Pharmaceutics I Final Exam (2025)

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Last updated 6:11 PM on 8/25/26
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48 Terms

1
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A drug substance is known to degrade by the stomach acid. Which of the following dosage forms is preferred in such a situation?

Enteric coated tablet dosage form

2
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How do you define BCS Class I drugs?

High permeability, high solubility

3
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<p>If ‘ABC’ in the following picture is a pile of powder created on a surface as the powder was freely fallen from a funnel, which one is the angle of repose?</p>

If ‘ABC’ in the following picture is a pile of powder created on a surface as the powder was freely fallen from a funnel, which one is the angle of repose?

θ2

4
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Zinc chloride can provide a pair of electrons to form a coordination covalent bond. Therefore, zinc chloride can be called

a base according to Lewis theory

5
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Water and alcohols can be considered __________ solvents?

amphiprotic

6
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<p>Calculate the buffer capacity of a pharmaceutical buffer at pH 6.3. The Ka value is 1.51 × 10–6. The buffer contains 0.2 M conjugate acid and 0.5 M conjugate base. [</p>

Calculate the buffer capacity of a pharmaceutical buffer at pH 6.3. The Ka value is 1.51 × 10–6. The buffer contains 0.2 M conjugate acid and 0.5 M conjugate base. [

0.302

7
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What is the flux in mg/cm2/sec if 0.2 mg of a drug diffuses through a cross-sectional

area of 0.008 cm2 in 20 seconds at 25 °C?

1.25 mg/cm2/sec

8
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Noyes-Whitney equation is used to determine this parameter.

Drug dissolution

9
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<p>What type of chemical degradation is apparent from the following reaction?</p>

What type of chemical degradation is apparent from the following reaction?

Hydrolysis

10
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A complex reaction that occurs through a series of chain reactions via a free radical mechanism is called ______________.

auto-oxidation

11
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What is the true function of synergists in pharmaceutical preparations?

To increase the activity of antioxidants.

12
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All of the following EXCEPT this one are chemical methods of drug degradation.

Polymorphism

13
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Which one is NOT true for molecularity and order of a reaction?

Molecularity must be experimentally determined.

14
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<p>A drug formulation initially contained 225 mmol/liter of the drug. It was tested under the accelerated stability testing and found to contain 100 mmol/liter after 45 days. </p><p>Calculate the half-life of the degradation process if it follows first order kinetics.</p>

A drug formulation initially contained 225 mmol/liter of the drug. It was tested under the accelerated stability testing and found to contain 100 mmol/liter after 45 days.

Calculate the half-life of the degradation process if it follows first order kinetics.

38.5 days

15
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A solid oral dosage form is evaluated for real time stability studies at ___________.

25 °C/60% RH

16
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Which of the following statements correctly explains chemisorption?

It is when adsorption occurs due to the formation of chemical bonds.

17
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What type(s) of ion(s) are adsorbed on the true surface of an adsorbent?

Only potential determining ions

18
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How would you express Newton’s Law of Flow?

Shearing stress is proportional to the rate of shear.

19
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Describe the characteristic of a thixotropic system.

Thixotropy offers easy pouring and spreading of medicines.

20
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Which of the following is the most electronegative atom?

Fluorine

21
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Water is considered to be a ____________ solvent.

polar

22
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Which of the following is true for a solution system with negative heat of solution?

Heat evolves during the dissolution process.

23
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<p>Arecoline is a weakly basic drug with a pKa of 8.23. You have a stock solution of 3.22 moles/liter of arecoline in sterile water for injection. The solubility of arecoline in water is 2.88 moles/liter. What would be the pH of precipitation of arecoline in the stock solution?</p>

Arecoline is a weakly basic drug with a pKa of 8.23. You have a stock solution of 3.22 moles/liter of arecoline in sterile water for injection. The solubility of arecoline in water is 2.88 moles/liter. What would be the pH of precipitation of arecoline in the stock solution?

9.16

24
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Which of the following statements is consistent with flocculated suspensions?

Particles in sediments are weakly bonded.

25
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The rate of sedimentation of a suspension is 4.31 × 10–4 cm/sec when the particle size is 3.9 μm.

What would be the rate of sedimentation if the particle size is reduced to 1.6 μm?

7.25 × 10–5 cm/sec

26
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<p>What is the contact angle between the liquid and the solid surface in the following picture?</p>

What is the contact angle between the liquid and the solid surface in the following picture?

>90°

27
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Which of the following instruments or methods use rollers to crush the disperse phase in preparing lyophobic colloids?

Colloid mills

28
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There are, on average, 30 monomers in each micelle in the association colloid you prepared recently. Therefore, “30” is known as the _________________ of this system.

aggregation number

29
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In which phase of clinical trial post marketing surveillance is conducted?

Phase IV

30
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Which of the following statements regarding drug absorption is correct?

Drug should exist in non-ionized and lipid soluble form.

31
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Which of the following cyclodextrins would you select to prepare intravenous solution of a hydrophobic drug?

Gamma cyclodextrin

32
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Glycerin procured from unverified source is often adulterated with _______________.

diethylene glycol

33
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Doctor recommended antiseptic solution to treat a mild throat infection. Which of the following preparations would you choose to localized drug effect over the throat region?

Gargles

34
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Which of the following statements regarding salt formation technique is NOT correct?

Salt decreases first pass metabolism of a drug.

35
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Which of the following ointment bases have the highest occlusive effect over the dry skin?

Oleaginous bases

36
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A semisolid preparation contains 30% drug suspended in poloxamer gel. Which of the following semisolid preparation it represents?

Paste

37
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Which of the following mechanisms is NOT involved in drug release from suppository preparations?

Evaporation

38
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Which of the following dosage forms avoid first pass metabolism completely?

Pessaries

39
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A nasal solution contains dextrose in its composition. What is the function of dextrose in the nasal solution?

Sweetener

40
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Which of the following mechanisms is present in olfactory region of nasal cavity to prevent drug entry to the brain?

P-glycoprotein efflux

41
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Which of following oral inhalation preparation requires forceful inhalation?

DPI

42
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A patient is undergoing severe/acute asthmatic attack. Which of following oral inhalation preparations is the most effective against it?

Nebulizer

43
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How many phases are present in a pMDI preparation that contain solution formulation? The solution formulation is miscible with liquid phase of the HFA propellant.

Two phases

44
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The volume ratio of oil to water in a given emulsion preparation is 45:55. If the emulsifier used in this preparation is hydrophilic in nature, the type of emulsion that will be formed most likely is ___________.

o/w type

45
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HLB system is used to classify ______________.

surfactants

46
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What is the primary advantage of preparing emulsions using bottle method?

Volatile oils can be used.

47
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Radioactivity occurs mainly due to a change ___________?

in the nucleus

48
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Which of the following nuclear reaction represents a nuclear fission?

[236] 92U → [131] 53I + [102] 39Y + 3n