Aceclofenac-loaded chitosan-tamarind seed polysaccharide interpenetrating polymeric network microparticles

Colloids Surf B Biointerfaces. 2013 May 1:105:303-9. doi: 10.1016/j.colsurfb.2013.01.013. Epub 2013 Jan 16.

Abstract

The present work deals with the preparation, characterization and evaluation of glutaraldehyde cross-linked chitosan-tamarind seed polysaccharide (TSP) interpenetrating polymeric network (IPN) microparticles for prolonged aceclofenac release. The drug entrapment efficiency of these microparticles was found 85.84±1.75 to 91.97±1.30% and their average particle sizes were ranged from 490.55±23.24 to 621.60±53.57 μm. These chitosan-TSP IPN microparticles were characterized by FTIR, DSC, and SEM analyses. The in vitro drug release from these aceclofenac-loaded chitosan-TSP IPN microparticles showed sustained release of aceclofenac over 8h and followed the Korsmeyer-Peppas model (R(2)=0.9809-0.9828) with anomalous (non-Fickian) diffusion drug release mechanism. The in vivo studies exhibited sustained anti-inflammatory activity in carrageenan-induced rats over prolonged period after oral administration of these newly developed aceclofenac-loaded IPN microparticles.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Calorimetry, Differential Scanning
  • Carrageenan / toxicity
  • Chitosan / chemistry*
  • Diclofenac / analogs & derivatives*
  • Diclofenac / pharmacology
  • Disease Models, Animal
  • Drug Delivery Systems
  • Edema / chemically induced
  • Edema / drug therapy*
  • Glutaral / metabolism
  • In Vitro Techniques
  • Male
  • Microspheres
  • Polymers / chemistry*
  • Polysaccharides / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Seeds / chemistry*
  • Spectroscopy, Fourier Transform Infrared
  • Tamarindus / chemistry*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Polymers
  • Polysaccharides
  • Diclofenac
  • Carrageenan
  • Chitosan
  • aceclofenac
  • Glutaral