4.8 Article

Exploiting Single Atom Iron Centers in a Porphyrin-like MOF for Efficient Cancer Phototherapy

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 38, Pages 35228-35237

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b11238

Keywords

single atom catalysts; porphyrin; MOFs; photothermal therapies; photoacoustic

Funding

  1. National Natural Science Foundation of China [21805293, 21627813]
  2. Fundamental Research Funds for the Central Universities [XK1802-6]
  3. Director Foundation of the Technical Institute of Physics and Chemistry, Chinese Academy of Sciences [2018-GSY]
  4. Youth Innovation Promotion Association of Chinese Academy of Sciences [2019027]
  5. Dodd Walls Centre for Photonic and Quantum Technologies
  6. MacDiarmid Institute for Advanced Materials and Nanotechnology
  7. Ministry of Business Innovation and Employment (MBIE) Catalyst Fund [MAUX1609]

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In recent years, single-atom catalysts (SACs) have attracted enormous attention due their effectiveness in promoting a variety of catalytic reactions. However, the ability of SACs to enhance cancer phototherapies has received little attention to date. Herein, we synthesized a metal organic framework (MOF) rich in porphyrin-like single atom Fe(III) centers (denoted herein as porphyrin-MOF or P-MOF) and then evaluated the performance of the P-MOF for cancer treatment by photodynamic therapy (PDT) and photothermal therapy (PTT) under NIR (808 nm) irradiation, as well as photoacoustic imaging (PM) of tumors. On acccount of the abundance of single atom Fe(III) centers, the P-MOF material demonstrated excellent performance for modulation of the hypoxic tumor microenvironment of Hela cell tumors in mice, while also demonstrating good properties as a photoacoustic imaging (PAI) agent. Density functional theory (DFT) calculations were used to elucidate the superior performance of P-MOF in these applications relative to Fe2O3 (a Fe(III) reference compound). The calculations revealed that the narrow band gap energy of P-MOF (1.31 eV) enabled strong absorption of NIR photons, thereby inducing nonradiative transitions that converted incident light into heat to promote PTT. Further, a facile change of the spin state of the single atom Fe(III) centers in P-MOF under NIR irradiation transformed coordinated triplet oxygen (O-3(2)) to singlet oxygen (O-1(2)), benefiting PDT. This work demonstrates the great future potential of both SACs and MOFs as multifunctional agents for cancer treatment and tumor imaging.

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