Speeding Up Diagnosis

A new nanoparticle-based tool could provide a faster, easier way to identify infections.

A startup based in Cambridge, MA, is commercializing a new kind of rapid diagnostic technology that relies on magnetic nanoparticles and a technique similar to magnetic resonance imaging (MRI). The nanoparticles can be designed to signal the presence of specific viruses and bacteria, particular strands of DNA and proteins including those found on cancer cells, and other molecules such as glucose. The technique can use blood, spit, or any other samples with no preparation. The researchers hope the tool will help doctors identify treatments faster and allow for better monitoring of cancer treatments.

Detecting disease: A new diagnostic system uses magnetic nanoparticles to detect biomarkers, bacteria, and viruses. The wells of liquid in this MRI image contain nanoparticles targeted to particular strands of RNA. The greenish well shows a signal resulting from the detection of a brain-cancer cell. The additional wells contain sensing nanoparticles and other cancer cells. Credit: Ralph Weissleder, Harvard Center for Molecular Imaging Research

The company, T2 Biosystems, expects to begin marketing diagnostics for infectious diseases in two years, and it's developing implantable sensors and handheld readers for monitoring diseases such as diabetes and cancer. Prominent researchers from MIT, Harvard, and Massachusetts General Hospital founded the company. Tyler Jacks, director of the MIT Center for Cancer Research and a cofounder of T2, says that the company is developing "more rapid, accurate, portable, and cheaper diagnostics."

The new diagnostic is based on iron-oxide nanoparticles that generate a strong magnetic signal when exposed to a magnetic field. Each nanoparticle resembles a spiky ball and is coated with molecules like antibodies or single strands of DNA that bind to a specific target. The researchers can design nanoparticles to target just about any molecule. In the absence of the target, the nanoparticles float freely in solution. When the nanoparticles are put in a solution containing the target molecule, they aggregate, each nanoparticle binding to multiple target molecules and creating tangled clumps. The nanoparticles make a different kind of magnetic signal when clumped. This signal can be read in an MRI machine or in a relaxometer, a desktop-sized device.

The nanoparticles were developed by company cofounders Ralph Weissleder, director of the Center for Molecular Imaging Research at Harvard, and Lee Josephson, associate professor of radiology at Harvard Medical School. Josephson says that the key advantage to T2 Biosystems' diagnostic is that it doesn't rely on optical signals. Traditional biochemical diagnostic techniques all require extensive sample processing because light doesn't travel well through the body or through opaque liquids like blood, which must therefore be purified. The signal created by the magnetic nanoparticles does.

Story continues below

No preparation is necessary for T2 Biosystems' tests. A sample is simply combined with the nanoparticles and put in the relaxometer to take a reading. (Relaxometers are commercially available and could be incorporated into hospital laboratories.)

Josephson expects the nanoparticle diagnostic to have a "very large advantage over the state of the art" in the area of infectious disease. He and Weissleder have used the nanoparticles to identify, among other pathogens, common viruses including herpes simplex and adenoviruses, as well as the bacteria that cause tuberculosis. Identifying the cause of a patient's infection using traditional means, such as culturing bacteria, can require a great deal of time, says Josephson. Genomic techniques for identifying viruses and bacterial strains, such as PCR, also require sample preparation. The sooner the pathogen is identified, the sooner the patient can be given the right antibiotic or isolated and prevented from infecting other people. This is especially important in the case of a viral outbreak like SARS or influenza, or when a patient harboring drug-resistant bacteria enters a hospital.