Solubility and dissolution studies of tibolone polymorphs
| Dublin Core | PKP Metadata Items | Metadata for this Document | |
| 1. | Title | Title of document | Solubility and dissolution studies of tibolone polymorphs |
| 2. | Creator | Author's name, affiliation, country | Rudy Bonfilio; Federal University of Alfenas; Faculty of Pharmaceutical Sciences; Department of Food and Medicines; Brazil |
| 2. | Creator | Author's name, affiliation, country | Marília Cristina Oliveira Souza; Federal University of Alfenas; Faculty of Pharmaceutical Sciences; Department of Food and Medicines; Brazil |
| 2. | Creator | Author's name, affiliation, country | Jockastta Silva Leal; Federal University of Alfenas; Faculty of Pharmaceutical Sciences; Department of Food and Medicines; Brazil |
| 2. | Creator | Author's name, affiliation, country | Olímpia Maria Martins Santos Viana; Federal University of Alfenas; Faculty of Pharmaceutical Sciences; Department of Food and Medicines; Brazil |
| 2. | Creator | Author's name, affiliation, country | Antônio Carlos Doriguetto; Federal University of Alfenas; Institute of Chemistry; Laboratory of Crystallography; Brazil |
| 2. | Creator | Author's name, affiliation, country | Magali Benjamin de Araújo; Federal University of Alfenas; Faculty of Pharmaceutical Sciences; Department of Food and Medicines; Brazil |
| 3. | Subject | Discipline(s) | |
| 3. | Subject | Keyword(s) | Tibolone/polymorphs; Powder X-ray diffraction/methods; Infrared spectroscopy/methods; Solubility/drug effects; Dissolution/analysis |
| 4. | Description | Abstract | Different solid forms of an active pharmaceutical ingredient can have distinct chemical and physical characteristics. In this work, we studied the solubility and dissolution properties of the described tibolone polymorphic forms (I and II). Both forms were successively recrystallized and characterized by powder X-ray diffraction and attenuated total reflection infrared spectroscopy. Equilibrium solubility and dissolution profiles were performed for both forms. Solubility studies demonstrated that form II is statistically more soluble in water, 0.01 mol L-1 HCl and pH 4.5 acetate buffer. The solubility of forms I and II were explained in terms of crystal packing. Dissolution tests of tablets showed a lower release of polymorphic form II than form I from tablets. The results showed an impact of polymorphism on the quality of tibolone tablets and suggest that tibolone forms I and II can show distinct interactions with pharmaceutical excipients used in tablets. Therefore, only form I is acceptable for the preparation of tablet forms. Based on our results, we propose the quality control on tibolone raw materials using X-ray diffraction analysis and attenuated total reflection infrared spectroscopy. |
| 5. | Publisher | Organizing agency, location | Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
| 6. | Contributor | Sponsor(s) | |
| 7. | Date | (YYYY-MM-DD) | 2017-01-01 |
| 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/144061 |
| 10. | Identifier | Digital Object Identifier (DOI) | http://dx.doi.org/10.1590/s2175-97902017000400233 |
| 11. | Source | Title; vol., no. (year) | Brazilian Journal of Pharmaceutical Sciences (Impresso); Vol 53, No 4 (2017) |
| 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) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso) This work is licensed under a Creative Commons Attribution 4.0 International License. |