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Blood cell and bacteria stuck together to deliver cancer drugs

A red blood cell stuck to a swimming E. coli bacterium can be steered using magnetism and induced to release drugs on demand – perhaps avoiding side effects
A red blood cell stuck to an E. coli
E. coli swims well, while there’s plenty of room for drugs inside a red blood cell
Alapan et al., Sci. Robot. 3, eaar4423 (2018)

A curious hybrid of a red blood cell and an E. coli bacterium could make an ideal transporter for carrying drugs inside the body.

Drug treatments often have side effects by causing changes elsewhere in the body, prompting researchers to hunt for clever ways to package drugs and target them more precisely to where they are needed. A previous effort used sperm to carry drugs towards mini tumours in a dish.

Cells of E. coli bacteria are also strong swimmers, with a spinning tail that acts like a propeller. However, these cells are small and don’t have much room for cargo. Red blood cells, meanwhile, are big and spacious, but can’t propel themselves.

Metin Sitti and colleagues at the Max Planck Institute for Intelligent Systems in Stuttgart, Germany decided to combine the two. They loaded mouse red blood cells with a cancer drug and magnetic nanoparticles, then chemically stuck them onto E. coli bacteria that had been engineered not to cause disease.

Drugs on demand

These hybrid swimmers reached speeds of around 10 micrometres per second, and were easily steered using magnetic fields. The transporter was able to squeeze through tiny channels only 3 micrometres wide, which shows that they can get to anywhere in the circulatory system, says Sitti.

So that they would release their drug cargo on demand, the microswimmers were injected with a heat-responsive dye. When they reach their target, the team used a flash of radiation to heat them up, causing them to rupture, release the drugs, and die.

If the swimmers are injected close to their target, it might take them a few hours to reach it, says Sitti. The team plans to test their swimmers in rodents next. “Depending on the results, we can apply in humans in three or four years,” says Sitti.

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