Modulation of biomimetic properties of cerium oxide nanoparticles by hypoxic tumor microenvironments: steering towards tumor specificity

The low oxygen tension characterizing the core glioblastomas (GBMs) and other solid tumors is known to cause a metabolic shift within tumors. This lowers the pH and simultaneously increases the ROS (O 2 ˙ − , HO˙, H 2 O 2 etc. ,) accumulation which eventually facilitates the tumor resistance to chem...

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Bibliographic Details
Published in:New journal of chemistry 2018, Vol.42 (8), p.6370-6380
Main Authors: Sridharan, Preethi, Vinothkumar, G., Pratheesh, Pooja, Babu, K. Suresh
Format: Article
Language:English
Subjects:
Antioxidants
Assaying
Biocompatibility
Biomimetics
Cerium oxides
In vivo methods and tests
Nanoparticles
Oxygen tension
Peroxidase
Radiation therapy
Toxicity
Tumors
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Summary:The low oxygen tension characterizing the core glioblastomas (GBMs) and other solid tumors is known to cause a metabolic shift within tumors. This lowers the pH and simultaneously increases the ROS (O 2 ˙ − , HO˙, H 2 O 2 etc. ,) accumulation which eventually facilitates the tumor resistance to chemo/radiotherapy. Herein, we report the biomimetic antioxidant properties of cerium oxide nanoparticles (CNPs) under physiological and tumor microenvironment-like conditions in vitro using a GBM cell line. CNPs were synthesized in a single step combustion method and exhibited selective cytotoxicity under tumor microenvironment-like conditions. Furthermore, the peroxidase-like activity of the CNP nanoparticles was modulated by tumor microenvironment-like conditions (pH 6.5 and 1.5% O 2 ) due to the redox transformation between the Ce 3+ ↔ Ce 4+ states of the cerium oxide nanoparticles under different conditions. When incubated with CNPs, a remarkable variation in the oxidative stress was observed from the measured MDA levels. Combined results from a peroxidase assay, MDA assay and TBARS assay revealed size and pH dependent activity which could have significant implications towards the tumor specific activity. The results are promising for the use of CNPs for tumor therapy and warrant further studies using both in vivo and in vitro models on their possible therapeutic potential.
ISSN:1144-0546
1369-9261
DOI:10.1039/C8NJ00097B