Varca Gustavo H C, Lopes Patricia S, Ferraz Humberto G
Departamento de Farmácia, Universidade de São Paulo (USP) , São Paulo , Brazil .
Drug Dev Ind Pharm. 2015 Mar;41(3):430-5. doi: 10.3109/03639045.2013.877481. Epub 2014 Jan 13.
The performance of the standardized extrusion-spheronization technique, operational conditions, formulation parameters and storage of the final product over the bioactivity of papain containing pellets has been evaluated to obtain an insight into the potential of the technique for the manufacture of solid protein formulations. The pellets produced were assayed in terms of biological activity - monitored at each operational stage using N-benzoyl-dl-arginine ρ-nitroanilide as a substrate, and according to the physical properties - evaluated by means of size distribution, apparent density and friability. The produced pellets presented adequate physical and mechanical properties. Monitoring biological activity at each production stage revealed that the most critical steps corresponded to drying and storage, with bioactivity decay ranging from 5 to 30% and 5 to 20% for each process. Dry mixing and extrusion did not hold any influence over papain activity, while wet massing decreased the bioactivity by approximately 0-5% and the spheronization 0-2%. The results varied as a function of the experimental conditions and formulation components. In conclusion, the extrusion--spheronization technique was suitable to produce solid multiparticulate dosage forms for papain, considering the possibility to originate pellets with relatively low bioactivity decay. However, weak points of the technique corresponded to the wet massing and drying stages as well as storage.
已对标准化挤出滚圆技术的性能、操作条件、配方参数以及最终产品的储存对含木瓜蛋白酶微丸生物活性的影响进行了评估,以深入了解该技术在制备固体蛋白质制剂方面的潜力。所制备的微丸根据生物活性进行了测定——在每个操作阶段使用N-苯甲酰基-dl-精氨酸对硝基苯胺作为底物进行监测,并根据物理性质——通过粒度分布、表观密度和脆碎度进行评估。所制备的微丸呈现出足够的物理和机械性能。在每个生产阶段监测生物活性表明,最关键的步骤对应于干燥和储存,每个过程的生物活性衰减范围为5%至30%和5%至20%。干混和挤出对木瓜蛋白酶活性没有任何影响,而湿法制粒使生物活性降低约0-5%,滚圆使生物活性降低0-2%。结果因实验条件和配方成分而异。总之,考虑到有可能制备出生物活性衰减相对较低的微丸,挤出滚圆技术适合用于生产木瓜蛋白酶的固体多颗粒剂型。然而,该技术的弱点对应于湿法制粒、干燥阶段以及储存。