MCQ Quiz: Oral Drug Delivery

Oral drug delivery is the most widely used route of drug administration due to its convenience, non-invasiveness, and high patient compliance. It encompasses a variety of dosage forms such as tablets, capsules, liquids, and powders. This quiz will help Pharm.D. students strengthen their understanding of formulation principles, pharmacokinetics, drug release mechanisms, and barriers affecting oral bioavailability.

1. Which of the following is a primary advantage of oral drug delivery?

  • A. Avoids systemic absorption
  • B. Suitable for unconscious patients
  • C. Convenient and widely accepted by patients
  • D. Requires sterile formulation
    Correct answer: C. Convenient and widely accepted by patients

2. The first-pass effect refers to:

  • A. Drug absorption in the lungs
  • B. Drug metabolism in the liver before systemic circulation
  • C. Immediate therapeutic effect
  • D. Passage through the blood-brain barrier
    Correct answer: B. Drug metabolism in the liver before systemic circulation

3. Which dosage form is designed to release drug slowly over time?

  • A. Immediate-release tablet
  • B. Extended-release capsule
  • C. Sublingual tablet
  • D. Oral suspension
    Correct answer: B. Extended-release capsule

4. A disintegrant in a tablet serves to:

  • A. Prolong drug action
  • B. Increase tablet hardness
  • C. Facilitate breakdown of the tablet in the digestive tract
  • D. Act as a preservative
    Correct answer: C. Facilitate breakdown of the tablet in the digestive tract

5. What is the typical site of drug absorption for most orally administered drugs?

  • A. Stomach
  • B. Mouth
  • C. Small intestine
  • D. Colon
    Correct answer: C. Small intestine

6. Which factor most significantly affects oral drug bioavailability?

  • A. Drug color
  • B. Packaging material
  • C. First-pass metabolism
  • D. Tablet shape
    Correct answer: C. First-pass metabolism

7. What is a major disadvantage of oral drug delivery?

  • A. Requires intravenous access
  • B. Risk of systemic infection
  • C. Slower onset of action compared to parenteral routes
  • D. Always bypasses liver metabolism
    Correct answer: C. Slower onset of action compared to parenteral routes

8. Enteric-coated tablets are designed to:

  • A. Dissolve in the stomach
  • B. Increase flavor
  • C. Resist stomach acid and dissolve in the intestine
  • D. Act as chewables
    Correct answer: C. Resist stomach acid and dissolve in the intestine

9. Which of the following is a solid oral dosage form?

  • A. Emulsion
  • B. Capsule
  • C. Elixir
  • D. Suspension
    Correct answer: B. Capsule

10. Sublingual tablets are used to:

  • A. Delay onset
  • B. Provide local effect only
  • C. Bypass the first-pass effect for rapid absorption
  • D. Promote digestion
    Correct answer: C. Bypass the first-pass effect for rapid absorption

11. A liquid oral formulation that requires shaking is likely a:

  • A. Syrup
  • B. Suspension
  • C. Solution
  • D. Emulsion
    Correct answer: B. Suspension

12. Which excipient enhances palatability in pediatric oral drugs?

  • A. Binder
  • B. Disintegrant
  • C. Sweetener
  • D. Lubricant
    Correct answer: C. Sweetener

13. Buccal drug delivery refers to:

  • A. Absorption via the colon
  • B. Absorption through the stomach wall
  • C. Absorption through the cheek mucosa
  • D. Topical application
    Correct answer: C. Absorption through the cheek mucosa

14. Which formulation is best for patients with swallowing difficulties?

  • A. Extended-release tablet
  • B. Enteric-coated tablet
  • C. Oral liquid (e.g., solution or suspension)
  • D. Subcutaneous injection
    Correct answer: C. Oral liquid (e.g., solution or suspension)

15. The function of a lubricant in tablet formulation is to:

  • A. Improve taste
  • B. Reduce tablet hardness
  • C. Prevent sticking during manufacturing
  • D. Color the drug
    Correct answer: C. Prevent sticking during manufacturing

16. Orally disintegrating tablets (ODTs) are beneficial because they:

  • A. Are injectable
  • B. Require chewing
  • C. Dissolve quickly in the mouth without water
  • D. Must be swallowed whole
    Correct answer: C. Dissolve quickly in the mouth without water

17. Drugs that undergo significant hepatic metabolism are poorly suited for:

  • A. Buccal delivery
  • B. Sublingual delivery
  • C. Oral delivery
  • D. Inhalation
    Correct answer: C. Oral delivery

18. Which formulation is considered a monophasic oral liquid?

  • A. Suspension
  • B. Emulsion
  • C. Solution
  • D. Granules
    Correct answer: C. Solution

19. The rate of disintegration of a tablet directly influences:

  • A. Drug color
  • B. Drug absorption
  • C. Syrup viscosity
  • D. Flavor intensity
    Correct answer: B. Drug absorption

20. Which factor can increase oral drug absorption?

  • A. Poor solubility
  • B. High first-pass metabolism
  • C. High lipophilicity and membrane permeability
  • D. Complexation with ions
    Correct answer: C. High lipophilicity and membrane permeability

21. Which route bypasses hepatic first-pass metabolism?

  • A. Oral tablets
  • B. Sublingual
  • C. Enteric-coated tablets
  • D. Oral suspensions
    Correct answer: B. Sublingual

22. Which condition may reduce oral drug absorption?

  • A. Normal gastric emptying
  • B. Delayed gastric emptying
  • C. Fasting state
  • D. High water intake
    Correct answer: B. Delayed gastric emptying

23. Why are some oral tablets scored?

  • A. For decoration
  • B. To split doses easily
  • C. To increase hardness
  • D. To prevent swallowing
    Correct answer: B. To split doses easily

24. An oral drug with poor aqueous solubility may benefit from:

  • A. Enteric coating
  • B. Co-administration with food
  • C. Nanoparticle formulation or solid dispersion
  • D. Rapid elimination
    Correct answer: C. Nanoparticle formulation or solid dispersion

25. The bioavailability of an oral drug is defined as:

  • A. The time taken to reach peak plasma level
  • B. The rate and extent of drug reaching systemic circulation
  • C. The taste of the formulation
  • D. The binding to plasma proteins
    Correct answer: B. The rate and extent of drug reaching systemic circulation

26. Which formulation would have the fastest onset of action?

  • A. Enteric-coated tablet
  • B. Extended-release tablet
  • C. Oral solution
  • D. Controlled-release capsule
    Correct answer: C. Oral solution

27. A poorly compressible powder is best formulated as a:

  • A. Solution
  • B. Capsule
  • C. Hard tablet
  • D. Rectal suppository
    Correct answer: B. Capsule

28. A drug with high acid sensitivity should be formulated as a:

  • A. Syrup
  • B. Buccal lozenge
  • C. Enteric-coated tablet
  • D. Chewable tablet
    Correct answer: C. Enteric-coated tablet

29. Which of the following can enhance the dissolution rate of a poorly soluble drug?

  • A. Increasing particle size
  • B. Using wax coatings
  • C. Micronization
  • D. Decreasing porosity
    Correct answer: C. Micronization

30. Buccal administration avoids:

  • A. Rapid absorption
  • B. Patient cooperation
  • C. First-pass metabolism
  • D. Local effect
    Correct answer: C. First-pass metabolism

31. Which form offers both systemic and local effects in the GI tract?

  • A. Sublingual tablet
  • B. Enteric-coated capsule
  • C. Oral solution
  • D. Chewable antacid
    Correct answer: D. Chewable antacid

32. Which of the following is true about hard gelatin capsules?

  • A. Cannot be filled with liquids
  • B. Are chewable
  • C. Are made of two parts that can be filled with powder
  • D. Dissolve only in acid
    Correct answer: C. Are made of two parts that can be filled with powder

33. Oral syrups contain:

  • A. Emulsified oils
  • B. Alcohol only
  • C. A concentrated aqueous sugar solution
  • D. Micelles
    Correct answer: C. A concentrated aqueous sugar solution

34. Which is a risk with crushed extended-release tablets?

  • A. Enhanced palatability
  • B. Dose dumping and toxicity
  • C. Slower action
  • D. Reduced dissolution
    Correct answer: B. Dose dumping and toxicity

35. What determines the choice between tablet and capsule form?

  • A. Drug name
  • B. Cost alone
  • C. Drug stability, release profile, and patient preference
  • D. Pharmacist opinion
    Correct answer: C. Drug stability, release profile, and patient preference

36. The site of absorption for enteric-coated drugs is:

  • A. Buccal mucosa
  • B. Colon
  • C. Stomach
  • D. Small intestine
    Correct answer: D. Small intestine

37. A drug given orally in enteric-coated form should NOT be:

  • A. Given before meals
  • B. Taken with milk
  • C. Crushed
  • D. Given with water
    Correct answer: C. Crushed

38. Oral suspensions must be:

  • A. Clear
  • B. Stored in the freezer
  • C. Shaken before use
  • D. Given IV
    Correct answer: C. Shaken before use

39. A powder that absorbs moisture from the air is called:

  • A. Hygroscopic
  • B. Isotonic
  • C. Volatile
  • D. Neutral
    Correct answer: A. Hygroscopic

40. A liquid oral drug with two immiscible phases is a:

  • A. Suspension
  • B. Solution
  • C. Emulsion
  • D. Decoction
    Correct answer: C. Emulsion

41. Patient education for oral meds should include:

  • A. Color of the tablet
  • B. Brand name only
  • C. Administration instructions and storage tips
  • D. Pharmacokinetics lecture
    Correct answer: C. Administration instructions and storage tips

42. An advantage of chewable tablets is:

  • A. Slow onset
  • B. Bypassing taste receptors
  • C. Improved compliance in pediatrics
  • D. Enteric protection
    Correct answer: C. Improved compliance in pediatrics

43. Which form is best for water-insoluble drugs?

  • A. Aqueous solution
  • B. Syrup
  • C. Emulsion or suspension
  • D. Sublingual tablet
    Correct answer: C. Emulsion or suspension

44. What limits use of oral drug delivery in emergencies?

  • A. Excessive absorption
  • B. Long expiration
  • C. Slower onset of action
  • D. Incomplete metabolism
    Correct answer: C. Slower onset of action

45. Which form provides the fastest onset in oral administration?

  • A. Chewable tablet
  • B. Oral solution
  • C. Enteric-coated tablet
  • D. Extended-release capsule
    Correct answer: B. Oral solution

46. Sublingual nitroglycerin is used for:

  • A. Flu treatment
  • B. Hypertension only
  • C. Rapid relief of angina
  • D. Prolonged effect
    Correct answer: C. Rapid relief of angina

47. Patient with gastroparesis may benefit from:

  • A. Enteric-coated capsule
  • B. Rectal or parenteral route
  • C. Hard tablets
  • D. Oral suspension
    Correct answer: B. Rectal or parenteral route

48. Orally administered insulin is ineffective because:

  • A. It dissolves too fast
  • B. It is destroyed by gastric enzymes and acid
  • C. It cannot be absorbed in the lungs
  • D. It tastes bitter
    Correct answer: B. It is destroyed by gastric enzymes and acid

49. Which dosage form allows easy dose titration?

  • A. Oral liquid
  • B. Extended-release capsule
  • C. Chewable tablet
  • D. Enteric-coated pill
    Correct answer: A. Oral liquid

50. The ultimate goal of oral drug delivery is to:

  • A. Avoid prescription
  • B. Increase compliance and achieve therapeutic plasma concentration
  • C. Replace all other routes
  • D. Use only generics
    Correct answer: B. Increase compliance and achieve therapeutic plasma concentration

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