TY - JOUR
T1 - Neutron Activated 153Sm Sealed in Carbon Nanocapsules for in Vivo Imaging and Tumor Radiotherapy
AU - Wang, Julie T.W.
AU - Klippstein, Rebecca
AU - Martincic, Markus
AU - Pach, Elzbieta
AU - Feldman, Robert
AU - Šefl, Martin
AU - Michel, Yves
AU - Asker, Daniel
AU - Sosabowski, Jane K.
AU - Kalbac, Martin
AU - Da Ros, Tatiana
AU - Ménard-Moyon, Cécilia
AU - Bianco, Alberto
AU - Kyriakou, Ioanna
AU - Emfietzoglou, Dimitris
AU - Saccavini, Jean Claude
AU - Ballesteros, Belén
AU - Al-Jamal, Khuloud T.
AU - Tobias, Gerard
PY - 2020/1/28
Y1 - 2020/1/28
N2 - Radiation therapy along with chemotherapy and surgery remain the main cancer treatments. Radiotherapy can be applied to patients externally (external beam radiotherapy) or internally (brachytherapy and radioisotope therapy). Previously, nanoencapsulation of radioactive crystals within carbon nanotubes, followed by end-closing, resulted in the formation of nanocapsules that allowed ultrasensitive imaging in healthy mice. Herein we report on the preparation of nanocapsules initially sealing "cold" isotopically enriched samarium (152Sm), which can then be activated on demand to their "hot" radioactive form (153Sm) by neutron irradiation. The use of "cold" isotopes avoids the need for radioactive facilities during the preparation of the nanocapsules, reduces radiation exposure to personnel, prevents the generation of nuclear waste, and evades the time constraints imposed by the decay of radionuclides. A very high specific radioactivity is achieved by neutron irradiation (up to 11.37 GBq/mg), making the "hot" nanocapsules useful not only for in vivo imaging but also therapeutically effective against lung cancer metastases after intravenous injection. The high in vivo stability of the radioactive payload, selective toxicity to cancerous tissues, and the elegant preparation method offer a paradigm for application of nanomaterials in radiotherapy.
AB - Radiation therapy along with chemotherapy and surgery remain the main cancer treatments. Radiotherapy can be applied to patients externally (external beam radiotherapy) or internally (brachytherapy and radioisotope therapy). Previously, nanoencapsulation of radioactive crystals within carbon nanotubes, followed by end-closing, resulted in the formation of nanocapsules that allowed ultrasensitive imaging in healthy mice. Herein we report on the preparation of nanocapsules initially sealing "cold" isotopically enriched samarium (152Sm), which can then be activated on demand to their "hot" radioactive form (153Sm) by neutron irradiation. The use of "cold" isotopes avoids the need for radioactive facilities during the preparation of the nanocapsules, reduces radiation exposure to personnel, prevents the generation of nuclear waste, and evades the time constraints imposed by the decay of radionuclides. A very high specific radioactivity is achieved by neutron irradiation (up to 11.37 GBq/mg), making the "hot" nanocapsules useful not only for in vivo imaging but also therapeutically effective against lung cancer metastases after intravenous injection. The high in vivo stability of the radioactive payload, selective toxicity to cancerous tissues, and the elegant preparation method offer a paradigm for application of nanomaterials in radiotherapy.
KW - cancer therapy
KW - filled carbon nanotubes
KW - nanoencapsulation
KW - nanooncology
KW - nuclear imaging
KW - radiooncology
UR - http://www.scopus.com/inward/record.url?scp=85076733884&partnerID=8YFLogxK
U2 - 10.1021/acsnano.9b04898
DO - 10.1021/acsnano.9b04898
M3 - Article
AN - SCOPUS:85076733884
SN - 1936-0851
VL - 14
SP - 129
EP - 141
JO - ACS Nano
JF - ACS Nano
IS - 1
ER -