Polysaccharides based gastroretentive system to sustain piroxicam release: Development and in vivo prolonged anti-inflammatory effect

Int J Biol Macromol. 2018 Dec;120(Pt B):2303-2312. doi: 10.1016/j.ijbiomac.2018.08.140. Epub 2018 Aug 29.

Abstract

A gastro-retentive delivery system loaded with piroxicam with a bimodal release profile in gastrointestinal-tract was developed. Piroxicam is characterized by high oral absorption, long half-life, but its elimination is impaired in elderly patients. To overcome fluctuations in plasma levels, floating gastro-retentive gel-beads with sustained release properties were manufactured using prilling. Beads matrix was designed as a hollow/multipolymeric system based on alginate, ALM-pectin and hydroxypropilmethylcellulose. This research studied variables able to affect particles micromeritics, hollow inner structure, floating properties and drug-release profiles in gastro-intestinal tract. The gastro-retentive formulation (F4) acted as a floating-system able to provide the desired bimodal drug-release pattern controlling and delaying in vitro piroxicam release. The in vivo anti-inflammatory activity of the floating beads resulted prolonged up to 48 h, compared to standard piroxicam. This formulation may be proposed to treat chronic inflammatory-diseases in elderly patients, needing a rapid onset of drug action followed by a maintenance dose.

Keywords: Floating properties; Gastroretentive effect; Multipolymeric hollow beads; Piroxicam; in vitro sustained release; in vivo effectiveness.

MeSH terms

  • Alginates / chemistry*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry*
  • Anti-Inflammatory Agents, Non-Steroidal / metabolism*
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Delayed-Action Preparations
  • Drug Carriers / chemistry*
  • Drug Liberation
  • Gastric Mucosa / metabolism*
  • Male
  • Piroxicam / chemistry*
  • Piroxicam / metabolism*
  • Piroxicam / pharmacology
  • Rats
  • Rats, Wistar
  • Viscosity

Substances

  • Alginates
  • Anti-Inflammatory Agents, Non-Steroidal
  • Delayed-Action Preparations
  • Drug Carriers
  • Piroxicam