Brachytherapy at the nanoscale with protein functionalized and intrinsically radiolabeled [169Yb]Yb2O3 nanoseeds.

Purpose: Classical brachytherapy of solid malignant tumors is an invasive procedure which often results in an uneven dose distribution, while requiring surgical removal of sealed radioactive seed sources after a certain period of time. To circumvent these issues, we report the synthesis of intrinsic...

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Publicado en:European Journal of Nuclear Medicine & Molecular Imaging Vol. 51; no. 6; pp. 1558 - 1574
Autores principales: Ghosh, Sanchita, Patra, Sourav, Younis, Muhsin H., Chakraborty, Avik, Guleria, Apurav, Gupta, Santosh K., Singh, Khajan, Rakhshit, Sutapa, Chakraborty, Sudipta, Cai, Weibo, Chakravarty, Rubel
Formato: Journal Article
Publicado: Springer Nature May2024
Acceso en línea:Ver este registro en EBSCOhost
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      dt: May2024
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      pub: Springer Nature
      place: New York, New York
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        174999548
        10.1007/s00259-024-06612-1
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        atl: Brachytherapy at the nanoscale with protein functionalized and intrinsically radiolabeled [169Yb]Yb2O3 nanoseeds.
      aug:
        au:
          Ghosh, Sanchita
          Patra, Sourav
          Younis, Muhsin H.
          Chakraborty, Avik
          Guleria, Apurav
          Gupta, Santosh K.
          Singh, Khajan
          Rakhshit, Sutapa
          Chakraborty, Sudipta
          Cai, Weibo
          Chakravarty, Rubel
        affil: https://ror.org/05w6wfp17 Radiopharmaceuticals Division, Bhabha Atomic Research Centre, 400085, Trombay, Mumbai, India
      sug:
      ab: Purpose: Classical brachytherapy of solid malignant tumors is an invasive procedure which often results in an uneven dose distribution, while requiring surgical removal of sealed radioactive seed sources after a certain period of time. To circumvent these issues, we report the synthesis of intrinsically radiolabeled and gum Arabic glycoprotein functionalized [169Yb]Yb2O3 nanoseeds as a novel nanoscale brachytherapy agent, which could directly be administered via intratumoral injection for tumor therapy. Methods: 169Yb (T½ = 32 days) was produced by neutron irradiation of enriched (15.2% in 168Yb) Yb2O3 target in a nuclear reactor, radiochemically converted to [169Yb]YbCl3 and used for nanoparticle (NP) synthesis. Intrinsically radiolabeled NP were synthesized by controlled hydrolysis of Yb3+ ions in gum Arabic glycoprotein medium. In vivo SPECT/CT imaging, autoradiography, and biodistribution studies were performed after intratumoral injection of radiolabeled NP in B16F10 tumor bearing C57BL/6 mice. Systematic tumor regression studies and histopathological analyses were performed to demonstrate therapeutic efficacy in the same mice model. Results: The nanoformulation was a clear solution having high colloidal and radiochemical stability. Uniform distribution and retention of the radiolabeled nanoformulation in the tumor mass were observed via SPECT/CT imaging and autoradiography studies. In a tumor regression study, tumor growth was significantly arrested with different doses of radiolabeled NP compared to the control and the best treatment effect was observed with ~ 27.8 MBq dose. In histopathological analysis, loss of mitotic cells was apparent in tumor tissue of treated groups, whereas no significant damage in kidney, lungs, and liver tissue morphology was observed. Conclusions: These results hold promise for nanoscale brachytherapy to become a clinically practical treatment modality for unresectable solid cancers.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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