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Pharm

The document contains a set of 30 multiple-choice questions (MCQs) related to bioavailability, drug metabolism, and pharmacology. Each question is followed by a list of answer options, with the correct answers provided at the end. The content covers various aspects of drug administration, absorption, metabolism, and the role of enzymes in these processes.

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0% found this document useful (0 votes)
22 views13 pages

Pharm

The document contains a set of 30 multiple-choice questions (MCQs) related to bioavailability, drug metabolism, and pharmacology. Each question is followed by a list of answer options, with the correct answers provided at the end. The content covers various aspects of drug administration, absorption, metabolism, and the role of enzymes in these processes.

Uploaded by

wmqs949g4w
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

BIOAVAILABILITY AND DISTRIBUTION – PRACTICE MCQs

​ 1.​ Which route of administration provides 100% bioavailability?

A) Oral

B) Intramuscular

C) Intravenous

D) Subcutaneous

​ 2.​ What primarily determines bioavailability?

A) Plasma protein binding

B) Absorption rate and absorption ratio

C) Molecular weight

D) Urinary excretion

​ 3.​ Which dosage form is absorbed the fastest?

A) Tablet

B) Capsule

C) Suspension

D) Solution

​ 4.​ Which of the following reduces drug bioavailability?

A) Enteric coating

B) Intravenous injection

C) P-glycoprotein in the intestine

D) Acid-stable drug

​ 5.​ What happens to a drug during first-pass metabolism?

A) It reaches the brain directly


B) It is excreted in urine

C) It is eliminated before entering systemic circulation

D) It bypasses the liver

​ 6.​ Which statement about absorption kinetics is true?

A) Zero-order drugs are absorbed faster with higher doses

B) First-order drugs are absorbed at a constant rate

C) First-order drug absorption increases with dose

D) Zero-order drugs have no Tmax

​ 7.​ Vancomycin has poor oral bioavailability because it is:

A) Lipophilic

B) Acid-stable

C) Very hydrophilic

D) A prodrug

​ 8.​ Which enzyme is mainly responsible for presystemic elimination?

A) Renin

B) Cytochrome P450

C) Lipase

D) Amylase

​ 9.​ Enterohepatic circulation prolongs drug action because:

A) Drugs are absorbed faster

B) Drugs are excreted faster

C) Drugs continuously cycle between liver and intestine

D) Drugs avoid metabolism

​ 10.​ Which parameter is most important in evaluating bioavailability?


A) Cmax

B) Tmax

C) Half-life

D) AUC

​ 11.​ If the AUC for oral drug is 50 and for IV is 100, the bioavailability is:

A) 100%

B) 50%

C) 10%

D) 200%

​ 12.​ A drug with zero-order kinetics will:

A) Be absorbed faster as dose increases

B) Be absorbed at a constant rate regardless of dose

C) Have variable half-life

D) Not show any plasma concentration

​ 13.​ Which drug is absorbed through passive diffusion better?

A) Ionized drug

B) Non-ionized drug

C) Hydrophilic drug

D) Charged molecule

​ 14.​ Lipophilic drugs require:

A) No carriers

B) Protein carriers

C) High solubility in water

D) Acidic pH
​ 15.​ Plasma protein that binds most drugs is:

A) Globulin

B) Lipoprotein

C) Albumin

D) Alpha-1-acid glycoprotein

​ 16.​ Which condition decreases albumin levels and increases free drug?

A) Dehydration

B) Hypoalbuminemia

C) Hyperkalemia

D) Hypernatremia

​ 17.​ Warfarin toxicity may occur when taken with aspirin because:

A) Aspirin inhibits its metabolism

B) Aspirin increases warfarin excretion

C) Aspirin displaces warfarin from plasma proteins

D) Aspirin slows gastric emptying

​ 18.​ Which drug has a narrow therapeutic index?

A) Paracetamol

B) Digoxin

C) Ibuprofen

D) Amoxicillin

​ 19.​ A lipophilic drug is likely to have:

A) Low protein binding

B) Low absorption

C) High protein binding


D) Poor membrane crossing

​ 20.​ Sequestration increases volume of distribution because:

A) Drug is cleared quickly

B) Drug accumulates in plasma

C) Drug accumulates in tissues

D) Drug is metabolized rapidly

​ 21.​ Thiopental’s action ends due to:

A) Metabolism

B) Excretion

C) Redistribution

D) Dilution

​ 22.​ A drug with a volume of distribution of 1000L is likely:

A) Highly bound to albumin

B) Mostly in plasma

C) Accumulated in tissues

D) Excreted via kidneys

​ 23.​ Which of the following can cause ion trapping?

A) Protein binding

B) Redistribution

C) pH difference

D) Liver failure

​ 24.​ Ion trapping increases drug excretion by:

A) Conjugation in liver

B) Making the drug non-ionized


C) Making the drug ionized in urine

D) Increasing lipophilicity

​ 25.​ Salicylate poisoning is treated by:

A) Acidifying the urine

B) Giving antibiotics

C) Alkalinizing the urine

D) Diuretics

​ 26.​ Highly lipophilic drugs:

A) Cannot cross membranes

B) Accumulate in adipose tissue

C) Are rapidly excreted in urine

D) Are poorly absorbed

​ 27.​ Drugs absorbed in their non-ionized form will:

A) Remain in GI tract

B) Be absorbed into plasma

C) Be trapped in kidneys

D) Be metabolized faster

​ 28.​ Which of the following is an efflux protein?

A) Cytochrome P450

B) Albumin

C) P-glycoprotein

D) Trypsin

​ 29.​ Drug redistribution occurs in this order:

A) Plasma → Kidney → Liver


B) Brain → Muscle → Fat

C) Intestine → Liver → Blood

D) Heart → Brain → Stomach

​ 30.​ Which drug binds to lipoproteins?

A) Digoxin

B) Quinine

C) Cyclosporine

D) Lidocaine

ANSWER KEY

​ 1.​ C

​ 2.​ B

​ 3.​ D

​ 4.​ C

​ 5.​ C

​ 6.​ C

​ 7.​ C

​ 8.​ B

​ 9.​ C

​ 10.​ D

​ 11.​ B

​ 12.​ B

​ 13.​ B

​ 14.​ B

​ 15.​ C
​ 16.​ B

​ 17.​ C

​ 18.​ B

​ 19.​ C

​ 20.​ C

​ 21.​ C

​ 22.​ C

​ 23.​ C

​ 24.​ C

​ 25.​ C

​ 26.​ B

​ 27.​ B

​ 28.​ C

​ 29.​ B

​ 30.​ C

Here are 30 MCQs based on the content of your pharmacology metabolism lecture. The
answers are provided at the end.

MCQs:

1.​ Where does drug metabolism primarily occur?​


A) Kidney​
B) Liver​
C) Lungs​
D) Intestine​

2.​ What is the primary purpose of metabolism in the liver?​


A) Making drugs lipophilic​
B) Making drugs nonpolar​
C) Converting drugs to inactive and polar forms​
D) Enhancing drug taste​

3.​ Which of the following is a prodrug?​


A) Morphine​
B) Enalapril​
C) Codeine​
D) Digoxin​

4.​ What is the metabolite of enalapril?​


A) Morphine​
B) Acrolein​
C) Enalaprilat​
D) Gabapentin​

5.​ Which enzyme converts codeine into morphine?​


A) CYP3A4​
B) CYP2C9​
C) CYP2D6​
D) MAO​

6.​ Which drug is excreted without being metabolized?​


A) Codeine​
B) Lithium​
C) Minoxidil​
D) Cyclophosphamide​

7.​ Phase I reactions include all EXCEPT:​


A) Oxidation​
B) Hydrolysis​
C) Conjugation​
D) Reduction​

8.​ Where are phase I enzymes primarily located?​


A) Cytoplasm​
B) Plasma​
C) Endoplasmic reticulum​
D) Nucleus​

9.​ Which reaction is exclusive to microsomal enzymes in Phase II?​


A) Sulfation​
B) Acetylation​
C) Glucuronidation​
D) Methylation​
10.​Which enzyme shows genetic polymorphism and is not inducible?​
A) CYP3A4​
B) CYP2C9​
C) CYP2D6​
D) CYP2E1​

11.​Which of the following undergoes acetylation and can cause lupus-like syndrome
in slow acetylators?​
A) Codeine​
B) Hydralazine​
C) Diazepam​
D) Digoxin​

12.​Which enzyme metabolizes nicotine?​


A) CYP1A2​
B) CYP2C9​
C) CYP2A6​
D) CYP2D6​

13.​Which reaction occurs in the cytoplasm in Phase II?​


A) Oxidation​
B) Glucuronidation​
C) Acetylation​
D) Hydrolysis​

14.​Which enzyme is responsible for metabolizing alcohol at high doses?​


A) MAO​
B) CYP2D6​
C) CYP2E1​
D) Aldehyde oxidase​

15.​What is a possible effect of CYP enzyme induction on prodrugs?​


A) Decreased activity​
B) Increased toxicity​
C) Increased therapeutic effect​
D) No change​

16.​Which enzyme metabolizes warfarin?​


A) CYP1A2​
B) CYP2C9​
C) CYP2D6​
D) CYP3A4​
17.​Which of the following undergoes spontaneous non-enzymatic breakdown?​
A) Diazepam​
B) Atracurium​
C) Acetaminophen​
D) Procaine​

18.​Which is the correct sequence for Isoniazid metabolism?​


A) Phase I then Phase II​
B) Only Phase I​
C) Only Phase II​
D) Phase II then Phase I​

19.​Which CYP enzyme is involved in metabolizing 50% of drugs?​


A) CYP2C19​
B) CYP3A4​
C) CYP2E1​
D) CYP1A2​

20.​Which drugs can cause prolonged apnea in those without plasma cholinesterase?​
A) Morphine​
B) Succinylcholine and mivacurium​
C) Diazepam and midazolam​
D) Cocaine and lidocaine​

21.​Which enzyme breaks down tamoxifen?​


A) CYP3A4​
B) CYP2C19​
C) CYP1A2​
D) CYP2E1​

22.​Which CYP enzyme is involved in the metabolism of caffeine?​


A) CYP1A2​
B) CYP2D6​
C) CYP2A6​
D) CYP3A4​

23.​Which of the following is not a phase I reaction?​


A) Reduction​
B) Hydrolysis​
C) Glucuronidation​
D) Oxidation​

24.​Which drug undergoes N-methylation?​


A) Acetaminophen​
B) Noradrenaline​
C) Morphine​
D) Digoxin​

25.​Which is true about CYP3A4?​


A) Responsible for metabolizing alcohol​
B) Metabolizes 50% of all drugs​
C) Genetically polymorphic​
D) Found in cytoplasm​

26.​What happens if CYP enzymes are inhibited?​


A) Drug clearance increases​
B) Drug effect decreases​
C) Drug accumulates, increasing side effects​
D) Drug becomes nonpolar​

27.​Which of the following induces CYP enzymes?​


A) Ketoconazole​
B) Fluconazole​
C) Rifampicin​
D) Cimetidine​

28.​Which drug inhibits CYP enzymes?​


A) Carbamazepine​
B) Phenytoin​
C) Griseofulvin​
D) Erythromycin​

29.​Which type of metabolite is more dangerous than its parent drug?​


A) Enalaprilat​
B) N-acetyl-p-benzoquinonimine​
C) Glucuronide​
D) Sulfate conjugate​

30.​Which enzyme metabolizes esters like procaine and succinylcholine?​


A) Acetylcholinesterase and pseudocholinesterase​
B) CYP3A4​
C) CYP2C9​
D) MAO​

Answers:
1.​ B
2.​ C
3.​ B
4.​ C
5.​ C
6.​ B
7.​ C
8.​ C
9.​ C
10.​C
11.​B
12.​C
13.​C
14.​C
15.​C
16.​B
17.​B
18.​D
19.​B
20.​B
21.​B
22.​A
23.​C
24.​B
25.​B
26.​C
27.​C
28.​D
29.​B
30.​A

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