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Experimental Study of Fluidized Bed Co-Granulation of Two Active Pharmaceutical Ingredients: An Industrial Scale-Up Perspective

机译:两种活性药物成分在流化床中共制粒的实验研究:工业放大视角

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This article presents our efforts toward the development and scale-up of a fluidized bed process for co-granulation of two highly water-soluble active pharmaceutical ingredients (APIs) with a polymeric binder. The granulations were produced at three scales using Glatt GPCG3 (small), GPCG15 (pilot), and GPCG120 (commercial) fluid bed columns. The effects of binder concentration, atomization air pressure, and inlet air temperature were first investigated at the small scale. Based on the process knowledge generated at the small scale, various granulations were produced at the pilot scale to determine the effects of solution spray rate. We have demonstrated that, for a given binder solution, the droplet size distribution can be maintained similar by adjusting the atomization pressure when different spray rates were used upon scale-up. Superficial air velocity and moisture level in the powder bed appear to be the other key response parameters, which are, in turn, governed by various process and design parameters as well as formulation properties. This article demonstrates that the process and product quality remains invariant when the aforementioned key response variables are maintained during scale-up through some simple scale-up rules.
机译:本文介绍了我们为流化床工艺的发展和规模所做的努力,以使两种高度水溶性的活性药物成分(API)与聚合物粘合剂共同造粒。使用Glatt GPCG3(小型),GPCG15(中试)和GPCG120(商业)流化床色谱柱以三种规模生产颗粒。首先以小规模研究了粘合剂浓度,雾化气压和进气温度的影响。根据小规模生产的工艺知识,以中试规模生产各种颗粒,以确定溶液喷雾速率的影响。我们已经证明,对于给定的粘合剂溶液,当按比例放大时使用不同的喷雾速率时,可以通过调节雾化压力来保持液滴尺寸分布相似。粉末床中的表面空气速度和湿度水平似乎是其他关键响应参数,而这些参数又由各种工艺和设计参数以及配方特性决定。本文演示了通过一些简单的放大规则在放大过程中保持上述关键响应变量时,过程和产品质量仍然保持不变。

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