摘要
Described here is that Au−C≡C bonds showed the highest stability under biological conditions, with abundant thiols, and the best electrochemical performance compared to Au−S and Au−Se bonds. The new finding was also confirmed by theorical calculations. Based on this finding, a specific molecule for recognition of Fe2+ was designed and synthesized, and used to create a selective and accurate electrochemical sensor for the quantification of Fe2+. The present ratiometric strategy demonstrates high spatial resolution for real-time tracking of Fe2+ in a dynamic range of 0.2–120 μM. Finally, a microelectrode array with good biocompatibility was applied in imaging and biosensing of Fe2+ in the different regions of live mouse brains. Using this tool, it was discovered that the uptake of extracellular Fe2+ into the cortex and striatum was largely mediated by cyclic adenosine monophosphate (cAMP) through the CREB-related pathway in the brain of a mouse with Alzheimer's disease.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 20499-20507 |
| 页数 | 9 |
| 期刊 | Angewandte Chemie - International Edition |
| 卷 | 59 |
| 期 | 46 |
| DOI | |
| 出版状态 | 已出版 - 9 11月 2020 |
指纹
探究 'A Robust Au−C≡C Functionalized Surface: Toward Real-Time Mapping and Accurate Quantification of Fe2+ in the Brains of Live AD Mouse Models' 的科研主题。它们共同构成独一无二的指纹。引用此
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