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Table 3 Recently studied radionuclide delivery systems based on inorganic NPs

From: Current outlook on radionuclide delivery systems: from design consideration to translation into clinics

Radionuclide

Delivery system

Labeling

Application

Comments

Refs.

225Ac

Gold coated lanthanide phosphate NPs

‘Hot’ + ‘cold’ precursor

Radiotherapy

McLaughlin et al. developed multilayered NPs that can deliver multiple a radiations and contain the decay daughters of 225Ac while targeting biologically relevant receptors in a female BALB/c mouse model

[200]

198Au

Au NPs

‘Hot’ + ‘cold’ precursor

Radiotherapy

Katti et al. developed a novel approach to treat prostate cancer with 198Au NPs, which were modified with glucoside molecules mangiferin. In vivo experiments on severe combined immunodeficient (SCID) mice revealed over 85% reduction of bearing prostate tumor volume as compared to the control groups

[201]

166Ho

Garnet magnetic NPs

Neutron activation

Radiotherapy

Munaweera et al. developed magnetic NPs, which were modified with 165Ho/cytostatic drug and navigated into tumor area using external magnet. In vitro and in vivo results suggested that the external magnetic field navigation was achieved, since higher amounts of 165Ho were observed in tumor than in liver, which led to the inhibition of tumor growth

[206]

89Zr

Ultrasmall silica NPs

Chelation (DFO)

PET and optic imaging

Chen et al. described synthesis of a PEGylated ultrasmall silica particles labeled with Cy5 dye. Reported NPs were modified with chelators and anti-HER2 scFv fragments. This allowed to achieve more efficient tumor-targeting with bulk renal clearance, which surpasses already existing characteristics of scFv molecules and scFv-conjugated NPs larger than 10 nm. The experiments in vivo revealed a favorable pharmacokinetics and clearance with decreased hepatic and reticuloendothelial system uptake

[212]

99mTc

Mesoporous silica NPs

Reduction of Tc(VII) in TcO4− using SnCl2

SPECT

Pascual et al. improved targeting properties of developed Si-based systems by functionalization of NPs with Mucin 1 aptamer that is specific to breast cancer. Pronounced targeted delivery of 99mTc into tumor of tumor-bearing Balb/c mice was shown and monitored with SPECT and bioluminescence options

[214]

89Zr

Mesoporous silica NPs

Chelation with the deprotonated silanol groups

Photodynamic therapy

Kamkaew et al. reported mesoporous silica NPs loaded with 89Zr and photosensitizer Chlorin e6, which can be activated by Cherenkov radiation from 89Zr. Therefore, the developed radionuclide delivery systems overcame the limitations of conventional photodynamic therapy, which requires light source to activate photosensitizer

[216]

225Ac

CNT

Chelation (DOTA)

Radiotherapy

Ruggiero et al. developed CNT-based carriers to deliver 225Ac into the tumor angiogenic vessels, which express the monomeric vascular endothelial-cadherin. The developed carrier system was able to achieve 100-fold amplified cargo delivery (relative to the gold standard for targeted therapy—IgG)

[223]

131I

Reduced graphene oxide

Standard chloramine-T oxidation method

Photothermal and radiotherapy

Chen et al. developed radio-labeled graphene-derivative, which offers the ability of in vivo tumor imaging, and is able to deliver both photothermal and radiotherapy at the same time in order to achieve synergistic therapeutic effect using a single nanoscale theranostic agent

[226]