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Area of Science:

  • Biomedical Engineering
  • Molecular Imaging
  • Nanotechnology

Background:

  • Activatable molecular probes are crucial for targeted cancer imaging.
  • Hydrophobic probes often aggregate in aqueous media, hindering their responsiveness and practical application.

Purpose of the Study:

  • To develop novel small molecular probes with enhanced responsiveness to hydrogen sulfide (H₂S) for in vivo imaging of H₂S-rich cancers.
  • To address the aggregation issue of conventional probes in aqueous environments.

Main Methods:

  • Designed two small molecular probes by modulating hydrophilicity-lipophilicity balance using N-methylpyridinium.
  • Investigated the spontaneous self-assembly into nanoprobes under physiological conditions.
  • Evaluated probe performance for near-infrared fluorescence and photoacoustic signal generation upon H₂S activation.

Main Results:

  • The designed probes spontaneously self-assemble into nanoprobes in physiological conditions.
  • Aggregated probes exhibit enhanced near-infrared fluorescence and photoacoustic signals upon specific H₂S activation.
  • Enabled in vivo visualization and differentiation of cancers based on H₂S content.

Conclusions:

  • Developed a novel design strategy for activatable molecular probes with aggregation-enhanced responsiveness.
  • Demonstrated the potential for in vivo imaging and precision cancer diagnostics using H₂S-responsive nanoprobes.
  • The strategy paves the way for optimized probe design for improved cancer detection.