4.6 Article

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

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 3, Issue 36, Pages 7213-7221

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5tb01185j

Keywords

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Funding

  1. National Natural Science Foundation of China [51372003, 21271004, 51272001, 51472003, 51432001, 21271003]
  2. Ministry of Education Funded Projects Focus on returned overseas scholar
  3. Program for New Century Excellent Talents in University (China)
  4. Doctoral Program Foundation of Ministry of Education of China [20113401110004]
  5. China Postdoctoral Science Foundation [2015M571912]
  6. Swedish Research Council (VR) [621-2013-5357]
  7. Swedish Government strategic faculty grant in materials science (SFO, MATLIU) in Advanced Functional Materials (AFM)

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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.

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