铀
生物相容性
体内
壳聚糖
化学
核化学
药理学
螯合作用
放射化学
材料科学
生物化学
有机化学
生物技术
医学
冶金
生物
作者
Zhiheng Li,Siyi Wang,Yipu Dong,Xiaoyao Miao,Bingkun Xiao,Jianyun Yang,Jianfeng Zhao,Rongqing Huang
标识
DOI:10.1016/j.ecoenv.2022.113636
摘要
Amidoxime functionalized chitosan (AC) was recommended as a chelator for uranium sequestration in vivo in this study, and the structure-activity relationship was also explored. Compared with ZnNa 3 -DTPA, which was a commercial uranium mobilization drug, AC exhibited excellent biocompatibility and uranium removal efficiency, whether by injection or orally, which could reduce the amounts of uranium deposited in kidneys and femurs by up to 43.6% and 32.3%. In particular, ACs still possessed the ability to mobilize uranium in vivo even if administration was delayed for 72 h. • Amidoxime functionalized chitosan (AC) exhibit excellent biocompatibility. • AC successfully reduce the concentration of uranium in vivo , whether by injection or orally. • The particle size is a crucial factor that affects the removal efficiency of uranium mobilization drug.
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