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Scientists have created tiny metal “nanoterminators” that they hope can carry cancer drugs straight to the problem cells.
The researchers hope that the new solution can allow doctors to send treatments much more quickly to their target, potentially allowing for the treatemnet of cancer much more effectively.
The new development uses a liquid metal that is placed in a solution and then into the bloodstream, where it can attach itself to cancer cells and kill them off. Once that is done, the metal can then biodegrade.
“The advance here is that we have a drug-delivery technique that may enhance the effectiveness of the drugs being delivered, can help doctors locate tumors, can be produced in bulk, and appears to be wholly biodegradable with very low toxicity,” said Zhen Gu, one of the authors of the paper, in a statement. “And one of the advantages of this technique is that these liquid metal drug carriers – or ‘nano-terminators’ – are very easy to make.”
To make the drug, researchers put the metal into a solution that has two different molecules in it. That is then hit with ultrasound, which transforms them to make them into carriers.
Scientists can then introduce cancer drugs into the solution, take the nanodroplets and put them into the bloodstream.
Because of the way that they are created, the tiny droplets seek out cancer cells and become latched onto them. The cancer cells themselves then absorb the droplets and so sends the drug straight into the cell.
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PA
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Ye et al/Current Biology
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Reuters
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The researchers have already tested the treatment in a mouse, and found that it is far more effective than injecting it straight into the patient. There didn’t seem to be any toxic reaction from the mouse’s body, the researchers said.
“This was a proof-of-concept study, but very encouraging,” said Gu. “Like the fictional Terminator, this carrier is transformable: smashed from bulk material, fused inside cancer cells and eventually degraded and cleared. We are hoping to do additional testing in a large animal study to get closer to potential clinical trials.”
The research is published in Nature Communications.
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