Evolution of Nanoparticle-Mediated Photodynamic Therapy: From Superficial to Deep-Seated Cancers

Molecules. 2019 Jan 31;24(3):520. doi: 10.3390/molecules24030520.

Abstract

Enthusiasm for photodynamic therapy (PDT) as a potential therapeutic intervention for cancer has increased exponentially in recent decades. Photodynamic therapy constitutes a clinically approved, minimally invasive treatment modality that uses a photosensitizer (light absorbing molecule) and light to kill cancer cells. The principle of PDT is, when irradiated with a light of a suitable wavelength, a photosensitizer absorbs the light energy and generates cytotoxic free radicals through various mechanisms. The overall efficiency of PDT depends on characteristics of activation light and in-situ dosimetry, including the choice of photosensitizer molecule, wavelength of the light, and tumor location and microenvironment, for instance, the use of two-photon laser or an X-ray irradiator as the light source increases tissue-penetration depth, enabling it to achieve deep PDT. In this mini-review, we discuss the various designs and strategies for single, two-photon, and X-ray-mediated PDT for improved clinical outcomes.

Keywords: PDT; X-ray; photodynamic therapy; photosensitizer; single-photon; two-photon.

Publication types

  • Review

MeSH terms

  • Animals
  • Drug Compounding
  • Humans
  • Light
  • Nanoparticles* / chemistry
  • Neoplasms / pathology
  • Neoplasms / therapy
  • Photochemotherapy* / methods
  • Photons
  • Photosensitizing Agents* / chemistry
  • X-Rays

Substances

  • Photosensitizing Agents