Source abstract
Abstract
In response to diffused ionizing radiation damage throughout the body caused by nuclear leaks and inaccurate radiotherapy, radioprotectants with considerable free radical scavenging capacities, along with negligible adverse effects, are highly regarded. Herein, unlike being performed as toxic chemotherapeutic drug candidates, molybdenum-based polyoxometalate nanoclusters (Mo-POM NCs) were developed as a non-toxic potent radioprotectant with impressive free radical scavenging capacities for ionizing radiation protection. In comparison to the clinically used radioprotectant drug amifostine (AM), the as-prepared Mo-POM NCs exhibited effective shielding capacity by virtue of their antioxidant properties resulting from a valence shift of molybdenum ions, alleviating not only ionizing radiation-induced DNA damage but also disruption of the radiation-sensitive hematopoietic system. More encouragingly, without trouble with long-term retention in the body, ultra-small sized Mo-POM NCs prepared by the mimetic Folin-Ciocalteu assay can be removed from the body through the renal-urinary pathway and the hepato-enteral excretory system after completing the mission of radiation protection. This work broadened the biological applications of metal-based POM chemotherapeutic drugs to act as a neozoic radioprotectant.
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Affiliations
The First Affiliated Hospital of USTC, School of Life Sciences and Medicine, University of Science and Technology of China, Hefei230031, P. R. China
Department of Radiation Oncology, Anhui Provincial Cancer Hospital, Hefei230031, P. R. China
School of Food and Biological Engineering, Hefei University of Technology, Hefei230009, P. R. China
International Immunology Center, Anhui Agricultural University, Hefei230036, P. R. China
Funding
the University Synergy Innovation Program of Anhui Province · Chinese Medicine Education Association