Gelatin-carboxymethyl tamarind gum biocomposites: In vitro characterization & anti-inflammatory pharmacodynamics

Mater Sci Eng C Mater Biol Appl. 2016 Dec 1:69:478-85. doi: 10.1016/j.msec.2016.07.008. Epub 2016 Jul 5.

Abstract

In this study, gelatin and carboxymethyl tamarind gum (CTG) were chemically cross-linked to control the delivery of aceclofenac from their interpenetrating network (IPNs). Infrared spectra, thermal and X-ray data supported that drug and polymer was compatible in the composite hydrogels. Irregularly shaped IPN microstructures were seen under field emission scanning electron microscope (FE-SEM). IPN system was capable of entrapping about 96% of the drug fed. CTG in IPN structures suppressed the drug release rate in HCl solution (pH1.2); however extended the same in phosphate buffer solution (pH6.8). The drug release was controlled by polymer chain relaxation/swelling and simple diffusion in vitro. The anti-inflammatory activity of drug-loaded biocomposites lasted over 7h in albino rats, thus suggesting their potential as an anti-inflammatory therapeutics.

Keywords: Anti-inflammatory activity; Biocomposites; Gelatin; Interpenetrating network; Tamarind polysaccharide.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / administration & dosage
  • Anti-Inflammatory Agents / chemistry*
  • Anti-Inflammatory Agents / metabolism
  • Calorimetry, Differential Scanning
  • Diclofenac / administration & dosage
  • Diclofenac / analogs & derivatives
  • Diclofenac / chemistry
  • Diclofenac / metabolism
  • Disease Models, Animal
  • Drug Carriers / chemistry*
  • Drug Liberation
  • Edema / chemically induced
  • Edema / drug therapy
  • Female
  • Gelatin / chemistry*
  • Hydrogels / chemistry
  • Male
  • Microscopy, Electron, Scanning
  • Polysaccharides / chemistry*
  • Rats
  • Spectroscopy, Fourier Transform Infrared
  • Tamarindus / metabolism*

Substances

  • Anti-Inflammatory Agents
  • Drug Carriers
  • Hydrogels
  • Polysaccharides
  • Diclofenac
  • Gelatin
  • aceclofenac