4.8 Article

Graphene nanoribbon-based supramolecular ensembles with dual-receptor targeting function for targeted photothermal tumor therapy

Journal

CHEMICAL SCIENCE
Volume 12, Issue 33, Pages 11089-11097

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1sc02154k

Keywords

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Funding

  1. National Natural Science Foundation of China [21788102, 91853201, 21774076, 21776078]
  2. National Key Sci-Tech Special Projects of Infection Diseases of China [2018ZX10732202]
  3. Shanghai Municipal Science and Technology Major Project [2018SHZDZX03]
  4. International Cooperation Program of Shanghai Science and Technology Committee [17520750100]
  5. Program of Shanghai Academic Research Leader [19XD1421700]
  6. Fundamental Research Funds for the Central Universities [222201717003]
  7. National Postdoctoral Program for Innovative Talents [BX20190115]
  8. Shanghai Post-doctoral Excellence Program [2019044]
  9. China Postdoctoral Science Foundation [2020M681206]
  10. Royal Society
  11. Open Research Fund of the School of Chemistry and Chemical Engineering, Henan Normal University [2020ZD01]

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A supramolecular ensemble, GNR-Man/PRGD, based on graphene nanoribbons was constructed for targeted photothermal treatment of TNBC, demonstrating enhanced therapeutic efficacy compared to non-targeting equivalents in both in vitro and in vivo studies. The platform holds promise for the development of photothermal nanomaterials for targeted tumor therapy.
Triple negative breast cancer (TNBC) is one of the most malignant subtypes of breast cancer. Here, we report the construction of graphene nanoribbon (GNR)-based supramolecular ensembles with dual-receptor (mannose and alpha(v)beta(3) integrin receptors) targeting function, denoted as GNR-Man/PRGD, for targeted photothermal treatment (PTT) of TNBC. The GNR-Man/PRGD ensembles were constructed through the solution-based self-assembly of mannose-grafted GNRs (GNR-Man) with a pyrene-tagged alpha(v)beta(3) integrin ligand (PRGD). Enhanced PTT efficacies were achieved both in vitro and in vivo compared to that of the non-targeting equivalents. Tumor-bearing live mice were administered (tail vein) with GNR-Man/PRGD and then each mice group was subjected to PTT. Remarkably, GNR-Man/PRGD induced complete ablation of the solid tumors, and no tumor regrowth was observed over a period of 15 days. This study demonstrates a new and promising platform for the development of photothermal nanomaterials for targeted tumor therapy.

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