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Article: Neutron-irradiated antibody-functionalised carbon nanocapsules for targeted cancer radiotherapy

TitleNeutron-irradiated antibody-functionalised carbon nanocapsules for targeted cancer radiotherapy
Authors
Issue Date2020
Citation
Carbon, 2020, v. 162, p. 410-422 How to Cite?
AbstractRadiotherapy is a cancer treatment utilising high doses of ionizing radiation to destroy cancer cells. Our team has pioneered neutron activation of 152Sm, filled and sealed into single-walled (SWCNTs) and multi-walled carbon nanotubes (MWCNTs), to create stable and high-dose radioactive carbon nanocapsules for cancer radiotherapy. In this work, MWCNTs filled with enriched 152SmCl3 (Sm@MWCNTs) were sealed and irradiated, followed by surface functionalisation with an epidermal growth factor receptor (EGFR)-targeting antibody. Characterisation of functionalised Sm@MWCNTs was carried out using thermogravimetric analysis, gel electrophoresis and transmission electron microscopy. The organ biodistribution of the radioactive functionalised 153Sm@MWCNTs and therapeutic efficacy were studied in an experimental melanoma lung metastatic tumour model in mice after intravenous injection. Quantitative biodistribution analyses showed high accumulation of 153Sm@MWCNT-Ab in lung. Significant tumour growth reduction was induced by both treatments of 153Sm@MWCNTs functionalised with or without the antibody after a single intravenous injection. Although EGFR targeting showed no improvement in therapeutic efficacy, reduced spleen toxicity and normal haematological profiles were obtained for both functionalised derivatives. The current study demonstrated the possibility of performing chemical functionalisation and antibody conjugation on radioactive nanocapsules post-irradiation for the preparation of targeted radiopharmaceuticals.
Persistent Identifierhttp://hdl.handle.net/10722/349406
ISSN
2023 Impact Factor: 10.5
2023 SCImago Journal Rankings: 2.171

 

DC FieldValueLanguage
dc.contributor.authorWang, Julie Tzu Wen-
dc.contributor.authorSpinato, Cinzia-
dc.contributor.authorKlippstein, Rebecca-
dc.contributor.authorCosta, Pedro Miguel-
dc.contributor.authorMartincic, Markus-
dc.contributor.authorPach, Elzbieta-
dc.contributor.authorRuiz de Garibay, Aritz Perez-
dc.contributor.authorMénard-Moyon, Cécilia-
dc.contributor.authorFeldman, Robert-
dc.contributor.authorMichel, Yves-
dc.contributor.authorŠefl, Martin-
dc.contributor.authorKyriakou, Ioanna-
dc.contributor.authorEmfietzoglou, Dimitris-
dc.contributor.authorSaccavini, Jean Claude-
dc.contributor.authorBallesteros, Belén-
dc.contributor.authorTobias, Gerard-
dc.contributor.authorBianco, Alberto-
dc.contributor.authorAl-Jamal, Khuloud T.-
dc.date.accessioned2024-10-17T06:58:19Z-
dc.date.available2024-10-17T06:58:19Z-
dc.date.issued2020-
dc.identifier.citationCarbon, 2020, v. 162, p. 410-422-
dc.identifier.issn0008-6223-
dc.identifier.urihttp://hdl.handle.net/10722/349406-
dc.description.abstractRadiotherapy is a cancer treatment utilising high doses of ionizing radiation to destroy cancer cells. Our team has pioneered neutron activation of 152Sm, filled and sealed into single-walled (SWCNTs) and multi-walled carbon nanotubes (MWCNTs), to create stable and high-dose radioactive carbon nanocapsules for cancer radiotherapy. In this work, MWCNTs filled with enriched 152SmCl3 (Sm@MWCNTs) were sealed and irradiated, followed by surface functionalisation with an epidermal growth factor receptor (EGFR)-targeting antibody. Characterisation of functionalised Sm@MWCNTs was carried out using thermogravimetric analysis, gel electrophoresis and transmission electron microscopy. The organ biodistribution of the radioactive functionalised 153Sm@MWCNTs and therapeutic efficacy were studied in an experimental melanoma lung metastatic tumour model in mice after intravenous injection. Quantitative biodistribution analyses showed high accumulation of 153Sm@MWCNT-Ab in lung. Significant tumour growth reduction was induced by both treatments of 153Sm@MWCNTs functionalised with or without the antibody after a single intravenous injection. Although EGFR targeting showed no improvement in therapeutic efficacy, reduced spleen toxicity and normal haematological profiles were obtained for both functionalised derivatives. The current study demonstrated the possibility of performing chemical functionalisation and antibody conjugation on radioactive nanocapsules post-irradiation for the preparation of targeted radiopharmaceuticals.-
dc.languageeng-
dc.relation.ispartofCarbon-
dc.titleNeutron-irradiated antibody-functionalised carbon nanocapsules for targeted cancer radiotherapy-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.carbon.2020.02.060-
dc.identifier.scopuseid_2-s2.0-85080152127-
dc.identifier.volume162-
dc.identifier.spage410-
dc.identifier.epage422-

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