Top 350+ Solved Biopharmaceutics and Pharmacokinetics MCQ Questions Answer

From 1 to 15 of 389

Q. ……………is located at the sertoli-sertoli cell junction.

a. Blood testis barrier

b. Blood CSF barrier

c. Blood cellular barrier

d. All of the above

  • a. Blood testis barrier

Q. The Binding Order of drug to tissue is…………………

a. Kidney > Liver > Lungs > Muscle

b. Muscle > Kidney > Lungs > Liver

c. Liver > Kidney > Lungs > Muscle

d. Liver > Lungs > Kidney > Muscle

  • c. Liver > Kidney > Lungs > Muscle

Q. …………………in lipophilicity increases the extend of binding.

a. Increase

b. Decrease

c. Constant

d. None of the above

  • a. Increase

Q. 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

  • b. sink condition

Q. The loading dose of a drug is based upon the

a. time taken for complete elimination

b. percentage of drug excreted unchanged in urine

c. percentage of drug bound to plasma protein

d. apparent volume of distribution and the desired drug concentration in plasma

  • d. apparent volume of distribution and the desired drug concentration in plasma

Q. The volume of distribution of drugs is:

a. An expression of total body volume

b. A measure of total fluid volume

c. A relationship between the total amount of drug in the body and the concentration of the drug in the blood

d. Proportional to bioavailability of the drug

  • c. A relationship between the total amount of drug in the body and the concentration of the drug in the blood

Q. The volume of distribution (Vd) relates:

a. Single to a daily dose of an administered drug

b. An administered dose to a body weight

c. An unchanged drug reaching the systemic circulation

d. The amount of a drug in the body to the concentration of a drug in plasma

  • d. The amount of a drug in the body to the concentration of a drug in plasma

Q. Movement of drug across the membrane is called as

a. Symport

b. Antiport

c. Drug transport

d. Absorption

  • c. Drug transport

Q. Which of the following is known as Tamoxifen binding site?

a. Site I

b. Site II

c. Site III

d. Site IV

  • d. Site IV

Q. Which of the following drug selectively bound to extravascular tissues?

a. Warfarin

b. Diazepam

c. Digitoxin

d. Chloroquin

  • d. Chloroquin

Q. Plasma Protein binding …………..the volume of distribution of drugs.

a. increases

b. decreases

c. no change

d. none of the above

  • b. decreases

Q. Following intravenous administration, drugs are distributed fastest to:

a. the skin, kidney, and brain

b. the liver, kidney, and brain

c. the liver, adipose, and brain

d. the liver, kidney, and adipose

  • b. the liver, kidney, and brain

Q. …………is the tight junction between sertoli cells.

a. BBB

b. placental barrier

c. blood-testis barrier

d. endothelial barrier

  • c. blood-testis barrier

Q. Distribution is……………..

a. irreversible process

b. dynamic equilibrium process

c. Both (a) & (b)

d. none of the above

  • b. dynamic equilibrium process

Q. A drug reverses plasma-protein binding is often referred as……..

a. displacer

b. solvate

c. carrier substance

d. protein hydrolysate

  • a. displacer
Subscribe Now

Get All Updates & News