Monitoring the Dissolution Mechanisms of Amorphous Bicalutamide Solid Dispersions via Real-Time Raman Mapping

Tres, Francesco; Aylott, Jonathan; Patient, Jamie D.; Williams, Philip M.; Treacher, Kevin; Booth, Jonathan; Hughes, Leslie P.; Wren, Stephen A.C.; Burley, Jonathan C.

Abstract

Real-time in situ Raman mapping has been employed to monitor, during dissolution, the crystallization transitions of amorphous bicalutamide formulated as a molecular dispersion in a copovidone VA64 matrix. The dissolution performance was also investigated using the rotating disc dissolution rate methodology, which allows simultaneous determination of the dissolution rate of both active ingredient and polymer. The dissolution behavior of two bicalutamide:copovidone VA64 dispersion formulations, containing 5% (w/w) and 50% (w/w) bicalutamide, respectively, was investigated, with the aim of exploring the effect of increasing the bicalutamide loading on the dissolution performance. Spatially time-resolved Raman maps generated using multivariate curve resolution indicated the simultaneous transformation of amorphous bicalutamide present in the 50% drug-loaded extrudate into metastable polymorphic form II and low-energy polymorphic form I. Fitting a kinetic model and spatially correlating the data extracted from the Raman maps also allowed us to understand the re-crystallization mechanisms by which the low-energy form I appears. Form I was shown to crystallize mainly directly from the amorphous solid dispersion, with crystallization from the metastable form II being a minor contribution.

Citation

Tres, F., Aylott, J., Patient, J. D., Williams, P. M., Treacher, K., Booth, J., Hughes, L. P., Wren, S. A., & Burley, J. C. (2015). Monitoring the Dissolution Mechanisms of Amorphous Bicalutamide Solid Dispersions via Real-Time Raman Mapping. Molecular Pharmaceutics, 12(5), 1512–1522. https://doi.org/10.1021/mp500829v

• Journal Article Type: Article
• Acceptance Date: Apr 15, 2015
• Publication Date: May 1, 2015
• Deposit Date: May 10, 2018
• Print ISSN: 1543-8384
• Publisher: American Chemical Society
• Peer Reviewed: Peer Reviewed
• Volume: 12
• Issue: 5
• Pages: 1512–1522
• DOI: https://doi.org/10.1021/mp500829v
• Public URL: https://nottingham-repository.worktribe.com/output/1107416
• Publisher URL: https://pubs.acs.org/doi/10.1021/mp500829v
• PMID: 00035407