Rhodamine probes for Fe3+: theoretical calculation for specific recognition and instant fluorescent bioimaging

被引:6
作者
Cheng, Zhao [1 ]
Zheng, Lei [1 ]
Liang, Fei [1 ]
He, Hao [1 ]
Xu, Hao [2 ]
Pang, Long [2 ]
机构
[1] Xian Med Univ, Sch Pharmaceut, Xian 710021, Shaanxi, Peoples R China
[2] Xian Med Univ, Sch Basic Med Sci, Xian 710021, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
intracellular labeling; naked-eye detection; theoretical calculation; GRAPHENE QUANTUM DOTS; SENSITIVE DETECTION; SELECTIVE DETECTION; CHEMOSENSOR; CELLS; IONS; CU2+; HG2+; NITROGEN; SENSORS;
D O I
10.4155/fmc-2019-0077
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aim: To overcome the existing difficulty in distinguishing Fe(III) from Fe(II), rhodamine-containing Fe3+ probes, giving off different fluorescence responses to ferric and ferrous ions, were synthesized. Materials & methods: Color change in Fe3+ recognition, accompanying spirolactam opening-closing, could be used for 'naked-eye' detection. Theoretical calculations revealed the possible Fe3+-probe combination mechanism. Results: Apart from the probes' specific response toward Fe3+, the Fe3+-probe demonstrated highly quantitative relationships in fluorescence titration, instant labeling and dynamic tracking of intracellular Fe3+ in bioimaging. Conclusion: Cytotoxity and bioimaging in living L929 suggested the probes' future applications as real-time detection methods for Fe3+ in clinical diagnosis. Instant and time-lapse imagings, based on fluorescence-time stability of Fe3+-probe, enables the dynamic labeling and tracking of Fe3+ in living systems.
引用
收藏
页码:1859 / 1869
页数:11
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