A dual-emission fluorescent probe with independent polarity and viscosity responses: The synthesis, spectroscopy and bio-imaging applications

[Display omitted] •Independent dual-emission probe with polarity and viscosity responses.•Real-time imaging viscosity and polarity changes in living cells.•Dual-channel cancer cell discrimination.•NIR fluorescent (NIRF) imaging of rheumatoid arthritis in vivo. Viscosity and polarity are essential pa...

Full description

Saved in:
Bibliographic Details
Published inSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy Vol. 323; p. 124873
Main Authors Zhang, Ensheng, Zhang, Qingxiang, Wang, Shuping, Zhang, Guixue, Li, Anzhang, Lu, Wenhui, Ju, Ping
Format Journal Article
LanguageEnglish
Published England Elsevier B.V 15.12.2024
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:[Display omitted] •Independent dual-emission probe with polarity and viscosity responses.•Real-time imaging viscosity and polarity changes in living cells.•Dual-channel cancer cell discrimination.•NIR fluorescent (NIRF) imaging of rheumatoid arthritis in vivo. Viscosity and polarity are essential parameters that play critical roles in various physiological processes. Thus, dual-emission fluorescent probes that respond to both polarity and viscosity are highly sought-after tools for studying these processes. In addressing this need, a novel fluorescent probe (L), with dual emissions centered at 460 nm and 780 nm, which can sensitively respond to polarity and viscosity respectively, has been developed. Probe (L) is constructed through rational molecular design, utilizing two conjugated synthons connected by a π-bond to form a D-π-A system. The twisted intramolecular charge transfer (TICT) state is dominant in low-viscosity environments, resulting in weak near-infrared (NIR) fluorescence. Conversely, the intramolecular charge transfer (ICT) state is expected to prevail in high-viscosity environments, leading to strong NIR fluorescence. The polarity-sensitive fluorescence centered at 460 nm can be attributed to the emission of the coumarin unit. Moreover, probe (L) exhibits low cytotoxicity and primarily targets mitochondria. By leveraging the dual-emission properties of probe (L), real-time imaging of polarity and viscosity fluctuations within cells has been achieved. Additionally, probe (L) can be used for in situ and in vivo imaging of rheumatoid arthritis (RA) with good imaging resolution.
ISSN:1386-1425
1873-3557
DOI:10.1016/j.saa.2024.124873