The problems of effective digits in the Chinese Pharmacopoeia are discussed.
讨论了《中国药典》中存在的有效数字问题。
Microbial limit tests were validated according to Chinese Pharmacopoeia Edition 2005.
按照《中国药典》2005版微生物限度检查方法进行验证试验。
Methods We testified and checked the microbial limit with 2005 "Chinese Pharmacopoeia".
方法按中国药典2005年版一部微生物限度检查法进行验证和试验。
Result the method can compatible with the validation test of Chinese Pharmacopoeia 2005 version.
结果本方法满足中国药典2005版验证试验的基本要求。
METHODS According to Chinese Pharmacopoeia(2000 edition), the rotating basket method was employed.
方法按中国药典所载转蓝法进行体外溶出度测定。
Methods the method was based on the membrane filtration of sterility test of Chinese Pharmacopoeia 2005.
方法按《中国药典》2005年版附录无菌检查法项下薄膜过滤法。
The test method was carried out according to the method in volume two, Chinese Pharmacopoeia Edition 2005.
本试验参照《中国药典》2005年版二部无菌检查法进行试验。
CONCLUSION: the dissolution of the optimized dispersed tablets is up to the standard of Chinese Pharmacopoeia.
结论：优化处方达到《中国药典》规定要求。
OBJECTIVE To establish a doable validation method for estimating the microbial limit tests in Chinese Pharmacopoeia.
目的建立一种可行的验证方法，对中国药典收载的微生物限度检查法的有效性进行评价。
OBJECTIVE: to study the preparation techniques of ibuprofen tablet to meet the standard of Chinese pharmacopoeia 1995.
目的：探讨制备布洛芬片新的工艺条件，以达到中国药典1995年版新标准。
CONCLUSION: the dispersible tablets prepared are in conformity with the standards specified in Chinese Pharmacopoeia (2005).
结论：该分散片符合《中国药典》2005年版的相关规定。
Results: Each index is accorded with the quality level re - quest in Chinese Pharmacopoeia 2005 in the 2 years validity time.
结果：二年实际有效期内各项指标符合中国药典2005版质量标准要求。
Methods the 5 control strains recovery test validation method was used as described in the Chinese Pharmacopoeia 2005 edition.
方法按中国药典2005版有关规定，采用5种阳性对照菌回收率试验进行其方法学验证试验。
Results the colony recovery of membrane filtration method meets the related regulations of Chinese Pharmacopoeia (2005 edition).
结果：薄膜过滤法的菌落回收率符合2005年版《中国药典(二部)》相关规定。
In addition, the author questioned and discussed possible problems existed in the relative instruction of《Chinese Pharmacopoeia》.
同时也推断论证了《中国药典》中有关红景天药材来源的说明中出现的问题。
Objective:To develop a method of TLC to fecorded Rhizoma Alismatis in variety of Diwuang pills included in Chinese Pharmacopoeia.
目的：建立中国药典收载的地黄丸系列品种中泽泻的TLC鉴别方法。
Methods: the test was performed by the Turbidimetric-kinetic method that had been given by the Chinese Pharmacopoeia (Edition 2000).
方法：采用《中国药典2000年版》二部附录中检测细菌内毒素的动态浊度法。
Objective to replace the developing agents benzene and toluene in thin-layer chromatography in the Chinese Pharmacopoeia 2005 Volume I.
目的替换《中国药典》(2005年版一部)薄层鉴别中使用苯和甲苯的展开剂。
Methods: 13 different batches of cefradine capsules manufactured by 5 factories, were evaluated according to the Chinese Pharmacopoeia.
方法：按药典方法对5厂家效期内13批次的头孢拉定胶囊剂进行检测。
Conclusion: the garlic emulsion prepared by this composition and technology accords with the stipulation of Chinese Pharmacopoeia (2005).
结论：用该工艺制备的大蒜乳剂符合《中国药典》2005年版乳剂要求。
CONCLUSIONS the dispersible tablets accord with the requirement of the Chinese Pharmacopoeia (2000). The method of quality control is reliable.
结论：该分散片符合中国药典2 0 0 0年版的规定，质量控制方法可靠。
OBJECTIVE: To discuss the classification of Bulbus Fritillariae Cirrhosae medical materials indexed in different versions of Chinese Pharmacopoeia.
目的：探讨历版《中国药典》所载川贝药材的商品分类。
METHODS The dissolution of nimodipine in vitro was tested according to Chinese pharmacopoeia 2000, using the first method with RC dissolution tester.
方法按中国药典2000年版附录中转篮法测定尼莫地平片在人工胃液中的溶出度；
METHODS:Heavy metals in the purified water were detected by the refined testing water specifically for detection in accordance with Chinese Pharmacopoeia .
方法：采用精制处理后的检查专用试验水，按《中国药典》方法检查纯化水中的重金属。
The apparatus proves stable by long-time operational testing. The product water accords with the criterion of purified water in the Chinese Pharmacopoeia 2000.
经长时间运行考核，该装置性能稳定，产水水质符合中国药典2000年版“纯化水”标准。
Therefore, in our experimental courses of Titrimetric Analysis, the important tool of pharmaceutists, Chinese Pharmacopoeia, is used into the designed experiments.
在分析化学实验课中设置与《中国药典》相结合的容量分析法设计性实验，可获得较好的教学效果。
The bacterial endotoxin testing method for Huangqi Injection was set up, by the bacterial endotoxin test was approved according to Chinese Pharmacopoeia 2005 edition.
建立黄芪注射液的细菌内毒素检查法。依据《中国药典》2005年版附录细菌内毒素检查法进行试验。
CONCLUSION the compound was reported in domestic literature for the first time, providing reference for the improvement of oxazepam standard of Chinese pharmacopoeia.
结论该化合物为奥沙西泮的降解产物，在国内首次报道，为《中国药典》中奥沙西泮的质量标准提高提供了科学依据。
Objective To evaluate uncertainty for concentration of hydrochloric acid standard solution prepared and standardized with the method in Chinese Pharmacopoeia (edition 2005).
目的对按照2005年版《中国药典》方法配制和标定的盐酸标准溶液浓度进行不确定度评定。
Objective To evaluate uncertainty for concentration of hydrochloric acid standard solution prepared and standardized with the method in Chinese Pharmacopoeia (edition 2005).
目的对按照2005年版《中国药典》方法配制和标定的盐酸标准溶液浓度进行不确定度评定。
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