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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Simplified end-to-end continuous manufacturing by feeding API suspensions in twin-screw wet granulation
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Simplified end-to-end continuous manufacturing by feeding API suspensions in twin-screw wet granulation

机译:通过在双螺杆湿法造粒中喂食API悬浮液,简化了端到端连续制造

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摘要

This study focussed on investigating the coupling of continuous manufacturing of drug substance and continuous manufacture of drug product. An important step in such an integrated end-to-end continuous manufacturing was envisioned by dosing the API as suspension into a twin-screw wet granulation process. To achieve this goal, a model drug substance (ibuprofen) was fed as a concentrated aqueous suspension (50%?w/w) into a twin-screw granulator and compared against traditional solid feeding of the model drug substance to meet a target ibuprofen load of 60%?w/w in the formulation. Granulation and compaction behaviour were evaluated to determine the impact of feeding API as suspension in twin-screw wet granulation on the critical quality attributes of the drug product. It was demonstrated that the ibuprofen suspension feed is comparable with the ibuprofen dry blend feed in twin-screw wet granulation. Next to enabling end-to-end continuous manufacturing, API suspension feed in twin-screw wet granulation could afford a number of additional advantages including manufacturing efficiency by removing the drying step for API, or overcoming processing issues linked to the bulk properties of the API powder (e.g. flowability).
机译:本研究侧重于调查连续制造药物的偶联和连续制造药物产品。通过将API作为悬浮液将API作为悬浮在双螺杆湿造粒方法中,设想这种集成端到端连续制造中的一个重要步骤。为了实现这一目标,将模型药物(布洛芬)作为浓含水悬浮液(50%〜w / w)加入双螺杆造粒机中,并与模型药物的传统固体饲料进行比较,以满足靶布洛芬载荷在制剂中为60%?w / w。评估造粒和压实行为以确定饲料API在双螺杆湿造粒中的悬浮液对药品的临界质量属性的悬浮液。结果表明,布洛芬悬浮料与双螺杆湿法制粒中的布洛芬干混合物饲料相当。在实现端到端连续制造的旁边,双螺杆湿造粒中的API悬浮料可以提供许多额外的优点,包括通过去除API的干燥步骤,或克服与API的批量性质相关的处理问题粉末(例如流动性)。

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