Gastric ulcer healing by chebulinic acid solid dispersion-loaded gastroretentive raft systems: preclinical evidence

Author:

Negi Poonam1ORCID,Gautam Surbhi1,Sharma Aditi1,Rathore Charul1,Sharma Lalit1,Upadhyay Navneet1,Tambuwala Murtaza M2ORCID,Chellappan Dinesh Kumar3,Gupta Gaurav4ORCID,Prasher Parteek5ORCID,Dua Kamal678ORCID,Agarwal Shweta9ORCID,Lal Uma Ranjan10

Affiliation:

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. Centre for Inflammation, Centenary Institute, Royal Prince Alfred Hospital, Missenden Rd, Sydney NSW 2050

8. School of Biomedical Sciences & Pharmacy, The University of Newcastle, Callaghan, NSW 2308, Australia & Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute, Lot 1 Kookaburra Circuit, New Lambton Heights, Newcastle, NSW 2305, Australia

9. Department of Pharmaceutics, LR Institute of Pharmacy, Solan-173223, Himachal Pradesh, India

10. National Institute of Pharmaceutical Education & Research Ahmedabad, Pharmaceutical Sciences Ahmedabad, Gujarat, India

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.

Publisher

Future Science Ltd

Subject

Pharmaceutical Science

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