Cientistas da Universidade Northwestern (EUA) desenvolveram uma versão do antigo quimioterápico 5-fluorouracilo (5-FU), utilizando nanotecnologia para reestruturá-lo em Ácidos Nucleicos Esféricos (SNAs). Esta inovação permite que o medicamento seja entregue de forma altamente seletiva diretamente às células cancerígenas (como as de Leucemia Mieloide Aguda), tornando-o até 20.000 vezes mais eficaz em testes com animais e eliminando os efeitos colaterais detectáveis associados ao 5-FU tradicional, ao mesmo tempo que retarda a progressão do câncer em 59 vezes.
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00:00Scientists create a version of a cancer drug that is 20,000 times more effective and has no detectable side effects.
00:08Medical science witnesses a milestone in the fight against cancer with the announcement from Northwestern University, United States,
00:15which, through nanotechnology, managed to restructure the old chemotherapy drug 5-fluorouracil, 5-Gufu.
00:23The innovation, published in the prestigious journal ACS Nano, transforms an essential drug into a highly selective therapy, promising in terms of efficacy and safety.
00:34The success of the reformulation lies in the conversion of 5-fluorine into spherical nucleic acids, SNAs.
00:415-Fluorine, which historically has problems with low solubility and widespread toxicity, has been chemically incorporated into the DNA strands that coat tiny nanospheres.
00:52The lead researcher, Dr. Shady Amirkin, explained the mechanism, noting that unlike traditional chemotherapy drugs which attack indiscriminately,
01:01Cancer cells, especially myeloid cells like those in leukemia, overexpress receptors on their surfaces.
01:10These receptors recognize and pull the SNAs into the cell in a natural way.
01:15Once internalized, the nanostructure is broken down by enzymes, releasing the chemotherapy drug directly to the tumor site.
01:24The problem is not the medication itself, but how the body processes it.
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