A series of Zn(II) terpyridine complexes with enhanced two-photon-excited fluorescence for in vitro and in vivo bioimaging

被引:37
|
作者
Zhang, Qiong [1 ,2 ]
Tian, Xiaohe [3 ]
Hu, Zhangjun [2 ]
Brommesson, Caroline [2 ]
Wu, Jieying [1 ]
Zhou, Hongping [1 ]
Li, Shengli [1 ]
Yang, Jiaxiang [1 ]
Sun, Zhaoqi [4 ]
Tian, Yupeng [1 ,5 ]
Uvdal, Kajsa [2 ]
机构
[1] Anhui Univ, Dept Chem, Key Lab Funct Inorgan Mat Chem Anhui Prov, Hefei 230039, Peoples R China
[2] Linkoping Univ, Div Mol Surface Phys & Nanosci, Dept Phys Chem & Biol IFM, S-58183 Linkoping, Sweden
[3] UCL, Dept Chem, MRC UCL Ctr Med Mol Virol, London WC1H 0AJ, England
[4] Anhui Univ, Sch Phys & Mat Sci, Hefei 230601, Peoples R China
[5] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 250100, Jiangsu, Peoples R China
基金
瑞典研究理事会; 中国博士后科学基金; 中国国家自然科学基金;
关键词
INTRAMOLECULAR CHARGE-TRANSFER; PHOTOPHYSICAL PROPERTIES; 2,2'/6',2''-TERPYRIDINE-BASED LIGAND; ONE-PHOTON; ABSORPTION; PROBES; CHROMOPHORES; MICROSCOPY; WATER; CELL;
D O I
10.1039/c5tb01185j
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
It is still a challenge to obtain two-photon excited fluorescent bioimaging probes with intense emission, high photo-stability and low cytotoxicity. In the present work, four Zn(II)-coordinated complexes (1-4) constructed from two novel D-A and D-p-A ligands (L-1 and L-2) are investigated both experimentally and theoretically, aiming to explore efficient two-photon probes for bioimaging. Molecular geometry optimization used for theoretical calculations is achieved using the crystallographic data. Notably, the results indicate that complexes 1 and 2 display enhanced two-photon absorption (2PA) cross sections compared to their corresponding D-A ligand (L1). Furthermore, it was found that complex 1 has the advantages of moderate 2PA cross section in the near-infrared region, longer fluorescence lifetime, higher quantum yield, good biocompatibility and enhanced two-photon excited fluorescence. Therefore, complex 1 is evaluated as a bioimaging probe for in vitro imaging of HepG2 cells, in which it is observed under a two-photon scanning microscope that complex 1 exhibits effective co-staining with endoplasmic reticulum (ER) and nuclear membrane; as well as for in vivo imaging of zebrafish larva, in which it is observed that complex 1 exhibits specificity in the intestinal system.
引用
收藏
页码:7213 / 7221
页数:9
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