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基于功能化十字桥联环番大环的阳离子双光子镧系元素发光生物探针。

Cationic Biphotonic Lanthanide Luminescent Bioprobes Based on Functionalized Cross-Bridged Cyclam Macrocycles.

机构信息

Univ Brest, UMR CNRS-UBO 6521 CEMCA, IBSAM, UFR des Sciences et Techniques, 6 Avenue Victor le Gorgeu, C.S. 93837, F-29238, Brest, Cedex 3, France.

Univ Lyon, ENS de Lyon, CNRS UMR 5182, Université Claude Bernard Lyon 1, F-69342, Lyon, France.

出版信息

Chemphyschem. 2020 May 18;21(10):1036-1043. doi: 10.1002/cphc.202000085. Epub 2020 Apr 7.

DOI:10.1002/cphc.202000085
PMID:32176399
Abstract

Cationic lanthanide complexes are generally able to spontaneously internalize into living cells. Following our previous works based on a diMe-cyclen framework, a second generation of cationic water-soluble lanthanide complexes based on a constrained cross-bridged cyclam macrocycle functionalized with donor-π-conjugated picolinate antennas was prepared with europium(III) and ytterbium(III). Their spectroscopic properties were thoroughly investigated in various solvents and rationalized with the help of DFT calculations. A significant improvement was observed in the case of the Eu complex, while the Yb analogue conserved photophysical properties in aqueous solvent. Two-photon (2P) microscopy imaging experiments on living T24 human cancer cells confirmed the spontaneous internalization of the probes and images with good signal-to-noise ratio were obtained in the classic NIR-to-visible configuration with the Eu luminescent bioprobe and in the NIR-to-NIR with the Yb one.

摘要

阳离子镧系元素配合物通常能够自发地进入活细胞。基于我们之前基于二亚甲基环已烷骨架的工作,用铕(III)和镱(III)合成了基于具有供体-π共轭吡啶甲酸酯天线的约束交叉桥联环已烷大环的第二代阳离子水溶性镧系元素配合物。在各种溶剂中彻底研究了它们的光谱性质,并借助 DFT 计算进行了合理化。Eu 配合物的观察到显著改善,而 Yb 类似物在水溶剂中保留了光物理性质。对活的 T24 人癌细胞的双光子(2P)显微镜成像实验证实了探针的自发内化,并且使用 Eu 发光生物探针在经典的近红外到可见配置中以及使用 Yb 在近红外到近红外配置中获得了具有良好信噪比的图像。

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