The work, by researchers at the University of North Carolina at Chapel Hill in the US, has profound implications for the field of drug delivery by using red blood cells to carry drugs and then using light to release them in precise locations.
The technique, which overcomes a decades-long scientific hurdle, could drastically reduce the amount of a drug needed to treat disease and thus side effects.
"Those benefits could include avoiding surgery and the risk of infection, making anaesthesia unnecessary and allowing people to treat themselves by shining a light on a problem area, such as an arthritic knee," Lawrence said.
Lawrence and his team attached a drug molecule to vitamin B12 and loaded the compound into red blood cells, which can circulate for up to four months, providing a long-lasting reservoir of medicine that can be tapped as needed.
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They then demonstrated their ability to overcome a longtime technical hurdle: using long-wavelength light to penetrate deep enough into the body to break molecular bonds; in this case, the drug linked to vitamin B12.
To activate the drug with long-wavelength light, Lawrence and his team had to figure out how to do it in a way that required less energy.
"That's the trick, and that is where we have been successful," said Lawrence.
Lawrence's team solved the energy problem by introducing a weak energy bond between vitamin B12 and the drug and then attached a fluorescent molecule to the bond.
The fluorescent molecule acts as an antenna, capturing long wavelength light and using it to cut the bond between the drug and the vitamin carrier.
"The problem is when you start using four or five very toxic drugs you're going to have intolerable side effects," he said.
"However, by focusing powerful drugs at a specific site, it may be possible to significantly reduce or eliminate the side effects that commonly accompany cancer chemotherapy," said Lawrence.
The research was published in the journal Angewandte Chemie.
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