2021 Pharmaceutical Analysis(中国药科大学) 最新满分章节测试答案

文章目录[隐藏]

1.Drug Quality Standard and Quality Control Quizzes：Drug Quality Standard and Quality Control
2.Pharmaceutical Analysis Methodology Quizzes：Pharmaceutical Analysis Methodology
3.Bioanalytical Method Quizzes：Bioanalytical Method
4.Analytical Methods for Biological Products Quizzes：Analytical Methods for Biological Products
5.Analytical Methods for Traditional Chinese Medicine Quizzes：Analytical Methods for Traditional Chi
【作业】6.Genetic Polymorphism Detection Techniques Task：Genetic Polymorphism Detection Techniques
7.Quality Control of Chemical Drugs and Antibiotics Quizzes：Quality Control of Chemical Drugs and An
8. Drug Clinical Trial Monitoring Quizzes： Drug Clinical Trial Monitoring

本答案对应课程为:点我自动跳转查看
本课程起止时间为:2021-01-04到2021-03-01
本篇答案更新状态:已完结

1.Drug Quality Standard and Quality Control Quizzes：Drug Quality Standard and Quality Control

1、问题:The principle of English names for drugs in Chinese Pharmacopoeia follows（） formulated by the World Health Organization.
选项：
A:ChP
B:CADN
C:INN
D:BNF
答案: 【INN】

2、问题:The content of pharmaceutical preparations is expressed as （）.
选项：
A:Weight percentage
B:Molar percentage content
C:Volume percentage
D:Labeled amount percentage content
答案: 【Labeled amount percentage content】

3、问题:According to the provisions of drug quality standards, evaluating the quality of a drug uses （）.
选项：
A:Identification, inspection, quality determination
B:Bioavailability
C:Physical properties
D:Pharmacological effects
答案: 【Identification, inspection, quality determination】

4、问题:The full name for ICH is （）
选项：
A:Import drug registration standards
B:European Pharmacopoeia
C:United States Pharmacopoeia-National Formulary
D:International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use
答案: 【International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use】

5、问题:In Chinese Pharmacopoeia, the general analysis and determination methods are contained in（）
选项：
A:Volume I
B:Volume II
C:Volume III
D:Volume IV
E:Supplement
答案: 【Volume IV】

6、问题:Regarding the Chinese Pharmacopoeia, the most appropriate statement is （）
选项：
A:A book about drug analysis
B:A book containing all medicines produced in China
C:National legal technical standards for supervision and management of drug quality
D:A dictionary about drugs
E:Technical specifications on Chinese herbal medicines and Chinese patent medicines
答案: 【National legal technical standards for supervision and management of drug quality】

7、问题:There are a total of 36 pieces raw materials entering a factory, and the number of random samples should be （）
选项：
A:5 pieces
B:6 pieces
C:7 pieces
D:36 pieces
答案: 【7 pieces】

8、问题:The basic sequence of drug inspection work is （）
选项：
A:retain samples → inspection → sampling → report
B:inspection → sampling → retaining sample → report
C:sampling → inspection → report → sample retention
D:sampling → inspection → sample retention → report
答案: 【sampling → inspection → sample retention → report】

9、问题:"Precision weighing" in “Chinese Pharmacopoeia” means that the weight should be accurate to （） of the weight taken.
选项：
A:± 10%
B:1%
C:1‰
D:1‱
E:millionth
答案: 【1‰】

10、问题:"Easily soluble" means that 1g (ml) of solute can be dissolved in ( ) solvent.
选项：
A:Less than 1ml
B:1ml～10ml
C:10ml～30ml
D:100ml～1000ml
E:1000 ml～10000ml
答案: 【1ml～10ml】

11、问题:The cool and dark place of the drug storage conditions means （）
选项：
A:No more than 20 ℃
B:Avoid light, not exceeding 20 ℃
C:2 ℃ ～ 10 ℃
D:Avoid light, 10 ℃ ～ 30 ℃
E:Avoid light, 10 ℃ ～ 25 ℃
答案: 【Avoid light, not exceeding 20 ℃】

12、问题:The requirements for drug inspection sampling are （）
选项：
A:Scientificalness
B:Authenticity
C:representativeness
D:rigorism
答案: 【Authenticity;
representativeness】

13、问题:The drug quality standard is （）
选项：
A:Technical regulations on drug quality specifications and inspection methods
B:Legal basis followed by departments engaged in pharmaceutical production and inspection
C:The legal basis followed by the drug supply and use departments
D:Legal basis followed by drug supervision and administration departments at all levels
E:Contents that must be included in the drug instructions
答案: 【Technical regulations on drug quality specifications and inspection methods;
Legal basis followed by departments engaged in pharmaceutical production and inspection;
The legal basis followed by the drug supply and use departments;
Legal basis followed by drug supervision and administration departments at all levels】

14、问题:In the following methods, ( ) can be used to identify drugs.
选项：
A:Chemical methods
B:Spectrophotometry
C:Chromatography
D:Biological methods
E:Nonaqueous titration
答案: 【Chemical methods;
Spectrophotometry;
Chromatography;
Biological methods】

15、问题:The content contained in Volume IV of the Chinese Pharmacopoeia 2015 edition includes（）
选项：
A:Chinese herbal medicines and prescriptions
B:Standards for chemical medicines
C:General notices and general chapters
D:Standards for biological products
E:Standards for medicinal excipients
答案: 【General notices and general chapters;
Standards for medicinal excipients】

2.Pharmaceutical Analysis Methodology Quizzes：Pharmaceutical Analysis Methodology

1、问题:Using chemical analysis and instrumental analysis to determine drug content is referred to as ( ) in drug quality standards.
选项：
A:potency determination
B:biological standardization
C:content determination
D:drug control
答案: 【content determination】

2、问题:The determination of drug content by biological or enzymatic chemical methods is called ( ).
选项：
A:potency determination
B:bbiological standardization
C:content determination
D:drug control
答案: 【potency determination】

3、问题:Titrate is ( ) for each 1 ml of titrant at the specified concentration.
选项：
A:the mole number of the drug measured
B:the mass of the drug measured
C:the mole number of the standard substance
D:the mass of the standard substance
答案: 【the mass of the drug measured】

4、问题:In the following statements of volumetric analysis used for content determination, the incorrect one is ( ).
选项：
A:simple operation
B:accurate results
C:good durability
D:high specificity
答案: 【high specificity】

5、问题:According to pharmacopoeia, the precisely calibrated titrant (such as hydrochloric acid and its concentration) is correctly expressed as ( )
选项：
A:Hydrochloric acid titrant（0.1520M）
B:Hydrochloric acid titrant（0.1520mol/L）
C:Hydrochloric acid titrant（0.1520M/L）
D:0.1520M Hydrochloric acid titrant
答案: 【Hydrochloric acid titrant（0.1520mol/L）】

6、问题:In volumetric analysis, the burette reading can be estimated to be ±0.02ml. In order to ensure the error of analysis results not exceed 0.1%, the volume of titrant should be ( ).
选项：
A:10ml
B:15~20ml