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Endoplasmic Reticulum-Targeting Delayed Fluorescent Probe for Dual-mode Nitroreductase Sensing.

V T K Shradha1, Subhadeep Das1, Abhijit Patra1

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Summary

New organic probes enable sensitive, dual-mode detection of cancer biomarkers. These probes utilize delayed fluorescence for specific imaging in cancer cells, overcoming limitations of existing materials.

Keywords:
Endoplasmic reticulumFluorescence imagingNitroreductase sensingThermally activated delayed fluorescenceTime-resolved fluorescence imaging

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Area of Science:

  • Organic chemistry
  • Biomedical imaging
  • Cancer biomarker detection

Background:

  • Organic thermally activated delayed fluorescence (TADF) materials offer long-lived emission for time-resolved imaging.
  • Challenges include air sensitivity, lack of organelle specificity, and limited analyte recognition for cancer biomarkers like nitroreductase (NTR).

Purpose of the Study:

  • To develop novel donor-acceptor based probes for specific and sensitive detection of cancer biomarkers.
  • To overcome limitations of existing TADF materials for biological applications.

Main Methods:

  • Synthesis of triphenylamine-quinoxaline based probes (TPQS and TPNS) functionalized with a sulphonamide unit.
  • Utilizing time-resolved fluorescence measurements to confirm delayed fluorescence properties.
  • Developing a nitroreductase (NTR) specific probe (TPNS) with a "turn-on" luminescence mechanism.

Main Results:

  • TPQS probe exhibits delayed fluorescence due to a minimal singlet-triplet energy gap.
  • TPNS probe shows "turn-on" luminescence and delayed fluorescence upon reaction with NTR.
  • Dual-mode detection of NTR achieved in cancer cells using confocal and time-resolved fluorescence imaging (TRFI).

Conclusions:

  • Developed probes demonstrate potential for sensitive and specific detection of cancer biomarkers.
  • Delayed fluorescent emitters show promise for advanced bioimaging in complex biological systems.
  • Functionalized probes offer endoplasmic reticulum specificity and precise analyte recognition.