多金属氧酸盐(POMs)新型促排剂对内污染铀促排的研究
批准号:
22106116
项目类别:
青年科学基金项目(C类)
资助金额:
30.0 万元
负责人:
王晓梅
依托单位:
学科分类:
放射化学与辐射化学
结题年份:
2024
批准年份:
2021
项目状态:
已结题
项目参与者:
王晓梅
中文摘要
锕系元素铀作为核燃料、核武器和贫铀弹等原材料,在核事故、乏燃料后处理、铀矿开采等过程中一旦发生泄露势必导致锕系元素内污染,引起内照射,导致组织损伤、癌症,甚至死亡。使用螯合剂快速螯合锕系元素并加速排出体外是减轻内污染最有效的方法,然而目前锕系元素促排剂存在毒性大、效果差及机理不明确等问题,无法满足核应急需求。多金属氧酸盐(POMs)具有结构多样性、可调变性、可修饰性以及优异的生物活性等优点广泛用于乏燃料后处理和医药等领域,然而没有锕系元素促排相关工作报道。因此,申请人提出POMs促排铀的研究思路,利用表面丰富的活性氧位点和对铀的高螯合能力等优势,提高对铀的吸附性能和选择,结合生物毒性和促排效果,利用X射线单晶衍射仪、EXAFS、IVIS成像系统等技术,直观解析POMs与铀复合物的微观结构,明确促排机理,建立构效关系,筛选出新型低毒高效的铀促排剂,为进一步优化锕系元素促排剂提供理论依据。
英文摘要
Uranium as the original material of nuclear fuel, nuclear weapon and depleted uranium bomb, would lead to the damage of tissues, organ failure, cancer and even death in the process of nuclear accidents, nuclear attraction, the reprocessing of spent nuclear fuel and uranium mining operations. To date, the most effective method to ease the internal contamination of uranium is administrated chelators, which could effectively captured uranium and accelerated the excretion of uranium in vivo. However, the existing chelators still met the defects of high toxicity, low efficacy and unclear mechanism, and no effective agents were obtained to satisfy the demand of nuclear emergency up to date. Polyoxometalates (POMs), featured with structural diversity, tunable structure, tunable functionality, and bio-compatibility, widely applied in the reprocessing of spent nuclear fuel and medical field. While POMs materials have not yet used as actinides chelators. Therefore, this project intends to synthesize lacunary polyoxometalates (POMs), taking advantage of the abundant of active oxygen sites and high chelating ability of the lacunary POMs for uranium, improving the ability of capturing and selectivity toward uranium. Subsequently, a series of in vitro and vivo assays will be performed to comprehensively evaluate the decorporation efficacy and toxicity of POMs materials, respectively, combining the X ray diffractometer, EXAFS and IVIS spectrum imaging system measurements to explore the coorderation mode of POMs and uranium complexes and clarify the mechanism of decprporation. Finally, signifying the potential application of POMs used as actinides decorporation agent for the nuclear emergency cases.
项目负责人长期从事面向我国核能可持续发展及核安全重大需求的锕系元素促排剂研究,基于锕系元素配位化学,致力于开发新型高效的锕系元素促排剂用于核事故中受污染人群核素内污染救治。本项目针对现有促排剂普遍存在毒性大、生物利用度低、促排效果有限等问题,项目负责人提出了POMs材料用于体内铀污染促排的研究,利用表面丰富的活性氧位点和对铀的高螯合能力等优势,提高对铀的选择性和促排效率。项目负责人首先采用匹配铀配位模式的策略合成制备了缺位多金属氧酸盐材料PW9和Se6W45,赋予其铀促排和辐射防护双重功能,利用X-射线单晶衍射仪明确了POMs与铀的配位模式,相比于两个PW9与两个铀酰离子形成的三明治夹心结构,Se6W45精准匹配了铀酰离子赤道面配位需求,实现了Se6W45超低剂量比下铀的高效促排。随后,采用增加活性氧位点的策略制备了环状缺位多金属氧酸盐P8W48,该材料在生理条件下可快速聚集并被动靶向于肺组织,在肺促排方面具有显著优势。同时,在本项目的支持下,探索了新型小分子促排剂和纳米框架材料促排体系,均在肾脏中铀促排和肺组织中铀促排取得了具有代表性的成果。以上成果为核应急救治提供了技术支持,为锕系元素促排剂的设计优化提供了理论指导。
响应性聚集的新型纳米MOFs促排剂用于肺呼吸暴露铀内污染促排的研究
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批准号:22376155
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项目类别:面上项目
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资助金额:50万元
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批准年份:2023
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负责人:王晓梅
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依托单位:
多金属氧酸盐(POMs)新型促排剂对内污染铀促排的研究
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批准号:--
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项目类别:--
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资助金额:30万元
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批准年份:2021
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负责人:王晓梅
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依托单位:
国内基金
海外基金