目的：建立阿咖酚散的微生物限度检查法，并对该法进行方法学验证。
OBJECTIVE: To establish a microbial limit test method for Akafen powder and validate the methodology.
方法：采用2005年版《中国药典》(一部)附录“微生物限度检查法”项下相关内容进行方法学验证。
METHODS: the method verification was carried out in accordance with the microbial limit test recorded in the appendix of China Pharmacopeia (2005 edition, Volume I).
经方法学验证试验得出的检查方法可用于复方氨酚烷胺片剂、胶囊剂和颗粒剂的微生物限度检查。
The validation results showed that the method can be used for microbial limit test of compound paracetamol and amantadine hydrochloride tablets and capsules.
方法：以2株细菌、2株真菌对4种口服头孢拉定制剂做了微生物限度检查方法学的比较和验证实验。
Methods: the proposed method of the microbial limit tests of 4 kinds of oral cefradine was compared and verified by 2 strains of bacterium and 2 strains of fungus.
目的：对黄连上清丸微生物限度检查方法进行方法学验证。
Objective: To verify the microorganism limited inspecting method of Huanglian Shangqing pill.
经方法学验证试验得出的检查方法可用于驴胶补血颗粒、银杏叶胶囊的微生物限度检查。
The validation results showed that the method could be used for microbial limit test for Liujiaobuxue Granules and Yinxingye Capsules.
经方法学验证试验得出的检查方法可用于国玉伤痛宁软膏的微生物限度检查。
The validation results showed that the method could be used for microbial limit test for Guoyu Shangtongning Ointment.
目的：考察2005年版中国药典微生物限度检查方法学验证试验中加菌时间点的合理性。
Objective:To discussing the rationality for the time of adding the tested microorganisms with validate method in the microbial limit test which was described in the Chinese Pharmacopeia(ChP) 2005.
目的：对阿莫西林胶囊微生物限度检查方法进行方法学验证。
Objective: To verify the microorganism limited inspecting method of Amoxicillin Capsules.
现代细菌学研究的方法学始于19世纪晚期，包括建立细菌染色方法和在培养基中进行微生物分离的技术，当时的培养基是用明胶和琼脂固化的营养物质。
The modern methods of bacteriological technique began in the late 19th century with the use of stains and the development of methods of cultivating organisms on plates of nutrients.
目的对克拉霉素片微生物限度检查方法进行方法学验证。
Objective To verify the microbial limit test for clarithromycin tablet by methodology.
结论通过对该品种的方法学验证确定该制剂可采用常规法进行微生物限度检查，不需去除抑菌成分。
Conclusion The methodological validation determines that this preparation can be examined with conventional microbial limit test, no need to remove anti-bacterial components.
结论通过对该品种的方法学验证确定该制剂可采用常规法进行微生物限度检查，不需去除抑菌成分。
Conclusion The methodological validation determines that this preparation can be examined with conventional microbial limit test, no need to remove anti-bacterial components.
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