In vivo neutron capture therapy of cancer using ultrasmall gadolinium oxide nanoparticles with cancer-targeting ability

Gadolinium neutron capture therapy (GdNCT) is considered as a new promising cancer therapeutic technique. Nevertheless, limited GdNCT applications have been reported so far. In this study, surface-modified ultrasmall gadolinium oxide nanoparticles (UGNPs) with cancer-targeting ability ( = 1.8 nm) we...

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Veröffentlicht in:RSC advances 2020-01, Vol.10 (2), p.865-874
Hauptverfasser: Ho, Son Long, Choi, Garam, Yue, Huan, Kim, Hee-Kyung, Jung, Ki-Hye, Park, Ji Ae, Kim, Mi Hyun, Lee, Yong Jin, Kim, Jung Young, Miao, Xu, Ahmad, Mohammad Yaseen, Marasini, Shanti, Ghazanfari, Adibehalsadat, Liu, Shuwen, Chae, Kwon-Seok, Chang, Yongmin, Lee, Gang Ho
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container_end_page 874
container_issue 2
container_start_page 865
container_title RSC advances
container_volume 10
creator Ho, Son Long
Choi, Garam
Yue, Huan
Kim, Hee-Kyung
Jung, Ki-Hye
Park, Ji Ae
Kim, Mi Hyun
Lee, Yong Jin
Kim, Jung Young
Miao, Xu
Ahmad, Mohammad Yaseen
Marasini, Shanti
Ghazanfari, Adibehalsadat
Liu, Shuwen
Chae, Kwon-Seok
Chang, Yongmin
Lee, Gang Ho
description Gadolinium neutron capture therapy (GdNCT) is considered as a new promising cancer therapeutic technique. Nevertheless, limited GdNCT applications have been reported so far. In this study, surface-modified ultrasmall gadolinium oxide nanoparticles (UGNPs) with cancer-targeting ability ( = 1.8 nm) were for the first time applied to the GdNCT of cancer using nude model mice with cancer, primarily because each nanoparticle can deliver hundreds of Gd to the cancer site. For applications, the UGNPs were grafted with polyacrylic acid (PAA) for biocompatibility and colloidal stability, which was then conjugated with cancer-targeting arginylglycylaspartic acid (RGD) (shortly, RGD-PAA-UGNPs). The solution sample was intravenously administered into the tails of nude model mice with cancer. At the time of the maximum accumulation of the RGD-PAA-UGNPs at the cancer site, which was monitored using magnetic resonance imaging, the thermal neutron beam was locally irradiated onto the cancer site and the cancer growth was monitored for 25 days. The cancer growth suppression was observed due to the GdNCT effects of the RGD-PAA-UGNPs, indicating that the surface-modified UGNPs with cancer-targeting ability are potential materials applicable to the GdNCT of cancer.
doi_str_mv 10.1039/c9ra08961f
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Nevertheless, limited GdNCT applications have been reported so far. In this study, surface-modified ultrasmall gadolinium oxide nanoparticles (UGNPs) with cancer-targeting ability ( = 1.8 nm) were for the first time applied to the GdNCT of cancer using nude model mice with cancer, primarily because each nanoparticle can deliver hundreds of Gd to the cancer site. For applications, the UGNPs were grafted with polyacrylic acid (PAA) for biocompatibility and colloidal stability, which was then conjugated with cancer-targeting arginylglycylaspartic acid (RGD) (shortly, RGD-PAA-UGNPs). The solution sample was intravenously administered into the tails of nude model mice with cancer. At the time of the maximum accumulation of the RGD-PAA-UGNPs at the cancer site, which was monitored using magnetic resonance imaging, the thermal neutron beam was locally irradiated onto the cancer site and the cancer growth was monitored for 25 days. 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subjects Biocompatibility
Cancer
Chemistry
Gadolinium
Gadolinium oxide
Gadolinium oxides
Magnetic resonance imaging
Nanoparticles
Neutron beams
Nuclear capture
Polyacrylic acid
Therapy
Thermal imaging
Thermal neutrons
title In vivo neutron capture therapy of cancer using ultrasmall gadolinium oxide nanoparticles with cancer-targeting ability
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