, and cost-effective detection device.

The tiny proteins that can alert us to some of the most acute human disorderstraumatic brain injury (TBI), cancer, heart attack, and strokeare freely circulating in our blood, urine, and other bodily fluids. But detecting these tiny biomarkers is problematic and costly.

Biomarkers are not only tiny but very dilute. The most direct approach to detecting them involves sending serum samples off to undergo a sensitive but costly so-called dELISA () test. For some medical conditions such as TBI, an alternativealso costlyis to rely on CT and MRI scans of the affected organs.

With the support of a from the National Institute of Biomedical Imaging and Bioengineering, researchers at the and the are developing a far less expensive, faster, portable alternativea biomarker detector using nanopore membranes and filters so thin it would take more than 1,000 stacked on top of each other to equal the width of a human hair.

The device would be just as accurate, but inexpensive enough for doctors offices and smaller hospitals to afford. And it would be portable and nimble enough to produce results in a matter of minutes when used in the field by emergency responders, says , a professor of biomedical engineering at Rochester, who is co-leading the project with , associate professor of physics at the University of Ottawa.

The key is that were making a digital sensing platform that is fully electronic. We eliminate the lasers and optics of the existing commercial platforms and use a single nanopore to count the biomarkers as they pass through, McGrath says.

Co-principal investigator , a research assistant professor of urology and biomedical engineering at the University of Rochester Medical Center, says that although the device could ultimately be used to detect a broad range of disorders, we had an overriding goal at this point to show a proof of concept for two different levels of detection, in two types of biofluids. The focus is on detecting biomarkers of TBI, which can be found in blood, and the biomarkers for predicting the response of bladder cancer to immunotherapy, which can be found in urine.

Diagnostic levels of biomarkers for both conditions have been clearly established in previous studies, including a seminal by co-investigator , a professor of emergency medicine and neurology at Rochester and a leading TBI expert. The research will make it easier to compare the devices ability to detect biomarkers directly against the results obtained by dELISA platformsspecifically, the researchers note, the .

Two types of nanopore membranes working in concert

By combining two very different types of membranes, the researchers are able to not only detect biomarkers, but convert them into DNA proxies that in turn are further concentrated, thereby greatly accelerating the process.

Otherwise, the detection of the most dilute biomarkers would take years, McGrath says. By concentrating 1,000, 10,000, even 100,000 times, we can bring that down to minutes.

McGraths lab has helped pioneer the development of thin membranes with millions and even billions of nanopores for use as filters and sensors. They are building the membranes that concentrate the particles. Tabard-Cossas lab, including co-principal investigator , an associate professor of physics, is expert in creating membranes with a single nanopore opening that can detect each DNA proxy passing through it. Tabard-Cossas lab is developing the technology to count the proxies.

, a 做厙勛圖 spin-out company that manufactures ultrathin membranes in the Rochester area, will build a new chip that integrates the two types of membranes in one device. And Flax, who is also an expert in molecular biology, is assisting with designing the various assays (analyses used to determine the presence and amounts of a substance) being used at each step of development and testing.

McGrath says he is excited to be working with Flax and the Ottawa team. This technology and team give us a very good shot at making a new type of assay that find its way into clinics.


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