Glutaryl Melatonin Niosome Gel for Topical Oral Mucositis: Anti- Inflammatory and Anticandidiasis

Curr Drug Deliv. 2020;17(3):195-206. doi: 10.2174/1567201817666200122162545.

Abstract

Background: Glutaryl melatonin, which is synthesized from melatonin and is a pineal glandderived neurohormone with anti-inflammatory and anti-oxidant properties, was comparatively investigated for its potential use as a topical anti-inflammatory agent.

Objective: Glutaryl melatonin, synthesized and screened for in vitro anti-candidiasis and in vitro and in vivo anti-inflammatory activities, was formulated as a niosome gel for topical oral evaluation in 5- fluorouracil-induced oral mucositis in mice.

Methods: In vitro anti-fungal activity in Candida albicans, in vitro anti-inflammatory activity in Escherichia coli liposaccharide-induced RAW cells and in vivo anti-inflammatory activity using a croton oilinduced ear edema model in ICR mice were investigated. Mucositis in mice (n= 6/group, 10-week-old mice) was induced by intraperitoneal injections of 5-fluorouracil, and the mice were subjected to a topical oral application of niosome gel containing melatonin (2% w/w) or glutaryl melatonin (2% w/w) and were compared with mice subjected to blank, fluocinolone acetonide (0.5% w/w) and control conditions.

Results: Glutaryl melatonin, at a 14.2 mM concentration, showed the highest fungicidal effect on C. albicans using the broth dilution method, indicating a nonsignificant difference from 1 μM of nystatin (p = 0.05). Nitric oxide, interleukin-6 and tumor necrosis factors were analyzed by ELISA. Liposaccharide-induced RAW cells were significantly reduced by glutaryl melatonin (p < 0.01). Ear edema inhibition of glutaryl melatonin was significant 1 h after application compared with that of melatonin (p = 0.03). Food consumption and body weight of the 5-fluorouracil-treated mice were significantly lower than those of the normal mice before all treatments (p < 0.05). Differences in the amount of licking behavior, which were observed in the control group for 5 min, were noticeable in the 5- fluorouracil-treated mice but not in the mice treated with the glutaryl melatonin niosome gel.

Conclusion: Glutaryl melatonin exhibited mild anti-candidiasis and anti-inflammatory properties. The incorporation of glutaryl melatonin in a niosome gel formulation, demonstrated the potential for topical oral applications to reduce oral discomfort caused by 5-fluorouracil treatment in mice.

Keywords: 5-fluorouracil; Glutaryl melatonin; anti-candidiasis; anti-inflammation; injections; niosome gel..

MeSH terms

  • Administration, Topical
  • Anhydrides / chemistry
  • Animals
  • Anti-Inflammatory Agents / administration & dosage*
  • Anti-Inflammatory Agents / chemistry
  • Antifungal Agents / administration & dosage*
  • Antifungal Agents / chemistry
  • Candida albicans / drug effects
  • Candida albicans / growth & development
  • Candidiasis / drug therapy*
  • Drug Liberation
  • Edema / drug therapy*
  • Fluorouracil
  • Gels
  • Glutarates / chemistry
  • Liposomes
  • Male
  • Melatonin / administration & dosage*
  • Melatonin / analogs & derivatives*
  • Melatonin / chemistry
  • Mice
  • Mice, Inbred ICR
  • RAW 264.7 Cells
  • Stomatitis / chemically induced
  • Stomatitis / drug therapy*

Substances

  • Anhydrides
  • Anti-Inflammatory Agents
  • Antifungal Agents
  • Gels
  • Glutarates
  • Liposomes
  • glutaric anhydride
  • Melatonin
  • Fluorouracil