Chelating decorporation agents for internal contamination by actinides: Designs, mechanisms, and advances

被引:5
|
作者
Li, Yongzhong [1 ]
Li, Bin [1 ]
Chen, Li [1 ]
Dong, Junxing [1 ]
Xia, Ziming [1 ]
Tian, Ying [1 ]
机构
[1] Beijing Inst Radiat Med, Dept Pharmaceut Sci, Beijing 100850, Peoples R China
关键词
Actinides; Internal contamination; Chelating decorporation agents; Chemical design of ligands; Chelating mechanism of ligands; Decorporating efficacy; DEPLETED URANIUM; SEQUESTERING AGENTS; TOXICITY; RATS; DETOXICATION; CALIXARENES; PLUTONIUM; CHEMISTRY; EFFICACY; NITRATE;
D O I
10.1016/j.jinorgbio.2022.112034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During the wide utilization of the actinides in medicine, energy, military, and other fields, internal contami-nations can profoundly endanger human health and public security. Chelating decorporation agents are the most effective therapies to reduce internal contamination that includes radiological and chemical toxicities. This re-view introduces the structures of chelating decorporation agents including inorganic salts, polyaminocarboxylic acids, peptides, polyphosphonates, siderophores, calixarenes, polyethylenimines, and fullerenes, and highlights ongoing advances in their designs and mechanisms. However, there are still numerous challenges that block their applications including coordination properties, pharmacokinetic properties, oral bioavailability, limited timing of administration, and toxicity. Therefore, additional efforts are needed to push novel decorporation agents with high efficiency and low toxicity for the treatment of internal contamination by actinides.
引用
收藏
页数:12
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