Ibrahim Y K, Olurinola P F
Hygiene-Institute, Universität Heidelberg.
Pharm Acta Helv. 1991;66(11):298-301.
Raw materials used for tablet production were assessed for their microbiological quality. Tablets were produced by wet granulation and direct compression methods and assessed for compliance with B.P. specifications. Samples from the production stages in the two tabletting processes were assessed for microbial levels and for absence from designated microbial species- E.coli, Ps.aeruginosa, S.aureus and salmonella species. The effect of the microbial levels of the raw materials and the formulation technology on the microbial levels of the produced tablets were also investigated. Results indicated that the microbial levels of the tablets were influenced by the microbial quality of the starting raw materials, the production environment and the method of production. Generally, tablets produced by direct compression method gave lower microbial levels than those of the wet granulation method. The compaction process exert lethal effect on the survival of microorganisms.
对用于片剂生产的原材料的微生物质量进行了评估。片剂通过湿法制粒和直接压片法生产,并评估其是否符合英国药典规范。对两种压片工艺生产阶段的样品进行微生物水平评估,并检测是否存在指定的微生物种类——大肠杆菌、铜绿假单胞菌、金黄色葡萄球菌和沙门氏菌属。还研究了原材料的微生物水平和制剂技术对所生产片剂微生物水平的影响。结果表明,片剂的微生物水平受起始原材料的微生物质量、生产环境和生产方法的影响。一般来说,直接压片法生产的片剂微生物水平低于湿法制粒法生产的片剂。压片过程对微生物的存活具有致死作用。