Explore topic-wise MCQs in GPAT.

This section includes 925 Mcqs, each offering curated multiple-choice questions to sharpen your GPAT knowledge and support exam preparation. Choose a topic below to get started.

351.

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» B. Finger-like projections whose other name is villi
352.

Protein binding of drugs helps to maintain ……………for absorption of drugs.

A. non sink condition
B. sink condition
C. pKa
D. none of the above
Answer» C. pKa
353.

If drug have very small volume of distribution it is likely that the drug

A. Has short biological half life
B. Does not accumulate in various tissue and organ
C. Not bioavailable
D. will not be effective
Answer» C. Not bioavailable
354.

Absorption of poorly soluble drug is

A. diffusion rate limited
B. dissolution rate limited
C. both (a) & (b)
D. none of the above
Answer» C. both (a) & (b)
355.

Based on Henderson-Hasselbalch equation, at what pH value a weak acid would be 99.9% ionized?

A. At pH equivalent to pKa - 3
B. At pH equivalent to pKa + 3
C. At pH equivalent to pKa – 1
D. At pH equivalent to pKa + 1
Answer» C. At pH equivalent to pKa – 1
356.

The process of engulfing of particulate material is called

A. Pinocytosis
B. Phagocytosis
C. Convective transport
D. Facilitated diffusion
Answer» C. Convective transport
357.

Two most common protein involved in plasma protein binding are

A. Globulin and plasmin
B. Albumin and globulin
C. Fibrin and globulin
D. Plasmin and fibrin
Answer» C. Fibrin and globulin
358.

What is the perfusion rate?

A. The total volume of blood
B. The volume of blood that flows through the heart per unit time
C. The volume of blood that flows per unit time per unit volume of tissue
D. The volume of tissue that flows per unit time per unit area of a blood vessel
Answer» D. The volume of tissue that flows per unit time per unit area of a blood vessel
359.

Larger the size of the counterion, greater the solubility.

A. True
B. False
C. none
D. all
Answer» C. none
360.

Which of the following is not the characteristic of the carrier mediated transport system?

A. Energy dependent
B. Reach equilibrium
C. Metabolically inhibited
D. Structurally specific and saturable
Answer» C. Metabolically inhibited
361.

When the solvent in association with the drug is water, the solvate is known as

A. anhydrate
B. amorphous
C. hydrate
D. none of the above
Answer» D. none of the above
362.

If the bioavailability of test formulation is 80-120% of the reference standard, it is considered to bebioequivalent.

A. True
B. False
C. none
D. all
Answer» B. False
363.

The formula to calculate half life (t1/2) is

A. 0.693 *Vd / C1
B. 0.693 *Cl / Vd
C. 0.693 / Cl * Vd
D. 0.693 / Cl
Answer» B. 0.693 *Cl / Vd
364.

This is the equation for the calculation of creatinine clearance. Which age group does the Clcr = (140 – Age) W / 85 * Scr formula belong to?

A. 1-6 years
B. 1-20 years
C. Males above 20 years
D. Females above 20 years
Answer» E.
365.

Which of the following is not a mechanism for pharmacokinetic analysis?

A. Compartment analysis
B. Non compartment analysis
C. Physiologic modeling
D. Human model
Answer» E.
366.

Conjugation is:

A. Process of drug reduction by special enzymes
B. Process of drug oxidation by special oxidases
C. Coupling of a drug with an endogenous substrate
D. Solubilization in lipids
Answer» D. Solubilization in lipids
367.

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» E.
368.

To avoid bioavailability issues, the drug must have a minimum aqueous solubility of

A. 150%
B. 10%
C. 100%
D. 1%
Answer» E.
369.

What will be the particle size after micronization of drugs?

A. 1-10 micron
B. 10-20 micron
C. 20-30 micron
D. 1-5 micron
Answer» B. 10-20 micron
370.

In which of the following models the body is considered to be composed of several compartments?

A. Compartment model
B. Noncompartment model
C. Physiologic model
D. Human model
Answer» B. Noncompartment model
371.

Which of the following drugs are responsible for retinopathy?

A. Acidic drugs like imipramine
B. Basic drugs like imipramine
C. Halogenated hydrocarbons
D. Chloroquinine
Answer» E.
372.

Which cell make up the blood-brain barrier?

A. Squamous epithelium cells
B. Fat cells
C. Red blood cell
D. Endothelial cells
Answer» E.
373.

When the active transport system become saturated, the rate process become

A. Zero order
B. Second order
C. Pseudo first order
D. Pseudo zero order
Answer» B. Second order
374.

What is the relation between halogenated hydrocarbon and liver?

A. Halogenated hydrocarbon is a drug for liver problems
B. Halogenated hydrocarbon is nutrition for liver
C. Halogenated hydrocarbon causes hepatotoxicity
D. Halogenated hydrocarbon forms the bile juices in liver
Answer» D. Halogenated hydrocarbon forms the bile juices in liver
375.

Which tissue has the greatest capacity to biotransform of drugs?

A. Kidney
B. Lung
C. Liver
D. Skin
Answer» D. Skin
376.

Why emulsion dosage form for lipophilic drug proved better?

A. Easy manufacturing
B. The higher stability of the drug in emulsion form
C. Presented a large surface area of oil to the GIT for the absorption of the drug
D. Fast clearance from the plasma
Answer» D. Fast clearance from the plasma
377.

Which of the given drugs bind to Α1 globulin?

A. Steroidal drugs
B. Vitamins A, D, E, K
C. Ferrous ions
D. Carotenoids
Answer» B. Vitamins A, D, E, K
378.

Which of the following is used in solvent deposition method of enhancing bioavailability?

A. Freeze drying
B. Organic solvent
C. Inorganic clays like bentonite
D. Creating metastable polymorphs
Answer» C. Inorganic clays like bentonite
379.

What is pharmaceutic equivalence?

A. Two or more drug products contain the same labeled chemical substance in the same amount
B. Two or more drug products are identical in quality, purity, uniformity, disintegration, dissolution
C. Two or more drug products contain different labeled chemical substance giving the same therapeutic effect
D. Two or more drug products contain the same labeled chemical substance giving a different therapeutic effect
Answer» C. Two or more drug products contain different labeled chemical substance giving the same therapeutic effect
380.

The half life of a drug eliminated by first order elimination kinetics will be longer in individuals whohave an:

A. increased volume of distribution or increased clearance
B. increased volume of distribution or decreased clearance
C. decreased volume of distribution or increased clearance
D. decreased volume of distribution or decreased clearance
Answer» C. decreased volume of distribution or increased clearance
381.

Bioavailability is expressed by formula

A. AUC IV / AUC oral
B. AUC ora1 X AUC IV
C. AUC ora1 / AUC IV
D. None of the above
Answer» B. AUC ora1 X AUC IV
382.

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» B. Imipramine
383.

Half life of zero-order process is proportional to of drug.

A. initial concentration
B. final concentration
C. both (a) & (b)
D. none of the above
Answer» B. final concentration
384.

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» C. Neutral drugs
385.

………….is used to study gastric emptying.

A. Barium sulphate
B. Aluminum sulphate
C. Calcium sulphate
D. Aluminum hydroxide
Answer» B. Aluminum sulphate
386.

Which one of them is not a common form of excipients of drug manufacturing?

A. Diluents
B. Binders
C. Sweeteners
D. Essential oils
Answer» E.
387.

Which one of the following factor related to protein-drug binding is not related to drug interactions with the binding site?

A. Competition between the drug and the binding site
B. Competition between drugs and normal body constituents
C. Allosteric changes in a protein molecule
D. Inter subject variation
Answer» E.
388.

Displacement is significant when, the displaced drug is more than protein bound.

A. 50%
B. 95%
C. 10%
D. 1%
Answer» C. 10%
389.

This is the equation for the calculation of creatinine clearance. Which age group does the Clcr = 0.48 H / Scr *[W/70]0.7 formula belong to?

A. 1-6 years
B. 1-20 years
C. Males above 20 years
D. Females above 20 years
Answer» C. Males above 20 years
390.

Which drug causes brown yellow discoloration of infant’s teeth?

A. Arsenicals
B. Tetracycline
C. Halogenated hydrocarbons
D. Lipophilic drug
Answer» C. Halogenated hydrocarbons
391.

When rate is independent of the reactant concentration, then it is called

A. zero order reaction
B. Pseudo zero order reaction
C. First order reaction
D. Second order reaction
Answer» B. Pseudo zero order reaction
392.

The rate of drug transport across a cell membrane by lipid diffusion depends on all of the followingexcept

A. Drug size (diffusion constant)
B. Surface area of absorption
C. Lipid partition coefficient
D. Density of tr
Answer» B. Surface area of absorption
393.

The ability of liver to excrete drug in bile is expressed by………

A. hepatic clearance
B. biliary clearance
C. non-renal clearance
D. renal clearance
Answer» C. non-renal clearance
394.

Which is the other name of “cell eating”?

A. Transcytosis
B. Phagocytosis
C. Pinocytosis
D. Endocytosis
Answer» C. Pinocytosis
395.

Which of the following is not an approach for overcoming bioavailability problems?

A. Pharmaceutic approach
B. Pharmacokinetic approach
C. Biologic approach
D. Partition coefficient approach
Answer» E.
396.

Which of the following factors for protein drug binding is a drug interaction factor?

A. Competition between drugs for the binding site
B. Age
C. Physicochemical characteristics of a drug
D. Physicochemical characteristics of the protein or binding agent
Answer» B. Age
397.

The occurrence of food in the GI tract can affect the drug bioavailability from an oral drug product.The above give statement is?

A. True
B. False
C. Both of the above
D. None of the above
Answer» B. False
398.

Bioavailability from IV route is……%

A. 10
B. 100
C. 1000
D. 10000
Answer» C. 1000
399.

Absorption of drugs can be categorized into 2 classes, physicochemical properties of drugs and Dosage form of the drug, on the basis of drug dissolution.

A. True
B. False
C. none
D. all
Answer» B. False
400.

Under compartment modeling, Wegner-Nelson-Method involves

A. Determination of absorption rate constant (Ka) from %ARA Vs time curve
B. Determination of elimination rate constant (Ka) from % ARA Vs time curve
C. Determination of absorption rate constant (Ke) from %ARA •Vs Concentration curve
D. Determination of plasma half life
Answer» B. Determination of elimination rate constant (Ka) from % ARA Vs time curve