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November 3, 2015Nature Communications940 citationsOpen Access

Perfluorocarbon nanoparticles enhance reactive oxygen levels and tumour growth inhibition in photodynamic therapy

YCYuhao ChengZhejiang Chinese Medical UniversityHCHao ChengChina Pharmaceutical UniversityCJChenxiao JiangUniversity of Science and Technology of China

Key Points

  • This research aims to develop an enhanced photodynamic therapy (Oxy-PDT) that alleviates hypoxia to improve cancer treatment efficacy.
  • Developed Oxy-PDT by loading a photosensitizer into perfluorocarbon nanodroplets.
  • Conducted in vivo studies with direct injection of Oxy-PDT into tumours in mice.
  • Compared effects of Oxy-PDT with traditional photodynamic therapy (PDT).
  • Oxy-PDT significantly increased the generation of reactive oxygen species (1)O2 and elevated cytotoxicity.
  • Mice treated with Oxy-PDT showed notable tumour growth inhibition after a single-dose intravenous injection.
  • Traditional PDT showed no effect on tumour growth compared to Oxy-PDT.

Abstract

Photodynamic therapy (PDT) kills cancer cells by converting tumour oxygen into reactive singlet oxygen ((1)O2) using a photosensitizer. However, pre-existing hypoxia in tumours and oxygen consumption during PDT can result in an inadequate oxygen supply, which in turn hampers photodynamic efficacy. Here to overcome this problem, we create oxygen self-enriching photodynamic therapy (Oxy-PDT) by loading a photosensitizer into perfluorocarbon nanodroplets. Because of the higher oxygen capacity and longer (1)O2 lifetime of perfluorocarbon, the photodynamic effect of the loaded photosensitizer is significantly enhanced, as demonstrated by the accelerated generation of (1)O2 and elevated cytotoxicity. Following direct injection into tumours, in vivo studies reveal tumour growth inhibition in the Oxy-PDT-treated mice. In addition, a single-dose intravenous injection of Oxy-PDT into tumour-bearing mice significantly inhibits tumour growth, whereas traditional PDT has no effect. Oxy-PDT may enable the enhancement of existing clinical PDT and future PDT design.

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Cite This Study

Cheng et al. (2015) studied this question.

synapsesocial.com/papers/69dd3aa9fb7610310c101320https://doi.org/10.1038/ncomms9785
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