Management of recurrent aphthous ulcers exploiting polymer-based Muco-adhesive sponges : in-vitro and in-vivo evaluation

Drug Deliv. 2021 Dec;28(1):87-99. doi: 10.1080/10717544.2020.1858999.

Abstract

Recurrent aphthous ulcer (RAU) is a well-known painful, inflammatory disease with uncertain etiology for which local symptomatic therapy is only available. The aim of this study was to formulate and characterize muco-adhesive sponges containing a mixture of tenoxicam and miconazole nitrate to manage pain, inflammation and avoid candida infection that may accompany RAU due to poor oral hygiene. Two polymers at different concentrations were used to prepare sponges applying simple freeze-drying. Medicated chitosan (2%) sponges (mC2) showed acceptable physical appearance, surface pH (6.3 ± 0.042), porosity (25.7% ± 1.8), swelling index (5.7 ± 0.11), in-vivo and ex-vivo muco-adhesion time (115 min.±0.813 and 155 min.±1.537, respectively), ex-vivo muco-adhesion force (0.09 N ± 0.002) and scanning electron microscope (SEM) images. For concurrent clear-cut determination of tenoxicam and miconazole nitrate from mC2, a new UPLC method was developed and validated. mC2 sponges exhibited superior in-vitro drug release profiles where ∼100% of tenoxicam released within 5 min for fast pain relief with a more prolonged miconazole nitrate release. Furthermore, in-vivo animal study revealed that mC2 caused a significant decrease in the acetic acid-induced ulcer size in rats after 6 days of treatment (p < .0001) compared to negative and positive controls. Additionally, histopathological examination showed faster healing with complete restoration of the normal oral histology in rats. The present study concludes that chitosan sponge loaded with a combination of tenoxicam and miconazole nitrate could improve healing of RAU cases.

Keywords: CMC; Freeze-drying technique; chitosan; mucoadhesive buccal sponges; recurrent aphthous ulcer.

MeSH terms

  • Adhesives / administration & dosage
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage*
  • Antifungal Agents / administration & dosage*
  • Carboxymethylcellulose Sodium / chemistry
  • Chitosan / chemistry
  • Dose-Response Relationship, Drug
  • Drug Carriers / chemistry*
  • Drug Liberation
  • Freeze Drying
  • Hydrogen-Ion Concentration
  • Miconazole / administration & dosage*
  • Microscopy, Electron, Scanning
  • Piroxicam / administration & dosage
  • Piroxicam / analogs & derivatives*
  • Rats
  • Stomatitis, Aphthous / drug therapy*
  • Wound Healing

Substances

  • Adhesives
  • Anti-Inflammatory Agents, Non-Steroidal
  • Antifungal Agents
  • Drug Carriers
  • Piroxicam
  • Miconazole
  • Chitosan
  • Carboxymethylcellulose Sodium
  • tenoxicam

Supplementary concepts

  • Sutton disease 2