Mechanistic study of tumor fluorescence response signals based on a near-infrared viscosity-sensitive probe

  • 0Joint Laboratory of Opto-Functional Theranostics in Medicine and Chemistry, First Hospital of Jilin University, Changchun 130021, P. R. China. zhangyueweichem@163.com.

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Summary

This summary is machine-generated.

This study introduces a new near-infrared fluorescence probe for measuring viscosity. The research reveals that cellular state, not the tumor microenvironment, primarily influences probe signals, advancing viscosity probe applications.

Area Of Science

  • Biomedical Engineering
  • Chemical Biology
  • Molecular Imaging

Background

  • Viscosity is a key physiological parameter linked to cellular functions and diseases.
  • Existing viscosity-sensitive fluorescence probes show promise for tumor imaging but lack mechanistic clarity due to environmental interference.

Purpose Of The Study

  • To develop and characterize a novel viscosity-responsive fluorescence probe.
  • To elucidate the primary mechanism driving fluorescence changes in viscosity probes within complex biological systems.

Main Methods

  • Development of a near-infrared (700-1200 nm) fluorescence probe utilizing the twisted intramolecular charge transfer (TICT) mechanism.
  • Evaluation of probe photostability and dual targeting of mitochondria and lysosomes.
  • In-depth analysis to differentiate contributions of cellular state, tumor microenvironment, and cell type to probe response.

Main Results

  • The developed probe exhibits an ultra-wide emission range in the near-infrared spectrum with strong photostability.
  • The probe successfully targets both mitochondria and lysosomes.
  • Cellular intrinsic state was identified as the dominant factor influencing probe fluorescence changes, outweighing microenvironmental or cell-type effects.

Conclusions

  • The developed TICT-based probe offers a robust tool for viscosity sensing with advanced spectral properties and organelle targeting.
  • Understanding the primary role of cellular state provides crucial theoretical insights for the rational design and application of future viscosity-responsive probes in biomedical research.