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作 者:张媛媛[1,2] 曹苋恺 李晓波 ZHANG Yuanyuan;CAO Xiankai;LI Xiaobo(Shanghai Jiao Tong University,Shanghai 200240,China;Shanghai Lvgushengmingyuan Pharmaceutical Co.,Ltd.,Shanghai 201707,China)
机构地区:[1]上海交通大学药学院,上海200240 [2]上海绿谷生命园医药有限公司,上海201707
出 处:《上海医药》2018年第13期80-83,共4页Shanghai Medical & Pharmaceutical Journal
摘 要:目的:建立中药抗菌药物紫苏方胶囊微生物限度检查方法并对其进行验证。方法:参照2015年版《中国药典》四部通则,利用卵磷脂、L组氨酸、聚山梨酯80的中和作用,采用薄膜过滤法和平皿法测定紫苏方胶囊对金黄色葡萄球菌等5种试验菌种的回收率,并对其进行了控制菌适用性试验。结果:5种试验菌回收率均在0.5~2.0范围,控制菌可检出。结论:本试验所建立方法可用于紫苏方胶囊的微生物限度检查。Objective: To establish and verify the microbial limit test method for the traditional Chinese medicine of Zisu Fang capsule. Methods: According to the fourth part of the 2015 edition of Chinese Pharmacopoeia principles, the recovery rates of Zisu Fang capsule against 5 kinds of test microorganisms including Staphylococcus aureus were measured by membrane filtration and Petri dish methods and using the neutralization of lecithin, L-histidine and polysorbate 80, and the applicability test of E.coli as the control bacterium was also performed. Results: The recovery rates of the 5 kinds of experimental microorganisms were in the range of 0.5-2, and the control bacterium could be detected. Conclusion: The methods established in this experiment can be used for the microbial limit test of Zisu Fang capsule.
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