In this paper, The United States Pharmacopoeia ( USP) is introduced in terms of the history of publication, the constitution, the monograph and the future trend in the development.

1、

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

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。

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2、

Use HPLC to experiment the different test in USP Pharmacopeia and Europe Pharmacopeia, and contrast the relationship of these results. 3.

采用高效液相法分析美国药典、欧洲药典中对大蒜项下大蒜辣素的检查，对比结果的相近程度和关系。

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3、

Results The physicochemical properties of the laboratory product met the requirement of American Pharmacopoeia.

结果实验室产品理化性能符合美国《药典》同类产品要求。

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4、

The results showed good agreement with those obtained by cerium sulphate method.

本法与美国药典（ⅩⅪ版）硫酸铈法比较，结果一致。

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5、

The authors compared the validation requirements for alternative microbiological methods between USP1223 and Ph Eur5.1.6 in detail.

文章详细对比了美国药典1223和欧洲药典5.1.6对于微生物替代法验证要求的异同。

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6、

Don't adopt a USP that you can't deliver, or further marketing is useless.

不要采用美国药典您不能发表，或其它的市场营销是没有用处的。

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7、

The contents were in compliance with USP27/ NF22, which included identification, loss on drying, residue on ignition, heavy metals, free acid and content of acetyl.

内容基本依照美国药典（USP27／NF22）CA项，包括鉴别、干燥失重、炽灼残渣、重金属、游离酸、乙酰化率。

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8、

OBJECTIVE: To establish a method for the determination of taurine, and to compare which with that stated in Chinese Pharmacopoeia ( CP) and that stated in United States Pharmacopoeia ( USP).

目的：建立测定牛磺酸中主药及有关物质含量的方法，并与《中国药典》（药典）方法和《美国药典》（USP）方法比较。

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9、

Effect of Senna Extract on Gastrointestinal Motility and Histomorphology of Gastrointestinal Tract in Mice

番泻叶提取物对小鼠胃肠运动及其组织形态学的影响美国药典（24版）：番泻叶

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10、

Discussion about Determination of Paeoniflorin in Radix Paeoniae Alba in the Pharmacopeia of the People's Republic of China ( 2000 Ed) Volume I

美国药典（24版）：番泻叶对《中国药典》2000年版Ⅰ部白芍中芍药苷含量测定方法的探讨

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11、

Results show that various kinds of impurities in raw water can be removed by the system effectively and the product water satisfies all criteria for water for injection.

结果表明，该工艺设计合理，能有效去除原水中各种杂质，产品水符合中国药典及美国药典规定，是一种值得推广应用的新型药用水生产技术。

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12、

Methods The way of apparatus suitability test is described in the United States pharmacopoeia.

方法参照美国药典中溶出度仪的系统适用性校正方法。

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13、

Comparison of Content Uniformity Test between USP 29~ ( th) and ChP

美国药典29版与中国药典含量均匀度检查方法的比较分析

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14、

Study of the statistical characteristics of the USP ⅹⅺ content uniformity sampling plan for tablets

美国药典ⅩⅪ版片剂含量均匀度检验方案的统计特性分析

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15、

Comparing the Examination Methods of Vegetable Drugs in USP with that in Chp

美国药典植物药检查方法与中国药典相关项目的比较

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16、

Suitability test for apparatus of USP dissolution test Research on the Environmental Suitability Test

对美国药典溶出度装置适用性试验的考察

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17、

calcium perborate and magnesium peroxide are alkaline earth peroxide.

过硼酸钙与过氧化镁都是重要的碱土金属过氧化物。

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18、

effect of fluoride and fluoride plus calcium on serum lipid peroxide in ovariectomized rats

氟化物及氟化物加钙对卵巢切除大鼠血清中LPO变化的影响

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19、

tests carried out from 2001-2003 clarified that the factors needed for the cultivation method of rice direct sowing before flooding, such as suitable varieties, row spacing, density, sowing depth, and amount of calcium peroxide.

经过2001～2003年三年的试验研究，明确了寒地水稻折衷直播栽培的适宜品种、种植行距、密度、播深及供氧剂包衣对出苗的影响。

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20、

the transformation of phosphorus fractions in the sediments shows that diverse change of iron-bound phosphate are deemed to cause the effect under different adding options of calcium peroxide.

底泥磷的分级提取实验结果表明，铁磷的不同变化趋势是CaO2投加方式引起底泥磷释放不同效果的内在原因。

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