大学MOOC PharmaceuticalAnalysis(中国药科大学)1462646217 最新慕课完整章节测试答案
1.DrugQualityStandardandQualityControl
文章目录
QuizzesDrugQualityStandardandQualityControl
1、单选题：
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、单选题：
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、单选题：
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、单选题：
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、单选题：
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、单选题：
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、单选题：
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、单选题：
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、单选题：
"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、单选题：
"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、单选题：
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、多选题：
The requirements for drug inspection sampling are （ ）
选项：
A: Scientificalness
B: Authenticity
C: representativeness
D: rigorism
答案: 【 Authenticity;
representativeness】
13、多选题：
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、多选题：
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、多选题：
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.PharmaceuticalAnalysisMethodology
QuizzesPharmaceuticalAnalysisMethodology
1、单选题：
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、单选题：
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、单选题：
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、单选题：
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、单选题：
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、单选题：
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
C: about 15ml
D: >20ml
答案: 【 >20ml】
7、单选题：
In reverse phase chromatography, the order of peak with large polarity substances and small polarity substances is ( ).
选项：
A: the one with high polarity goes out first
B: the one with small polarity goes out first
C: they go out at the same time
D: the order is different according to the situation
答案: 【 the one with high polarity goes out first】
8、单选题：
Unless otherwise specified, the trailing factor shall be ( ).
选项：
A: between 0.5 and 1.5
B: greater than 1.5
C: between 0.95 and 1.05
D: less than 2.0
答案: 【 between 0.95 and 1.05】
9、单选题：
The degree to which the measured results are close to the true or reference values is called ( ).
选项：
A: precision
B: accuracy
C: limits of detection
D: specificity
答案: 【 accuracy】
10、多选题：
( ) are often used as indicators in non-aqueous acid method.
选项：
A: Azoviolet
B: Crystal violet
C: Thymol blue
D: Bromophenol blue
答案: 【 Azoviolet;
Thymol blue;
Bromophenol blue】
11、多选题：
When titrating aspirin, neutral ethanol is used as solvent because ( ).
选项：
A: non-aqueous titration does not permit the use of water
B: it can prevent hydrolysis of the ester bonds during titration
C: commercial ethanol which can be used after the neutralization of sodium hydroxide shows weak acidity in phenolphthalein
D: aspirin is more soluble in ethanol
答案: 【 it can prevent hydrolysis of the ester bonds during titration;
commercial ethanol which can be used after the neutralization of sodium hydroxide shows weak acidity in phenolphthalein】
12、多选题：
Acid base titration commonly used titrant solutions include ( ).
选项：
A: sodium chloride
B: sodium hydroxide
C: hydrochloride aicd