1. 1 Pharmacology Pharmacokinetics –Absorption –Distribution –Biotransformation (metabolism) –Excretion Pharmacodynamics –Receptor binding –Signal transduction –Physiologic effect

2. 2 Drug distribution The transport of a drug in the body by the bloodstream to its site of action Protein-binding Water soluble vs. fat soluble Blood-brain barrier Areas of rapid distribution: heart, liver, kidneys, brain Areas of slow distribution: muscle, skin, fat 59-291 Section 1, Lecture 3

3. 3 Circulation Interstitial fluid cells -most drugs not uniformly distributed throughout the total body water -can be trapped in interstitial fluid or in plasma - if sufficiently lipophilic (hydrophobic) can get into cells

4. 4 -maybe concentrated by ion trapping pH =2 pH =7.4 HAH + + A - Consider a drug with a pKa= 2 -actively transported into liver cells and biotrnasformed -intestines drugs (anticancer) are pumped from blood to lumen and excreted by the body’s natural detoxifying mechanisms

5. 5 Volume of Distribution V d the volume of fluid in which drug would need to be dissolved in order to have the same concentration in that volume as it does in plasma V (L) PLASMA 4 INTERSTITIAL FLUID 10 INTERCELLULAT FLUID 28 V d provides an indication of physiological distribution of a drug

6. 6 Calculation of the V d

7. 7 If V d = plasma volume or extracellular (interstitial) volume drug remains outside of cells (Plasma or interstitial fluid) If V d = total body water drug is evenly distributed (ie ethanol) 500mg/ 11.9 mg/L= 42 L If V d = >> total body water indicates drugs are concentrated in cells by ion trapping (500mg /2mg/L= 250L) Many weak bases have a large V d due to intracellular ion trapping in the cells. Intracellular pH is less than Plasma pH >> weak bases are more in ionized from inside the cells

8. 8 Factors Affecting Distribution Organ blood flow –Brain, heart, liver, kidney > skeletal muscle > skin, adipose tissue Plasma protein binding –Albumin; Drug binding to albumin ranges from 10% to 99% of plasma concentration –Alpha 1 acid glycoprotein –Corticosteroid binding globulin –Alb-DrugFree drugInterstitial fluid, cells –Albumin (plasma protein) binding is saturable. What does this mean?? Molecular size –High MW drugs stay only in plasma; Heparin Lipid solubility –Blood Brain Barrier restricts the penetration of polar and ionized molecules into brain neurons

9. 9 EXERCISE: A patient suffering from hyperalbumineuria requires 5 times the normal dose of an analgesic. Why? What kind of a V d would you expect this patient to have for this analgesic?

10. 10 Drug Biotransformation (Drug metabolism) Enzyme-catalyzed conversion of drugs to their inactive metabolites, more soluble forms, or a more potent metabolite Main purpose: To detoxify and inactive drugs and other foreign substances Liver (main site), Kidneys, lungs, plasma, intestinal mucosa Metabolites are usually more water soluble and excreted by kidneys Prodrugs are biotransfomed to active drugs –Prodrug is absorbed better than biotransformed First-pass biotransformation

11. 11 First-pass effect Inactivates many drugs Alternatives: Rectal or sublingual

12. 12 Phases of Drug transformation Phase I- create a chemical functional group on the drug that can be recognized by Phase-II enzymes. Product of phase I enzymes still have biological activity Phase II- no biological activity

13. 13 Phase I Biotransformation Oxidative reactions –Catalyzed by enzymes of microsomal fraction (ER) of liver Microsomal cytochrome P450 monooxygenase Hydrolytic reactions Reductive reactions

14. 14 Phase I reactions

15. 15 Monooxygenase reaction Microsomal cytochrome P450 monooxygenase system is a family of enzymes that biotransforms many drugs