Chapter 9: Drug metabolism and elimination

Rang & Dale's Pharmacology by Humphrey P. Rang

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Chapter 9: Drug metabolism and elimination

 

Complete Chapter Questions With Answers

 

Sample Questions Are Posted Below

 

MULTIPLE CHOICE

 

  1. Hepatic cytochrome P450 drug-metabolizing enzymes are primarily found in

 

  1. cell nuclei
  2. plasma membranes
  3. the cytoplasm
  4. the smooth endoplasmic reticulum
  5. mitochondria

 

Answer d: the smooth endoplasmic reticulum

 

  1. Phase II drug metabolism

 

  1. includes hydrolytic reactions
  2. produces low molecular weight products
  3. usually forms inactive metabolites
  4. takes place mainly in the kidneys
  5. requires NADPH as a cofactor

 

Answer c: usually forms inactive metabolites

 

  1. Ketoconazole produces non-competitive inhibition of cytochrome P450 by

 

  1. binding to the ferric form of heme iron
  2. binding to the active site of the enzyme
  3. causing enzyme autolysis
  4. oxidizing NADPH
  5. binding covalently to the P450 protein

 

Answer a: binding to the ferric form of heme iron

 

  1. In first-order drug elimination

 

  1. drug half-life is directly proportional to drug concentration
  2. the rate of elimination is directly proportional to drug concentration
  3. drug clearance is directly proportional to plasma drug concentration
  4. the rate of elimination is constant
  5. the rate of elimination is unpredictable

 

Answer b: the rate of elimination is directly proportional to drug concentration

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