Enteric coating of ibuprofen tablets (200 mg) using an aqueous dispersion system
| Dublin Core | PKP Metadata Items | Metadata for this Document | |
| 1. | Title | Title of document | Enteric coating of ibuprofen tablets (200 mg) using an aqueous dispersion system |
| 2. | Creator | Author's name, affiliation, country | Rabia Bushra; Ziauddin University; Ziauddin College of Pharmacy |
| 2. | Creator | Author's name, affiliation, country | Muhammad Harris Shoaib; University of Karachi; Faculty of Pharmacy; Department of Pharmaceutics |
| 2. | Creator | Author's name, affiliation, country | Nousheen Aslam; Ziauddin University; Ziauddin College of Pharmacy |
| 2. | Creator | Author's name, affiliation, country | Zafar Alam Mehmood; Colorcon Asia Pacific |
| 2. | Creator | Author's name, affiliation, country | Durriya Hashmat; University of Karachi; Faculty of Pharmacy; Department of Pharmaceutics |
| 3. | Subject | Discipline(s) | |
| 3. | Subject | Keyword(s) | Ibuprofen^i1^sadverse reacti;Tablets^i1^senteric coating/aqueous dispersion sys;Acryl-Eze. Opadry White;Superdisintegrant |
| 4. | Description | Abstract | Ibuprofen is a propionic acid derivative that belongs to the class NSAIDs. Major adverse reactions associated with Ibuprofen are related to GIT and include peptic and mucosal ulcers, dyspepsia, severe gastric pain and bleeding, that results in excessive treatment failure. The goal of this study was to develop enteric coated ibuprofen tablets in order to avoid gastric mucosal irritation, diffusion of drug across mucosal lining and to let active ingredient be absorbed easily in small intestine. The formulation was developed and manufactured through the direct compression process, the simplest, easiest and most economical method of manufacturing. Enteric coating was done using an Opadry white subcoating and an aqueous coating dispersion of Acryl-Eze. Enteric coated formulation was subjected to disintegration and dissolution tests by placing in 0.1 M hydrochloric acid for 2 h and then 1 h in phosphate buffer with a pH of 6.8. About 0.04% of drug was released in the acidic phase and 99.05% in the basic medium. These results reflect that ibuprofen can be successfully enteric coated in order to prevent its release in the stomach and facilitate rapid release of the drug in the duodenum, due to the presence of superdisintegrant. Formulating this enteric coated tablets could increase patient compliance by decreasing adverse drug reactions (ADR S) associated with Ibuprofen therapy. |
| 5. | Publisher | Organizing agency, location | Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
| 6. | Contributor | Sponsor(s) | |
| 7. | Date | (YYYY-MM-DD) | 2010-03-01 |
| 8. | Type | Status & genre | Peer-reviewed Article |
| 8. | Type | Type | |
| 9. | Format | File format | |
| 10. | Identifier | Uniform Resource Identifier | https://www.revistas.usp.br/bjps/article/view/10758 |
| 10. | Identifier | Digital Object Identifier (DOI) | http://dx.doi.org/10.1590/S1984-82502010000100011 |
| 11. | Source | Title; vol., no. (year) | Brazilian Journal of Pharmaceutical Sciences (Impresso); Vol 46, No 1 (2010) |
| 12. | Language | English=en | en |
| 13. | Relation | Supp. Files | |
| 14. | Coverage | Geo-spatial location, chronological period, research sample (gender, age, etc.) | |
| 15. | Rights | Copyright and permissions |
Copyright (c) 2017 Brazilian Journal of Pharmaceutical Sciences (Impresso)![]() This work is licensed under a Creative Commons Attribution 4.0 International License. |
