Nanotubes: a new vehicle for targeted drug delivery
Grant Information
Institute - Imperial College London
Researcher - Dr Robert Kypta
Grant Award - £157,116
Duration of Funding - 2022-2024
Status - Complete
Reference - RIA19-ST2-009
We envision a new type of therapy for men with prostate cancer, one that delivers specific and effective drugs that are only toxic to cancer cells, thus avoiding side effects.
Why did we fund this project?
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While current treatments for prostate cancer can be very effective at killing prostate cancer cells, they can also damage healthy cells, leading to challenging side effects for men.
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Dr Robert Kypta, Dr Fang Xie and Professor Alexandra Porter from Imperial College London joined forces to develop a way to deliver drugs directly to prostate cancer cells, helping to protect healthy cells.
What did the researchers do?
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The team first created tiny tubes, called nanotubes, and loaded them with a drug that is known to kill prostate cancer cells.
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They then developed a molecule that can recognise prostate cancer cells and attached it to the surface of the nanotubes, allowing the drug to be delivered directly to prostate cancer cells.
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Finally, the researchers tested whether the nanotubes could reach prostate cancer cells, release the drug and slow the growth of prostate cancer cells.
What did the researchers achieve?
- The team successfully created nanotubes that are safe, can break down in the body, and can carry large amounts of a drug.
- The specially developed molecule on the surface of the nanotubes helped them target prostate cancer cells and slow their growth.
How will this benefit men?
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If clinical trials are successful, nanotubes could be used to deliver many different types of drugs directly to prostate cancer cells.
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This targeted approach could help men avoid unnecessary side effects, ultimately improving quality of life for men living with prostate cancer.
Help us fund more research like this
Your donation helps us fund lifesaving research into better ways to diagnose prostate cancer.