药典

并按药典规定测定溶液pH值，比较pH值与其发生沉淀的关系。

The pH Values of related solution were tested according to the request of pharmacopeia . By comparison , the relation between pH value of the solution and precipitate was established .

所含的Rg1和Rb1的总量均符合《中国药典》2000年版中三七的质量要求。

The contents of ginsenoside Rg_1 and Rb_1 were in accordance with China Pharmacopeia of year 2000 edition .

中国的《唐本草》是世界上最早的一部国家药典。编成于唐朝唐高宗显庆4年（公元659年）。

“ The Tang Ben Cao ”, completed in the fourth year of the reign of Emperor Gaozong ( Xian Qing ) of the Tang Dynasty ( 618 A.D. - 907 A.D. ), was the earliest book on medicine in the world .

维生素C注射液药典方法的补充与建议①.有关物质的检测和规定。

Vitamin C Injection Pharmacopoeia method supplemented with ① For substances testing and regulations .

目的比较2000年版药典收载黄芪品种及其民间习用品的DNA指纹图谱和有效成分黄芪甲苷、总黄酮及总多糖的含量，对黄芪质量标准进行多维研究。

OBJECTIVE To compare DNA fingerprinting and active compound contents among different species of Radix Astragali .

各国药典中关于庆大霉素C组分的测定方法均为高效液相色谱法，但检测方式及分离效果不同。

The results were compared for determining gentamycin C components by high performance liquid chromatography with different detectors in pharmacopoeias .

方法：采用中国药典2005年版无菌检查法中的薄膜过滤法（附录ⅪH）。

Method : Verification test in Pharmacopeia of P. R. China ( Chp ) 2005 was used .

方法：HPLC测定黄酮类成分橙皮苷和柚皮苷含量、生物碱类辛弗林含量，药典法测定挥发油含量。

Method : HPLC analysis was performed to detect the contents of hesperidin , naringin and synephrine .

另外，参考《中华人民共和国药典》（2005版）和《英国药典》（2003），对氯硝柳胺分析方法进行了改进，制订了HPLC分析方法。

With referrence of Chinese pharmacopoeia and British pharmacopoeia , the HPLC analysis method of niclosamide has been made .

与用普通溶剂结晶相比，发现采用超临界CO2结晶所得葛根素的溶剂残留最少、与中国药典中的标准红外光谱最为接近、品质更优。

Compared with normal solvents , crystal from super critical fluid extraction had the fewest residue solvents ; best quality and shape ;

从细胞色素P（450）酶角度归纳2005年版《中国药典》收载的中成药与其它药物不合理配伍使用情况

On the Compatibility of Chinese Traditional Patent Medicine Indexed in China Pharmacopoeia ( 2005 Edition ) in Combination with Other Drugs from the Perspective of Cytochrome P_ ( 450 ) Enzyme

方法：TLC法按中国药典2000年版格列吡嗪片有关物质检查薄层色谱条件；

Methods : The TLC was concordant with the method described in Chinese Pharmacopoeia 2000 ;

方法现版中国药典与美国药典均采用TLC法。

METHOD TLC Methods has been adopted in current edition of CP as well as in USP .

本文通过6个独立周期实验，考察了中国药典1995年版庆大霉素C组分测定方法的重复性。

A primary research on the determination of component C in Gentamycin Sulphate has been made through a six-period independent experiment to study the repeatability of Chinese Pharmacopoeia ( 95th ) method .

对于茶苯海明口崩片，则以日本药典（JP）溶出度改良法较为适合。

Improved-JP dissolution disintegrating method was optimum for the measurement dimenhydrinate ODT .

F检验结果表明该方法精密度与药典方法相当；

RESULTS The precision of Highly-accurate nephelometric titration was better than 0.2 % under suitable experiment conditions , which was comparable to that of the Pharmacopoeia methods by F-test .

方法体外释放采用中国药典2000年版二部的转篮法，体内血药浓度以RP-HPLC法测定，以DAS软件计算药动学参数。

Methods Determine the in vitro dissolution by rotating basket method and the in vivo serum concentrations by RP-HPLC .

经HPLC分析得产品纯度为98.1%，顺反比例为9.1/91.9，符合药典的要求。

The purity of product analyzed by HPLC was 98.1 % and ratio of cis-form and trans-form was 9.1 / 91.9 , which conformed to the criterion of pharmacopoeia .

方法采用现版的不同药典的相关HPLC法及HPLC-MS分析，研究头孢噻肟钠的完全杂质谱。

Methods The current HPLC methods in different pharmacopoeia and HPLC-MS analysis were performed to study on the complete impurity profile of Cefotaxime Sodium .

实验了pH值、有机溶剂、放置时间和干扰离子对测定的影响，该法简便快速，可用于相关药品检验，与药典方法对照，结果吻合。

Effects of pH , organic solvents and foreign ions on the determination of both drugs were examined . This method was rapid and simple and can be used for determining carvedilol and ampicillin sodium .

方法：结合红霉素效价测定实例，依据《中国药典》2000年版二部附录的要求，利用Excel表格的各种函数、公式编辑等功能，进行编程与优化。

Methods : Based on Chinese pharmacopoeia 2000 , using a sample of erythromycin 's potency assay , the program was established and optimized with some Excel functions and formulas .

检查：粒度15%、水分含量6%、溶化性、装量差异均符合《中国药典》2010年版一部附录Ⅰ制剂通则ⅠC颗粒剂项下的相关规定。

Inspect : particle size 15 % , and moisture content 6 % . Dissolubility and differences among packs were consistent with the preparation principals for IC granules in the appendix I of the primary part of the Chinese pharmacopeia 2010 .

道地产区和GAP基地药材挥发油含量和桂皮醛含量均符合药典规定，商品药材含油量和含醛量波动大。

Cinnamyl aldehyde contents and volatile oil yields for samples from genuine producing areas and GAP planting base were up to the pharmacopoeia . There was a great fluctuation in cinnamyl aldehyde contents and volatile oil yields in commercial materials .

测试溶液（TS）的信息已在美国药典的试剂，指示物和溶液章节测试溶液部分中被提供。

Information on Test Solutions ( TS ) is provided in the Test Solutions portion of the Reagents , Indicators , and Solutions section of the USP – NF .

筛选出最佳基质为甘油明胶，与利福平的最佳配比为5∶1，其融变时限为（25.6±0.94）min，符合中国药典要求。

The best base was glycerin-glutin , its best proportion to RFP was 5 ∶ 1 , and its melt time was ( 25.6 ± 0.94 ) min , according to the request of Chinese pharmacopoea .

方法参照美国药典（USP）23版木瓜酶活力的测定方法，采用正交试验法对国内外测定条件进行了逐项试验的研究，筛选出最佳测定条件。

METHOD Base on determination of enzymatic active for papain in USP ⅹⅹⅲ . The analytical conditions were selected by orthogonal tests .

该章讨论的是USP纯化水和非药典规定的水的制备过程相关的基本系统结构和终处理工艺。

This chapter discusses the final treatment technologies and basic system configurations related to the manufacturing process of USP Purified Water and non-compendial water .

方法：按《中国药典》（二部）2000年版规定，用不同厂家生产的鲎试剂（TAL）对SAGM红细胞保存液进行细菌内毒素检查法干扰试验。

METHODS : Interference test was carried on endotoxin detection of SAGM erythrocyte preserve fluid with test agent of limulus ( TAL ) .

方法：MUG-Indole法和中国药典法配对试验。

METHOD : MUG-Indole method and cp method were performed by conjugation test .

可根据NDA文件中描述的更为详尽的概念来制订限度，包括药典正文适当性的检查。

Limits can then be set based on the more detailed concepts described for NDA filing , including review of compendial monographs for appropriateness .