| Literature DB >> 28684263 |
Vibha Puri1, Dave Brancazio1, Parind M Desai1, Keith D Jensen1, Jung-Hoon Chun2, Allan S Myerson1, Bernhardt L Trout3.
Abstract
The combination of hot-melt extrusion and injection molding (HME-IM) is a promising process technology for continuous manufacturing of tablets. However, there has been limited research on its application to formulate crystalline drug-containing immediate-release tablets. Furthermore, studies that have applied the HME-IM process to molded tablets have used a noncontinuous 2-step approach. The present study develops maltodextrin (MDX)-based extrusion-molded immediate-release tablets for a crystalline drug (griseofulvin) using an integrated twin-screw HME-IM continuous process. At 10% w/w drug loading, MDX was selected as the tablet matrix former based on a preliminary screen. Furthermore, liquid and solid polyols were evaluated for melt processing of MDX and for impact on tablet performance. Smooth-surfaced tablets, comprising crystalline griseofulvin solid suspension in the amorphous MDX-xylitol matrix, were produced by a continuous process on a twin-screw extruder coupled to a horizontally opening IM machine. Real-time HME process profiles were used to develop automated HME-IM cycles. Formulation adjustments overcame process challenges and improved tablet strength. The developed MDX tablets exhibited adequate strength and a fast-dissolving matrix (85% drug release in 20 min), and maintained performance on accelerated stability conditions.Entities:
Keywords: continuous manufacturing; crystalline solid suspension; griseofulvin; hot-melt extrusion; immediate release; injection molding; maltodextrin
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Year: 2017 PMID: 28684263 DOI: 10.1016/j.xphs.2017.06.020
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534