Skip navigation

Continuous cocrystallization for dissolution rate optimization of a poorly water-soluble drug

Continuous cocrystallization for dissolution rate optimization of a poorly water-soluble drug

Moradiya, Hiren, Islam, Muhammad T., Woollam, Grahame R., Slipper, Ian J., Halsey, Sheelagh, Snowden, Martin J. ORCID: 0000-0002-1087-2692 and Douroumis, D. ORCID: 0000-0002-3782-0091 (2013) Continuous cocrystallization for dissolution rate optimization of a poorly water-soluble drug. Crystal Growth & Design, 14 (1). pp. 189-198. ISSN 1528-7483 (Print), 1528-7505 (Online) (doi:https://doi.org/10.1021/cg401375a)

Full text not available from this repository.

Abstract

A continuous manufacturing process, hot melt extrusion (HME), was employed for the development of high quality carbamazepine–saccharin (CBZ–SCH) cocrystals. The produced cocrystals were compared with a prototype prepared by a solvent method. It was found that processing parameters such as temperature, screw speed, and screw configuration were the critical processing parameters. In-line near-infrared analysis demonstrated that cocrystallization takes place gradually during the process along the extruder’s mixing zones. Further characterization of the extruded cocrystals proved that the manufactured highly crystalline cocrystals were similar to the prototype but had improved CBZ dissolution rates. Continuous manufacturing of cocrystals of water-insoluble drugs is a novel and robust approach.

Item Type: Article
Uncontrolled Keywords: polymorph spectroscopy
Subjects: Q Science > QD Chemistry
Faculty / School / Research Centre / Research Group: Faculty of Engineering & Science > School of Science (SCI)
Last Modified: 16 Apr 2020 13:26
URI: http://gala.gre.ac.uk/id/eprint/14422

Actions (login required)

View Item View Item