Quinoidal π-Bridges for a Fused-Ring Acceptor with Enhanced Near-Infrared-II Photothermal Therapy and Fluorescent Emission beyond 1500 nm

  • Wuke Cao
  • , Xun Zhang
  • , Xueqin Yang
  • , Haitao Sun*
  • , Zhongxin Chen*
  • , Yongye Liang*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

The second near-infrared window (NIR-II, 1000-3000 nm) presents an attractive platform for phototheranostics due to improved tissue penetration. However, developing efficient phototheranostic agents for this range presents a significant challenge. Herein, we report an NIR-II organic theranostic agent, CNTIC-4F, based on a fused-ring acceptor structure, which features efficient absorption extending beyond 1200 nm and fluorescence emission reaching up to 1800 nm. The incorporation of a proaromatic π-bridge, thieno[3,4-b]pyrazine (TP), enhances the quinoidal character of CNTIC-4F, reducing the optical bandgap and enhancing intermolecular interactions. In vivo fluorescence imaging of mouse vasculature with CNTIC-4F nanoparticles shows high-contrast imaging beyond 1500 nm under 1064 nm excitation. Furthermore, CNTIC-4F nanoparticles also exhibit a high photothermal conversion efficiency of 82% under 1064 nm excitation, enabling effective NIR-II imaging-guided photothermal therapy of 4T1 tumors in mice. This study illustrates the potential of quinoidal structures in developing advanced organic agents for high-contrast and deep-penetrating NIR-II phototheranostics.

Original languageEnglish
Pages (from-to)2687-2695
Number of pages9
JournalACS Materials Letters
Volume6
Issue number7
DOIs
StatePublished - 1 Jul 2024
Externally publishedYes

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