Design and biological response of doxycycline loaded chitosan microparticles for periodontal disease treatment

Carbohydr Polym. 2018 Apr 15:186:260-272. doi: 10.1016/j.carbpol.2018.01.043. Epub 2018 Jan 31.

Abstract

The aim of this study was to develop chitosan (CS) microparticulated mucoadhesive drug delivery system (DDS) with improved therapeutic performance and biological responce. Ionotropic gelation/spray drying process was used for preparation of doxycycline hyclate (DOXY) loaded low and medium molecular weight (LMw and MMw) CS/sodium tripolyphosphate microparticles (CS/TPP MPs), further coated with ethyl cellulose (EC) using coacervation/solvent displacement technique. The relevant physico-chemical and biopharmaceutical properties were optimized using experimental design approach. Both coated and uncoated CS/TPP MPs showed high mucoadhesive potential and did not affect the viability of the tested epithelial cell line. The MPs induced slow and gradual apoptotic response in murine macrophage cell line RAW 264.7 and the observed effect depended upon formulation type and MP concentration. Biological effect of the CS-based MPs observed in our experiments point to synergism of the biological response of the carrier with the anti-inflammatory effect of DOXY.

Keywords: Chitosan/TPP microparticles; Doxycline hyclate; Mucoadhesive drug delivery system; Periodontal disease treatment.

MeSH terms

  • Animals
  • Cellulose / analogs & derivatives
  • Cellulose / chemistry
  • Chitosan / chemistry*
  • Doxycycline / chemistry*
  • Doxycycline / therapeutic use*
  • Drug Carriers / chemistry
  • Drug Delivery Systems / methods
  • Humans
  • Periodontal Diseases / drug therapy
  • Polyphosphates / chemistry

Substances

  • Drug Carriers
  • Polyphosphates
  • ethyl cellulose
  • Cellulose
  • Chitosan
  • Doxycycline
  • triphosphoric acid