4.8 Article

Triphenylamine flanked furan-diketopyrrolo-pyrrole for multi-imaging guided photothermal/photodynamic cancer therapy

Journal

NANOSCALE
Volume 9, Issue 47, Pages 18890-18896

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7nr07204j

Keywords

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Funding

  1. NNSF of China [61525402, 61775095, 21704043, 61371066]
  2. Jiangsu Provincial Key Research and Development Plan [BE2017741]
  3. State Key Laboratory of Materials-Oriented Chemical Engineering [KL15-06]
  4. Six Talent Peaks Project [51235018]
  5. Key University Science Research Project of Jiangsu Province [15KJA430006]
  6. Natural Science Foundation of Jiangsu Province [BK20170990, 17KJB150020]

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The combination of photodynamic therapy (PDT) and photothermal therapy (PTT) is highly desired to improve the cancer phototherapeutic effect. However, most reported multicomponent therapeutic agents need complex preparation processes and must be excited by using multiple light sources. Herein, triphenylamine flanked furan-diketopyrrolopyrrole (FDPP-TPA) with a donor-acceptor-donor structure has been synthesized and used as a sole-component agent for fluorescence, photoacoustic and photothermal imaging guided photodynamic and photothermal synergistic therapy. FDPP-TPA nanoparticles (NPs) obtained by re-precipitation exhibit a high molar extinction coefficient (epsilon = 2.13 (+/- 0.2) x 10(4) M-1 cm(-1)), excellent photothermal conversion efficiency (eta = 47%) and favorable singlet oxygen quantum yield (Phi(Delta(X)) = 40%). In vitro, the half-maximal inhibitory concentration (IC50) is 13 mu g mL(-1) determined by cytotoxicity assay. And the apoptosis rate is 67.3% according to flow cytometry analysis. In vivo, the tumor can be completely ablated without recurrence, which suggests that FDPP-TPA NPs can generate considerable poisonous singlet oxygen and hyperthermia for tumor treatment.

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