Novartis-MIT Center for Continuous Manufacturing, Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
J Pharm Sci. 2017 Nov;106(11):3328-3336. doi: 10.1016/j.xphs.2017.06.020. Epub 2017 Jul 4.
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.
热熔挤出和注塑(HME-IM)的组合是一种很有前途的连续制造片剂的工艺技术。然而,将其应用于制定含有晶型药物的速释片剂的研究还很有限。此外,应用 HME-IM 工艺于模制片剂的研究采用了非连续的 2 步方法。本研究采用集成的双螺杆 HME-IM 连续工艺,开发了基于麦芽糊精(MDX)的挤出模制速释片剂,用于一种晶型药物(灰黄霉素)。在 10%w/w 的药物载量下,根据初步筛选,选择 MDX 作为片剂基质形成剂。此外,还评估了液体和固体多元醇在 MDX 的熔融加工中的应用及其对片剂性能的影响。通过在与水平开口注塑机耦合的双螺杆挤出机上进行连续加工,生产出表面光滑的片剂,其包含结晶灰黄霉素固体悬浮在无定形 MDX-木糖醇基质中。实时 HME 工艺曲线用于开发自动化的 HME-IM 循环。通过配方调整克服了工艺挑战并提高了片剂的强度。所开发的 MDX 片剂表现出足够的强度和快速溶解的基质(20 分钟内 85%药物释放),并在加速稳定性条件下保持性能。