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• W2012352088 abstract "Single-walled carbon nanotubes (SWNTs) can deliver imaging agents or drugs to tumours and offer significant advantages over approaches based on antibodies or other nanomaterials. In particular, the nanotubes can carry a substantial amount of cargo (100 times more than a monoclonal antibody), but can still be rapidly eliminated from the circulation by renal filtration, like a small molecule, due to their high aspect ratio. Here we show that SWNTs can target tumours in a two-step approach in which nanotubes modified with morpholino oligonucleotide sequences bind to cancer cells that have been pretargeted with antibodies modified with oligonucleotide strands complementary to those on the nanotubes. The nanotubes can carry fluorophores or radioisotopes, and are shown to selectively bind to cancer cells in vitro and in tumour-bearing xenografted mice. The binding process is also found to lead to antigen capping and internalization of the antibody–nanotube complexes. The nanotube conjugates were labelled with both alpha-particle and gamma-ray emitting isotopes, at high specific activities. Conjugates labelled with alpha-particle-generating 225Ac were found to clear rapidly, thus mitigating radioisotope toxicity, and were shown to be therapeutically effective in vivo. Single-walled carbon nanotubes can target tumours in a two-step approach in which nanotubes modified with morpholino oligonucleotide sequences bind to cancer cells that have been pre-targeted with antibodies modified with oligonucleotide strands complementary to those on the nanotubes." @default.
• W2012352088 created "2016-06-24" @default.
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• W2012352088 date "2013-09-29" @default.
• W2012352088 modified "2023-10-16" @default.
• W2012352088 title "Self-assembly of carbon nanotubes and antibodies on tumours for targeted amplified delivery" @default.
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• W2012352088 doi "https://doi.org/10.1038/nnano.2013.190" @default.
• W2012352088 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3798027" @default.
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