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Implantable ‘living materials’ that deliver drugs on demand could help fight infections

In a “breakthrough,” researchers demonstrate how engineered bacteria held in a jellylike container could help fight infection in mice

Illustration of Escherichia coli bacteria

In “living materials,” bacteria such as Escherichia coli could be engineered to sense and fight pathogens.

THOM LEACH/SCIENCE PHOTO LIBRARY/Getty Images

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To treat an infection, doctors have to find and diagnose it first. But a new approach involving what researchers are calling “living materials” could fundamentally change that. Designed to sit inside your body and activate when needed to help fight infections at the source, the strategy could dispense with the need for pills, shots and even diagnostics.

In a new study published in Science on Thursday, researchers describe successfully implanting a mouse with a “living material” made with genetically engineered bacteria to treat an infection. The technology, if validated in humans, could be used to help prevent infection in surgeries or as a long-term therapeutic that automatically responds to pathogens.

“Living” medicine isn’t totally new. Scientists already knew that bacteria can be programmed to sense pathogens and self-destruct when they do so, releasing drugs to kill the invader.


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But researchers have been wary about such approaches. “One of the big concerns that everyone has is that we’re injecting live bacteria into our body,” says Tetsuhiro Harimoto, the study’s lead author and a postdoctoral fellow at Harvard University. “We don’t want them to disseminate and cause infections.”

To solve the problem, Harimoto and his colleagues built a “hydrogel,” or jellylike, container. It’s permeable like a mesh yet stiff enough to contain a live and growing population of bacteria without bursting open and strong enough to withstand some wear and tear. The material is similar to the tapioca pearls you might find in boba tea but stiffer, Harimoto says.

To ensure the bacteria wouldn’t escape their hydrogel cage, the researchers ran the hydrogel through a series of stress tests, such as a “fatigue” experiment—in which they stretched the capsule 10,000 times to see if it would break—and let it sit for six months in a “nutrient broth,” Harimoto says.

“Every week or two, we’d basically go in and sample the broth and see if any bacteria [had] come out,” Harimoto says. “At some point, we’re like, ‘Okay, I think this is going to work.’”

a round blob that darkens over time

Bacterial growth in a hydrogel. The scale bar represents 50 microns.

The final test involved putting the hydrogel into a mouse. Much like a doctor might put a prosthetic pin in a broken bone to help it heal, the team performed a similar surgery in mice. Some of the rodents received a prosthetic pin treated with a “living” hydrogel that had bacteria designed to detect a pathogen, Pseudomonas aeruginosa, while others didn’t get the treated pin.

To simulate an infection, the researchers also introduced P. aeruginosa to the surgery site. In mice implanted with the “living” hydrogel, the pathogen had a harder time replicating. “We saw a big difference between the one that’s treated with engineered living materials and the one that’s treated with no therapeutics,” Harimoto says.

The results suggest that hydrogels could be used to contain engineered, infection-fighting bacteria for months at a time—a first, says Quanyin Hu, an associate professor in the School of Pharmacy at the University of Wisconsin–Madison, who co-authored a related commentary in Science but was not involved in the study. “The major breakthrough of this study is they can contain these bacteria in the implantation site without the bacteria leaking,” he says.

In theory, Hu says, they technology could also be used to help prevent tumors from coming back, treat inflammation or administer other drugs.

That work is already on the way: in August Harimoto plans to start a lab at Cornell University to test other applications for these programmable “living materials,” including for conditions such as cancer. “Some of the things that we’re excited about [are] to really apply this to a variety of different diseases,” he says.

Jackie Flynn Mogensen is a breaking news reporter at Scientific American. Before joining SciAm, she was a science reporter at Mother Jones, where she received a National Academies Eric and Wendy Schmidt Award for Excellence in Science Communications in 2024. Mogensen holds a master’s degree in environmental communication and a bachelor’s degree in earth sciences from Stanford University. She is based in New York City.

More by Jackie Flynn Mogensen

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