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Manipulating the intramolecular motion of AIEgens for boosted biomedical applications

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  • ReceivedApr 1, 2019
  • AcceptedMay 6, 2019
  • PublishedMay 14, 2019

Abstract

There is no abstract available for this article.


Funded by

the NSFC(51622305,51873092)

the National Basic Research Program of China(2015CB856503)

and the Fundamental Research Funds for the Central Universities

Nankai University(63191521,63171218,63191176)


Acknowledgment

This work was supported by the National Natural Science Foundation of China (51622305, 51873092), the National Basic Research Program of China (2015CB856503), and the Fundamental Research Funds for the Central Universities, Nankai University (63191521, 63171218, 63191176).


Interest statement

The authors declare that they have no conflict of interest.


References

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  • Figure 1

    (a) Schematic illustration of the preparation of AIE dot with either corannulene-PEG or DSPE-PEG as the encapsulation matrix [10]; (b) schematic illustration of possible molecule arrangement of AIEgen and AIEgen-GFFY molecules in the aggregates [11] (color online).

  • Figure 2

    (a) Schematic illustrations of AIE and iMIPT mechanisms using their typical luminogens as the example; (b) PA tumor imaging (scale bar, 3 mm) of 4T1 tumor-bearing mice before (0 h) and after intravenous injection of iMIPT nanoparticles for different times [16] (color online).

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