Topical nitric oxide releasing nanoparticles are effective in a murine model of dermal Trichophyton rubrum dermatophytosis

Nanomedicine. 2017 Oct;13(7):2267-2270. doi: 10.1016/j.nano.2017.06.018. Epub 2017 Jul 13.

Abstract

Systemic therapies are preferred for treating dermal dermatophytosis due to inadequate penetration of topical agents. However, systemic antifungals are associated with off-target effects and limited tissue penetration, and antimicrobial resistance is a growing concern. To address this, we investigated topical nitric oxide-releasing nanoparticles (NO-np), which have been used against superficial fungal infections and bacterial abscesses. In addition to enhanced penetration and permeation conferred by nanoparticles, nitric oxide, a broad-spectrum multi-mechanistic antimicrobial agent, offers decreased likelihood of resistance development. In the current study, NO-np inhibited Trichophyton rubrum in vitro, as well as in a murine model of dermal dermatophytosis. In mice, NO-np reduced fungal burden after three days, with complete clearance after seven. Furthermore, NO-np decreased tissue IL-2, 6, 10 and TNFα, indicating earlier attenuation of the host inflammatory response and decreased tissue morbidity. Thus, topical NO-np represent an attractive alternative to systemic therapy against dermal T. rubrum infection.

MeSH terms

  • Administration, Cutaneous
  • Animals
  • Antifungal Agents / administration & dosage
  • Antifungal Agents / therapeutic use*
  • Disease Models, Animal
  • Inflammation / complications
  • Inflammation / drug therapy
  • Inflammation / microbiology
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles / administration & dosage
  • Nanoparticles / therapeutic use*
  • Nitric Oxide / administration & dosage
  • Nitric Oxide / therapeutic use*
  • Tinea / complications
  • Tinea / drug therapy*
  • Tinea / microbiology
  • Trichophyton / drug effects*

Substances

  • Antifungal Agents
  • Nitric Oxide