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用于 Fe 的若丹明探针:特异性识别和即时荧光生物成像的理论计算。

Rhodamine probes for Fe: theoretical calculation for specific recognition and instant fluorescent bioimaging.

机构信息

School of Pharmaceutical, Xi'an Medical University, Xi'an, Shaanxi 710021, PR China.

School of Basic Medical Sciences, Xi'an Medical University, Xi'an, Shaanxi 710021, PR China.

出版信息

Future Med Chem. 2019 Aug;11(15):1859-1869. doi: 10.4155/fmc-2019-0077. Epub 2019 Jun 26.

Abstract

To overcome the existing difficulty in distinguishing Fe(III) from Fe(II), rhodamine-containing Fe probes, giving off different fluorescence responses to ferric and ferrous ions, were synthesized. Color change in Fe recognition, accompanying spirolactam opening-closing, could be used for 'naked-eye' detection. Theoretical calculations revealed the possible Fe-probe combination mechanism. Apart from the probes' specific response toward Fe, the Fe-probe demonstrated highly quantitative relationships in fluorescence titration, instant labeling and dynamic tracking of intracellular Fe in bioimaging. Cytotoxity and bioimaging in living L929 suggested the probes' future applications as real-time detection methods for Fe in clinical diagnosis. Instant and time-lapse imagings, based on fluorescence-time stability of Fe-probe, enables the dynamic labeling and tracking of Fe in living systems.

摘要

为了克服目前在区分三价铁(Fe(III))和二价铁(Fe(II))方面的困难,合成了含有罗丹明的铁探针,它们对铁离子具有不同的荧光响应。Fe 识别伴随螺环酰胺的开环-闭环,可用于“肉眼”检测。理论计算揭示了可能的铁探针组合机制。除了探针对 Fe 的特异性响应外,该铁探针在荧光滴定、细胞内 Fe 的即时标记和动态追踪的生物成像中表现出高度定量的关系。活 L929 的细胞毒性和生物成像表明,这些探针未来可作为临床诊断中 Fe 的实时检测方法。基于 Fe 探针荧光时间稳定性的即时和时移成像,使 Fe 在活细胞系统中的动态标记和追踪成为可能。

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