Top 350+ Solved Biopharmaceutics and Pharmacokinetics MCQ Questions Answer

From 376 to 389 of 389

Q. A hydrophilic medicinal agent has

a. Low ability to penetrate through the cell membrane lipids

b. Easy permeation through the blood-brain barrier

c. Penetrate through membranes by means of endocytosis

d. High reabsorption in renal tubules

  • a. Low ability to penetrate through the cell membrane lipids

Q. Biological barriers include all except:

a. Renal tubules

b. Cell membranes

c. Capillary walls

d. Placenta

  • a. Renal tubules

Q. Blood Brain Barrier is maximum permeable to

a. Na+

b. C02

c. Cl

d. K+

  • b. C02

Q. If a CNS drug is extensively ionized at pH of blood it will

a. Penetrate the blood brain barrier slowly

b. Penetrate the blood brain barrier rapidly

c. Not penetrate blood brain barrier

d. Be eliminated slowly

  • a. Penetrate the blood brain barrier slowly

Q. 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

  • a. Drug size (diffusion constant)

Q. 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

  • a. 0.693 *Vd / C1

Q. The procedure of transporting a drug from the bloodstream to tissues is called as

a. Absorption

b. Dissolution

c. Distribution

d. Elimination

  • c. Distribution

Q. …………..it represents the degree to which a drug is distributed in body tissue rather than

a. Volume of distribution (YD)

b. Effect of distribution

c. Area of distribution

d. None of the above

  • a. Volume of distribution (YD)

Q. It is defined as the distribution of a drug between plasma and the rest of the body after oral orparenteral dosing.

a. Volume of distribution (VD)

b. Apparent volume of drug distribution

c. Phagocytosis

d. None of the above

  • b. Apparent volume of drug distribution

Q. The drugs having molecular size …………..easily cross capillary membrane.

a. <500-600d

b. < 100-200 d

c. <300-600d

d. <90M600d

  • a. <500-600d

Q. Fat is act as reservoir for……………………… Drugs

a. Highly water soluble

b. Lower lipid soluble

c. Highly lipid soluble

d. Lower lipid soluble

  • c. Highly lipid soluble

Q. If distribution of drug is slower than process of biotransformation and elimination

a. It will cause high blood level of drug

b. It will cause low blood level of drug

c. Cause failure to attain diffusion equilibrium

d. None of the above

  • c. Cause failure to attain diffusion equilibrium
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