摘要
目的:探讨不同企业生产的培养基用于2015年版《中国药典》沙门菌检查的可行性。方法:采用理化属性、适用性检查、生化试验、活菌检出四个方面对五个生产企业生产的培养基与实验室配制的培养基进行比对试验。结果:五个生产企业的相关培养基质量符合2015年版《中国药典》沙门菌检查的要求,实验室自行配制的RV和XLD等培养基因受诸多因素的影响不够理想。结论:研究结果可用于沙门菌检查用培养基质量控制依据。
Objective To discuss the feasibility of culture mediums produced by different enterprises for salmonella examination in Chi nese Pharmacopoeia 2015 Edition. Methods： Comparative study on physical and chemical properties, applicability inspection, bio chemical tests and sample tests were carried out. Results： The quality of culture mediums produced by five enterprises conformed to the requirements of salmonella examination in Chinese Pharmacopoeia 2015 Edition. The samples prepared in the laboratory such as RV, XLD were not good enough because of the influence of many factors. Conclusion： The comparison results can be used as quality basis of culture mediums for salmonella examination.
出处
《中国药品标准》
CAS
2014年第1期19-23,共5页
Drug Standards of China
关键词
沙门菌检查
培养基
质量研究
salmonella examination
culture mediums
quality research
