纳米团簇
双癸酸
检出限
镧系元素
材料科学
发光
生物传感器
钐
核化学
组合化学
纳米技术
无机化学
化学
色谱法
离子
有机化学
孢子
生物
植物
光电子学
作者
Mohamed Ibrahim Halawa,Bing Shi Li,Guobao Xu
标识
DOI:10.1021/acsami.0c10069
摘要
In this study, we reported a facile, one-pot, and “green” synthesis of glutathione-protected gold nanoclusters (GSH@AuNCs) initiated by samarium (Sm3+) lanthanides for the first time. Sm3+ lanthanides more efficiently induced the formation of GSH@AuNCs with significantly enhanced luminescence than other lanthanides or heavy metal ions (Cd2+, Pb2+) did. Using this strategy, a detection for Sm3+ was made with a linearity range of (10.0–100.0 μM) and a limit of detection (LOD) of 0.5 μM. The Sm3+-based GSH@AuNCs were characterized by eco-friendliness, photostability, and low-cost synthesis with low biological toxicity and had great potential in the application for biosensing and bioimaging. They were successfully employed in the detection of dipicolinic acid (DPA), a well-reported biomarker for sensing potential infection by strongly hazardous anthrax spores. A good linear response was obtained for DPA detection ranging from 1.0 to 120.0 μM with a low LOD of 0.1 μM, which was much lower (600 times) than the infectious dosage of anthrax spores (6 × 10–5 M). The detection was due to the strong binding affinity and strong chelation capability of DPA to Sm3+ lanthanides, which caused the dissociation of the aggregates with an obvious decrease or even a turning-off effect of their luminescence.
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