Antimicrobial photodynamic therapy using chlorin e6 with halogen light for acne bacteria-induced inflammation

Life Sci. 2015 Mar 1:124:56-63. doi: 10.1016/j.lfs.2014.12.029. Epub 2015 Jan 23.

Abstract

Aims: The present study was designed to evaluate the therapeutic potential of antimicrobial photodynamic therapy (PDT) using chlorin e6 with halogen light against acne bacteria-induced inflammation.

Main methods: Highly purified chlorin e6 (Ce6), as a second generation photosensitizer, was synthesized from Spirulina chlorophyll. To evaluate the antimicrobial property of Ce6-mediated PDT with halogen light, the broth microdilution method and two-color fluorescence assay were used. The free radicals generated upon irradiating Ce6 with halogen light were measured using 2,7-dichlorofluorescin diacetate. Propionibacterium acnes was intradermally injected into the left ear of the ICR mice, and the anti-inflammatory effect of Ce6-mediated PDT with halogen light was measured by the histological examination. The expressions of cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS) as well as pro-inflammatory cytokines were also measured by Western blotting.

Key findings: Chlorin e6-mediated PDT with halogen light (30,000 lx) inactivated various skin bacteria, including P. acnes in a dose-dependent manner. The MIC99 value against P. acnes (KCTC3314) of Ce6 with light was >0.49 μg/ml, whereas the MIC99 for Ce6 alone was >31.25 μg/ml. Ce6-mediated PDT suppressed the expression of P. acnes-induced pro-inflammatory cytokines and iNOS, but not COX-2 in a mouse model.

Significance: This study showed a remarkable therapeutic effect of chlorin e6-mediated PDT with halogen light against P. acnes-induced inflammation. Our results suggest for the first time the potential of Ce6-mediated PDT with halogen light as a more effective and safer alternative treatment to antibiotic therapy against pathogenic infections of the skin.

Keywords: Anti-inflammatory effect; Anti-microbial effect; Chlorin e6; Halogen light; Photodynamic therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acne Vulgaris / drug therapy*
  • Acne Vulgaris / microbiology
  • Animals
  • Blotting, Western
  • Chlorophyllides
  • Cyclooxygenase 2 / genetics
  • Cytokines / genetics
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation
  • Halogens
  • Inflammation / drug therapy*
  • Inflammation / microbiology
  • Male
  • Mice
  • Mice, Inbred ICR
  • Nitric Oxide Synthase Type II / genetics
  • Photochemotherapy / adverse effects
  • Photochemotherapy / methods*
  • Porphyrins / administration & dosage*
  • Propionibacterium acnes / drug effects*
  • Radiation-Sensitizing Agents / administration & dosage

Substances

  • Chlorophyllides
  • Cytokines
  • Halogens
  • Porphyrins
  • Radiation-Sensitizing Agents
  • phytochlorin
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2