Affiliations 

  • 1 School of Pharmaceutical Sciences, Shoolini University of Biotechnology & Management Sciences, Solan-173 212, Himachal Pradesh, India
  • 2 School of Pharmacy & Pharmaceutical Sciences, Ulster University, Coleraine, County Londonderry, BT52 1SA, Northern Ireland, UK
  • 3 Department of Life Sciences, School of Pharmacy, International Medical University, Bukit Jalil 57000, Kuala Lumpur, Malaysia
  • 4 School of Pharmacy, Suresh Gyan Vihar University, Jagatpura 302017, Mahal Road, Jaipur, India
  • 5 Department of Chemistry, University of Petroleum & Energy Studies, Dehradun 248007, India
  • 6 Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Ultimo NSW 2007, Australia
  • 7 Department of Pharmaceutics, LR Institute of Pharmacy, Solan-173223, Himachal Pradesh, India
  • 8 National Institute of Pharmaceutical Education & Research Ahmedabad, Pharmaceutical Sciences Ahmedabad, Gujarat, India
Ther Deliv, 2022 Feb;13(2):81-93.
PMID: 35075915 DOI: 10.4155/tde-2021-0062

Abstract

Background: Chebulinic acid (CA), a component in Terminalia chebula, exhibits antiulcer activity, but has poor aqueous solubility. Raft-forming systems incorporating solid dispersions (SDs) of CA, were developed to overcome its poor biopharmaceutical properties and to prolong the gastric residence time for maximum activity. Methods: SDs were formulated by a solvent evaporation method using Eudragit EPO. Raft formulations consisted of sodium alginate as a polymer. Results: Release of CA in the dissolution medium was 40%, whereas SDs showed 95.45% release. The CA raft system (20 mg/kg) showed curative efficacy in an alcohol-induced gastric ulcer model and increased protection when compared with omeprazole (10 mg/kg) and CA suspension (20 mg/kg). Conclusion: These studies demonstrated SD raft systems to be a promising approach for antiulcer therapy by CA.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.