Design of antibody-functionalized carbon nanotubes filled with radioactivable metals towards a targeted anticancer therapy

In the present work we have devised the synthesis of a novel promising carbon nanotube carrier for the targeted delivery of radioactivity, through a combination of endohedral and exohedral functionalization. Steam-purified single-walled carbon nanotubes (SWCNTs) have been initially filled with radio...

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Veröffentlicht in:Nanoscale 2016-07, Vol.8 (25), p.12626-12638
Hauptverfasser: Spinato, Cinzia, Perez Ruiz de Garibay, Aritz, Kierkowicz, Magdalena, Pach, Elzbieta, Martincic, Markus, Klippstein, Rebecca, Bourgognon, Maxime, Wang, Julie Tzu-Wen, Ménard-Moyon, Cécilia, Al-Jamal, Khuloud T, Ballesteros, Belén, Tobias, Gerard, Bianco, Alberto
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Sprache:eng
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Zusammenfassung:In the present work we have devised the synthesis of a novel promising carbon nanotube carrier for the targeted delivery of radioactivity, through a combination of endohedral and exohedral functionalization. Steam-purified single-walled carbon nanotubes (SWCNTs) have been initially filled with radioactive analogues ( i.e. metal halides) and sealed by high temperature treatment, affording closed-ended CNTs with the filling material confined in the inner cavity. The external functionalization of these filled CNTs was then achieved by nitrene cycloaddition and followed by the derivatization with a monoclonal antibody (Cetuximab) targeting the epidermal growth factor receptor (EGFR), overexpressed by several cancer cells. The targeting efficiency of the so-obtained conjugate was evaluated by immunostaining with a secondary antibody and by incubation of the CNTs with EGFR positive cells (U87-EGFR+), followed by flow cytometry, confocal microscopy or elemental analyses. We demonstrated that our filled and functionalized CNTs can internalize more efficiently in EGFR positive cancer cells. SWCNTs filled with radioactivable metal halides have been covalently functionalized with an antibody targeting the epidermal growth factor receptor.
ISSN:2040-3364
2040-3372
DOI:10.1039/c5nr07923c