4.8 Article

Organic semiconducting polymer amphiphile for near-infrared-II light-triggered phototheranostics

Journal

BIOMATERIALS
Volume 232, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2019.119684

Keywords

Semiconducting polymer; Amphiphile; Second near-infrared window; Photoacoustic imaging; Photothermal therapy

Funding

  1. National Natural Science Foundation of China [31570979]
  2. General Research Fund grant from the Research Grants Council of Hong Kong [14220716]
  3. Health and Medical Research Fund
  4. Food and Health Bureau
  5. Chow Yuk Ho Technology Centre for Innovative Medicine, The Chinese University of Hong Kong
  6. Shenzhen Science and Technology Innovation Commission Project [JCYJ20170307165611557]
  7. National Natural Science Foundation of China (NSFC) [81627805, 61805102]
  8. Research Grants Council of the Hong Kong Special Administrative Region [21205016, 11215817, 11101618]
  9. Shenzhen Basic Research Project [JCYJ20160329150236426, JCYJ20170413140519030]
  10. City University of Hong Kong [9667179]
  11. Government of the Hong Kong Special Administrative Region [04152836]

Ask authors/readers for more resources

Development of near-infrared-II (NIR-II) light responsive nano-agents with high photothermal stability, high photothermal conversion efficiency (PCE), and excellent biocompatibility for photoacoustic (PA) imaging-guided photothermal therapy (PIT) is of tremendous significance. In spite of the superiority of organic semiconducting polymer nanoparticles (OSPNs) in PA imaging-guided PIT, the limited absorption in the first NIR (NIR-I) window and metastable nanostructure of OSPNs resulting from commonly used preparation methods based on nanoprecipitation or reprecipitation compromise their in vivo phototheranostic performance. Herein we design and synthesize a novel NIR-II absorbing organic semiconducting polymer amphiphile (OSPA) to enhance the structural stability of OSPNs. With prominent optical properties, low toxicity, and a suitable size, OSPA not only efficiently labels and kills cancer cells under NIR-II irradiation but also accumulates at the tumor of living mice upon intravenous injection, allowing efficient NIR-II light-triggered phototheranostics toward tumor. The developed OSPA has promising potential for fabricating multifunctional nanoplatforms to enable multimodal theranostics.

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