4.8 Article

Near-infrared light triggered photodynamic therapy in combination with gene therapy using upconversion nanoparticles for effective cancer cell killing

Journal

NANOSCALE
Volume 6, Issue 15, Pages 9198-9205

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4nr02495h

Keywords

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Funding

  1. National Basic Research Programs of China (973 Program) [2012CB932600, 2011CB911002]
  2. National Natural Science Foundation of China [81171394, 51302180, 81171392, 51222203]
  3. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
  4. Natural Science Foundation of Jiangsu Province [BK2011307]

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Upconversion nanoparticles (UCNPs) have drawn much attention in cancer imaging and therapy in recent years. Herein, we for the first time report the use of UCNPs with carefully engineered surface chemistry for combined photodynamic therapy (PDT) and gene therapy of cancer. In our system, positively charged NaGdF4:Yb,Er UCNPs with multilayered polymer coatings are synthesized via a layer by layer strategy, and then loaded simultaneously with Chlorin e6 (Ce6), a photosensitizing molecule, and small interfering RNA (siRNA), which targets the Plk1 oncogene. On the one hand, under excitation by a near-infrared (NIR) light at 980 nm, which shows greatly improved tissue penetration compared with visible light, cytotoxic singlet oxygen can be generated via resonance energy transfer from UCNPs to photosensitizer Ce6, while the residual upconversion luminescence is utilized for imaging. On the other hand, the silencing of Plk1 induced by siRNA delivered with UCNPs could induce significant cancer cell apoptosis. As the result of such combined photodynamic and gene therapy, a remarkably enhanced cancer cell killing effect is realized. Our work thus highlights the promise of UCNPs for imaging guided combination therapy of cancer.

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