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590+ Biopharmaceutics and Pharmacokinetics Solved MCQs

These multiple-choice questions (MCQs) are designed to enhance your knowledge and understanding in the following areas: Bachelor of Pharmacy (B. Pharma) .

Chapters

Chapter: Absorption
151.

The deleterious effect of various coatings on drug dissolution is shown in orders below. Which one of them is the correct order?

A. Enteric coat > sugar coat > nonenteric film coat
B. Enteric coat > nonenteric film coat > sugar coat
C. Nonenteric film coat > sugar coat > enteric coat
D. Sugar coat > enteric coat > nonenteric film coat
Answer» A. Enteric coat > sugar coat > nonenteric film coat
152.

Which of the following will be an example of an organic suspending agent?

A. CMC
B. MC
C. Acacia
D. Carbowaxes
Answer» C. Acacia
153.

Which one of these is not a mechanism of the working of surfactants?

A. Promote wetting by increasing the effective surface area
B. Helps in the dissolution of drug
C. Better membrane contact of the drug
D. Decrease membrane permeability
Answer» D. Decrease membrane permeability
154.

PABA complex is used for the enhancement of ______________

A. Enhanced chelation
B. Enhanced dissolution
C. Enhanced membrane permeability
D. Enhanced lipophilicity
Answer» D. Enhanced lipophilicity
155.

The concentration of colorant does not affect the drug solubility.

A. True
B. False
C. none
D. all
Answer» B. False
156.

Suspending agent and some sugars can be used as viscosity imparters.

A. True
B. False
C. none
D. all
Answer» A. True
157.

According to the pH-partition hypothesis which one of the given options doesn’t govern the absorption?

A. The molecular size of the drug
B. PH at the absorption site
C. Lipid solubility of unionized drugs
D. Dissociation constant
Answer» A. The molecular size of the drug
158.

If the pH of either side of the membrane is different, then the compartment whose pH favours greater ionization will have less amount of drug.

A. True
B. False
C. none
D. all
Answer» B. False
159.

Which of the following equations correct for Henderson-Hasselbach equation for weak acids?

A. PH = pKa – log (Unionized drug concentration /Ionized drug concentration)
B. PH = pKa – log (Ionized drug concentration/ Unionized drug concentration)
C. PH = pKa + log (Ionized drug concentration/ Unionized drug concentration)
D. PH = pKa + log (Unionized drug concentration /Ionized drug concentration)
Answer» C. PH = pKa + log (Ionized drug concentration/ Unionized drug concentration)
160.

Which of the following equations correct for Henderson-Hasselbach equation for weak bases?

A. PH = pKa – log (Unionized drug concentration /Ionized drug concentration)
B. PH = pKa – log (Ionized drug concentration/ Unionized drug concentration)
C. PH = pKa + log (Ionized drug concentration/ Unionized drug concentration)
D. PH = pKa + log (Unionized drug concentration /Ionized drug concentration)
Answer» D. PH = pKa + log (Unionized drug concentration /Ionized drug concentration)
161.

What is the pH range of the stomach?

A. 1-4
B. 5-8
C. 1-3
D. 1-8
Answer» C. 1-3
162.

What is the pH range of the intestine?

A. 4-5
B. 1-3
C. 1-8
D. 5-8
Answer» D. 5-8
163.

Acids in the pKa range 2.5-7.5 are greatly affected by changes in pH making their absorption pH dependent.

A. True
B. False
C. none
D. all
Answer» A. True
164.

Which one of these is an example of a strong acid drug?

A. Diazepam
B. Ibuprofen
C. Cromolyn
D. Aspirin
Answer» C. Cromolyn
165.

Which one of these is not an example of a basic drug with pKa range 5-11?

A. Cromolyn
B. Imipramine
C. Amitriptyline
D. Chloroquine
Answer» A. Cromolyn
166.

Example of a drug which has PKa > 11 is ________

A. Cromolyn
B. Imipramine
C. Amitriptyline
D. Mecamylamine
Answer» D. Mecamylamine
167.

What should be the range of oil/water partition coefficient of any drug?

A. 1-2
B. 3-4
C. 2-3
D. 1-3
Answer» A. 1-2
168.

Ibuprofen a weak acid, in the stomach will be present in which of the given form?

A. Ionized form mostly
B. Non-ionized form mostly
C. Half ionized and half no ionized
D. Will form aggregate
Answer» B. Non-ionized form mostly
169.

Nitrazepam a weak base, will be in which form in the stomach?

A. Ionized form mostly
B. Non-ionized form mostly
C. Half ionized and half no ionized
D. Will form aggregate
Answer» A. Ionized form mostly
170.

All drugs which are weak acids or acidic in nature will be in a unionized form in the plasma.

A. True
B. False
C. none
D. all
Answer» B. False
171.

Heroin with pKa 7.8 will be in which form in intestinal pH?

A. Ionized form mostly
B. Unionized form mostly
C. Half ionized and half no ionized
D. Will form aggregate
Answer» B. Unionized form mostly
172.

Which one of these options is not one of the limitations of pH-partition theory?

A. Presence if virtual membrane pH
B. Absorption of ionized drugs
C. Influence of GI surface area
D. Dissolution rate
Answer» D. Dissolution rate
173.

A microclimate pH, different from the luminal pH exists at the membrane surface.

A. True
B. False
C. none
D. all
Answer» A. True
174.

According to the pH-partition theory which form of the drug gets absorbed mostly?

A. Hydrated form
B. Aggregated form
C. Ionised
D. Unionised
Answer» D. Unionised
175.

What helps the ionized drug molecules to pass through the cell membrane passively?

A. Different pH
B. Polar group
C. Large lipophilic group
D. Hydration
Answer» C. Large lipophilic group
176.

Acidic drugs are best absorbed through the stomach and basic drugs are best absorbed through the intestine.

A. True
B. False
C. none
D. all
Answer» A. True
177.

What could be the reason that irrespective of pH any drug gets absorbed mostly from the intestine?

A. More surface area
B. Long residence time
C. Large surface area and long residence time
D. Large surface area, long residence time, basic pH
Answer» C. Large surface area and long residence time
178.

Drug having a small partition coefficient can rapidly penetrate the lipid membrane but diffusion through the unstirred water layer is a rate-limiting step.

A. True
B. False
C. none
D. all
Answer» B. False
179.

What are the major stability problems which result in poor bioavailability of any orally administered drugs?

A. Acidic degradation
B. Degradation by salivary amylase
C. Degradation of the drug in inactive form
D. Interaction with the excipients and degradation in an inactive form
Answer» D. Interaction with the excipients and degradation in an inactive form
180.

What is the mean length of GIT?

A. 350 cm
B. 200cm
C. 400cm
D. 450cm
Answer» D. 450cm
181.

The entire length of the GI is lined by ___________

A. Blood vessels
B. Nerves
C. Mucopolysaccharides
D. No lining direct contact with the cell
Answer» C. Mucopolysaccharides
182.

Which drugs get absorbed in the stomach mostly?

A. Basic drugs
B. Acidic Drugs
C. Neutral drugs
D. No drug gets absorbed in the stomach
Answer» B. Acidic Drugs
183.

Which drugs gets mostly absorbed from the mouth?

A. Acidic drugs and lipophilic drugs
B. Lipophilic drugs and neutral drugs
C. Neutral drugs and lipophilic drugs
D. Lipophilic, neutral, basic drugs
Answer» A. Acidic drugs and lipophilic drugs
184.

From the surface of villi protrude smaller projection known as __________

A. Microvilli
B. Villus
C. Fingers
D. Cilia
Answer» A. Microvilli
185.

Which of the following sentences will be the actual definition of folds of Kerckring?

A. Folds of the intestinal mucosa
B. Finger-like projections whose other name is villi
C. Protruding surface from the villi
D. Cilia over the surface of villi
Answer» A. Folds of the intestinal mucosa
186.

Which one of the following is not a characteristic for the small intestine?

A. Peristaltic movement
B. Long transit time
C. High permeability
D. PH 4-9
Answer» D. PH 4-9
187.

How can we increase the time of gastric emptying?

A. By drinking a lot of water
B. By taking a drug in empty stomach
C. By taking the drug after food
D. Cannot increase the time of gastric emptying at all
Answer» C. By taking the drug after food
188.

What is gastric emptying rate?

A. The time required for the gastric contents to empty into the small intestine
B. Time is taken for half of the contents in the stomach to empty
C. The speed at which the stomach contents empty into the intestine
D. There is no such term
Answer» C. The speed at which the stomach contents empty into the intestine
189.

How can we study the gastric emptying of a given drug?

A. By mixing the colour with the drug
B. Waiting for the subject man to throw-up
C. Tagging the drug with a radioisotope and scanning the stomach
D. Waiting for the patient to pass feces
Answer» C. Tagging the drug with a radioisotope and scanning the stomach
190.

Up to how much the microvilli in the small intestine increases the relative surface area of the small intestine?

A. 3 times
B. 30 times
C. 100 times
D. 600 times
Answer» D. 600 times
191.

What is the main role of the large intestine?

A. Absorption of water and electrolytes
B. Absorption of minerals
C. Absorption of glucose
D. Absorption of only water
Answer» A. Absorption of water and electrolytes
192.

The liver is the major site of drug metabolism.

A. True
B. False
C. none
D. all
Answer» A. True
193.

In infants, the gastric pH is quite low.

A. True
B. False
C. none
D. all
Answer» B. False
194.

The passage from the stomach to the small intestine is called gastric emptying.

A. True
B. False
C. none
D. all
Answer» A. True
195.

Which one is the sublingual route?

A. Drug placed between cheek and gum
B. Drug place between the tongue and upper palate
C. Drug placed under the tongue
D. Drug crushed and placed under the tongue
Answer» C. Drug placed under the tongue
196.

Which one of the following is the buccal route?

A. Drug placed between cheek and gum
B. Drug place between the tongue and upper palate
C. Drug placed under the tongue
D. Drug crushed and placed under the tongue
Answer» A. Drug placed between cheek and gum
197.

Which one of the following is not an advantage of sublingual or buccal administration?

A. Rapid absorption and higher blood levels
B. No first-pass hepatic metabolism
C. No degradation of drugs
D. Limited surface area
Answer» D. Limited surface area
198.

Which is the largest organ of the human body?

A. Liver
B. Stomach
C. Skin
D. Lungs
Answer» C. Skin
199.

What is the principal barrier for the drugs on the topical application?

A. The Dermis
B. The subcutaneous fat tissue
C. The stratum corneum
D. The blood vessels below the skin
Answer» C. The stratum corneum
200.

Which of the following decreasing order of blood flow rate through the muscular tissue is in the right order?

A. Arm > thigh > buttocks
B. Arm > buttocks > thigh
C. Buttocks > thigh > arm
D. Thigh > arm > buttocks
Answer» A. Arm > thigh > buttocks

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