Powder Characteristics of Proteins Spray-Dried from Different Spray-Dryers

喷雾干燥 休止角 酪蛋白 粒径 材料科学 粒度分布 粒子(生态学) 色谱法 堆积密度 化学工程 化学 复合材料 食品科学 环境科学 土壤水分 土壤科学 工程类 地质学 海洋学
作者
Todd P. Foster,Michael W. Leatherman
出处
期刊:Drug Development and Industrial Pharmacy [Taylor & Francis]
卷期号:21 (15): 1705-1723 被引量:22
标识
DOI:10.3109/03639049509069260
摘要

The powder characteristics of bovine somatotropin and casein spray-dried from laboratory, pilot and production spray-dryers were investigated. The powder characteristics examined included particle size distribution and morphology; bulk density; and flowability as measured by angle of repose, compressibility index and shear cell indices. Morphology classification showed internal voidage, blowholes, expanded, smooth and folding for somatotropin and casein spray-dried from the various spray-dryers. Particle size distributions of the bovine somatotropin and casein were unimodal and skewed. As the drying-chamber size of the spray-dryer increased, the particle sizes of both somatotropin and casein increased from mean volume diameters of 6-8 μ using the laboratory and pilot spray-dryers to 13-24 μ when using the production size spray-dryers. Spray-dried bovine somatotropin and casein had bulk densities of 0.090 to 0.195 g/cm3. Three flowability tests showed casein and somatotropin spray-dried from the different spray-dryers exhibited poor flow which could result in pharmaceutical manufacture challenges. The morphology and flowability of the two spray-dried proteins remained the same when comparing material produced from all four spray-dryers. However, the mean volume diameter, particle size distribution and bulk density did vary which might change critical product characteristics during scale-up. In general, similar morphology, particle size distributions, flowability and bulk densities were observed when comparing spray-dried casein and bovine somatotropin produced from the same model spray-dryer. Casein is recommended as a model protein for powder characterization during spray-drying and early formulation manufacture process development when adequate quantities of the recombinant protein are not available.
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