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Multi-level macrocyclic assembly achieving organic upconversion delayed fluorescence for targeted cell imaging.

Jie Niu1, Xuan Wu2, Jie Yu3

  • 1Medical College, Department of Basic Medicine and Medical Technology, Yangzhou University Yangzhou Jiangsu 225009 China.

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|September 22, 2025
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Summary
This summary is machine-generated.

Researchers developed a novel supramolecular assembly for enhanced deep-red luminescence. This purely organic upconversion phosphor system, utilizing macrocyclic confinement, shows promise for advanced targeted cell imaging applications.

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Area of Science:

  • Supramolecular Chemistry
  • Organic Materials Science
  • Bioimaging Technologies

Background:

  • Purely organic room-temperature phosphorescence (PORTP) materials are valuable for bioimaging.
  • Existing PORTP materials often have short excitation wavelengths, limiting their applications.
  • Developing long-lived, deep-red emitting organic materials is crucial for advanced imaging.

Purpose of the Study:

  • To engineer a novel purely organic phosphorescence resonance energy transfer (PRET) assembly.
  • To achieve enhanced PORTP and multi-photon-mediated PRET for delayed deep-red luminescence.
  • To demonstrate the utility of this assembly for targeted cell imaging.

Main Methods:

  • Construction of a supramolecular assembly using 6-bromoisoquinolium-modified permethylated β-cyclodextrin (BQ-PCD), cucurbit[8]uril (CB[8]), and tetra(4-sulfonatophenyl)porphyrin (TPPS).
  • Utilizing macrocyclic confinement (CB[8]) to enhance PORTP lifetime.
  • Employing multi-photon excitation and phosphorescence resonance energy transfer (PRET) for deep-red emission.
  • Assembling with hyaluronic acid (HA) for tumor-targeting capabilities.

Main Results:

  • The BQ-PCD⊂CB[8] assembly significantly prolonged PORTP lifetime (13.8 ns to 640 μs).
  • The TPPS⊂BQ-PCD⊂CB[8] system achieved efficient PRET (94.5%) yielding delayed deep-red luminescence (around 11 μs lifetime).
  • Multi-photon excitation at 920 nm enabled deep-red emission via the upconversion process.
  • The HA-conjugated nanoparticle demonstrated successful targeted cell imaging.

Conclusions:

  • Macrocyclic confinement effectively enhances PORTP and enables efficient PRET.
  • The developed upconversion supramolecular nanoparticle provides a novel platform for long-lived, deep-red emission.
  • This approach offers a promising strategy for advanced targeted cell imaging.