在安全的可持续溶剂中吸收含有核苷酸的食物/水容器中的重金属

Nidhi Sharma
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引用次数: 0

摘要

重金属沉积对气候变化和生态系统生存构成严重威胁。重金属的生物积累对人体各器官和组织是慢性的。重金属暴露主要通过食物和水发生。在食物和水容器中使用的重金属导致它们浸出到液体和食物中。重金属的持续工业释放引发了作为金属螯合剂的杂环的大量合成。本研究以三唑为原料,与胞苷和鸟嘌呤在室温下制备了三唑-核苷和三唑-核苷酸杂种T1和T2。通过核磁共振、紫外和高效液相色谱滴定研究了探针与Cu2+、Ni2+、Zn2+、Mn2+和Pb2+离子的金属结合亲和力。最低检出限为20 ng/ml。金属结合后T1在母光谱218.5 ~ 254.5 nm和T2在290 ~ 312.5 nm之间形成红移峰,表明金属结合具有选择性。在物理环境和生物基质的重金属解毒过程中,检出限(Lod)起着至关重要的定量作用。金属捕获量的递增顺序为T1......Ni2+ >;T2……Ni2 +比;T1……Pb2 +比;T2……Pb2+见负载值。该订单进一步扩大了探针在生物基安全溶剂(即水乙腈)中用于食品和水安全的金属传感中的选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Absorption of heavy metals present in food/water containers with nucleotides in safe sustainable solvents
Heavy metal deposition poses a serious risk to climate change and ecosystem survival. Bio accumulation of heavy metals is chronic to various body organs and tissues. Heavy metal exposure mainly occurs through food and water. Heavy metals used in food and water containers lead to their leaching into the liquids and foods. The continuous industrial release of heavy metals triggers massive synthesis of hetero cycles as metal chelators. In this study, triazole-nucleoside and triazole-nucleotide hybrids, viz., T1 and T2, were prepared from triazole with cytidine and guanine at room temperature. The probes were studied for metal binding affinity with Cu2+, Ni2+, Zn2+, Mn2+, and Pb2+ ions with NMR, UV, and HPLC titrations. The lowest detection limit is 20 ng/ml. The formation of red-shifted peaks between 218.5 to 254.5 nm in the parent spectrum of T1 and between 290 and 312.5 nm of T2 after metal binding showed the selectivity in binding. In heavy metal detoxification of physical environment and bio matrix, the limit of detection (Lod) plays a crucial quantitative role. The increasing order of metal capture is T1……Ni2+ > T2…….Ni2+ > T1……Pb2+ > T2……..Pb2+ as seen in Lod values. This order further amplifies the selective nature of probes in metal sensing for food and water safety in bio based safe solvent viz., aqueous acetonitrile.
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CiteScore
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