1. LONGITUDNAL SECTION OF KIDNEY 09-12-20101KLECOP, Nipani

2. DEFINITION OF PHARMACOKINETICS AND PHARMACODYNAMICS

4. Renal Excretion Glomerular filtration depends on:  Renal blood flow & GFR; direct relationship  Plasma protein binding; only free unbound drugs are filtered Tubular Secretion in the proximal renal tubule mediates raising drug concentration in PCT lumen Organic anionic & cationic transporters (OAT & OCT) mediate active secretion of anionic & cationic drugs Passive diffusion of uncharged drugs Facilitated diffusion of charged & uncharged drugs Penicillin is an example of actively secreted drugs 4

5. Renal Excretion Tubular re-absorption in DCT: Because of water re-absorption, urinary D concentration increases towards DCT favoring passive diffusion of un-ionized lipophillic drugs It leads to lowering urinary drug concentration o Urinary pH trapping: Chemical adjustment of urinary pH can inhibit or enhance tubular drug reabsorption For example, aspirin overdose can be treated by urine alkalinization with Na Bicarbonate (ion trapping) and increasing urine flow rate (dilution of tubular drug concentration) Ammonium chloride can be used as urine acidifier for basic drug overdose treatment 5

6. Drug Elimination  Pulmonary excretion of drugs into expired air:  Gases & volatile substances are excreted by this route  No specialized transporters are involved  Simple diffusion across cell membrane predominates. It depends on: Drug solubility in blood: more soluble gases are slowly excreted Cardiac output rise enhance removal of gaseous drugs Respiratory rate is of importance for gases of high blood solubility  Biliary excretion of few drugs into feces o Such drugs are secreted from the liver into the bile by active transporters, and then into duodenum o Examples: digoxin, steroid hormones, some anticancer agents o Some drugs undergo enterohepatic circulation back into systemic circulation

7. CLEARANCE:- Is defined as the hypothetical volume of body fluids containing drug from which the drug is removed/ cleared completely in a specific period of time. Expressed in ml/min. CL = kV D, k: elimination rate constant CLEARANCE:- Is defined as the hypothetical volume of body fluids containing drug from which the drug is removed/ cleared completely in a specific period of time. Expressed in ml/min. CL = kV D, k: elimination rate constant 09-12-20107KLECOP, Nipani

8. Clearance It is ability of kidney, liver and other organs to eliminate drug from the bloodstream Units are in L/hr or L/hr/kg Used in determination of maintenance doses Drug metabolism and excretion are often referred to collectively as clearance The endpoint is reduction of drug plasma level Hepatic, renal and cardiac failure can each reduce drug clearance and hence increase elimination T 1/2 of the drug 8

9. TOTAL BODY CLEARANCE:- Is defined as the sum of individual clearances by all eliminating organs is called total body clearance/ total systemic clearance. TOTAL BODY CLEARANCE:- Is defined as the sum of individual clearances by all eliminating organs is called total body clearance/ total systemic clearance. 09-12-20109KLECOP, Nipani

10. Metabolism & Excretion Kinetics Elimination (metabolism + excretion) of most drugs follow first- order kinetics at therapeutic dose level  Amount of drug cleared in a given unit of time is directly proportional to the concentration of the drug according to Michaelis-Menten (linear) kinetics: Only few drugs (e.g., phenytoin, alcohol) show saturation clearance (Zero-order, non-linear) kinetics  Clearance mechanisms become saturated at therapeutic level, and clearance remain constant even with increased drug plasma level  SLOW ELIMINATION at therapeutic levels leads to toxic reactions E = Vmax x C k m + C

11. Minimum effective conc. Therapeutic success of a rapidly & completely absorbed drug. Therapeutic failure of a slowly absorbed drug. Subtherapeutic level Time Plasma Drug Conc.  Not only the magnitude of drug that comes into the systemic circulation but also the rate at which it is absorbed is important this is clear from the figure. 11

12. Loading Dose Loading Dose = Target Plasma C x VD What Is the is the loading dose required fro drug A if:  target concentration is 30 mg/L  VD is 0.75 L/kg, patients weight is 75 kg Answer VD = 0.75 L/kg x 75 kg = 56.25 L Target Conc. = 10 mg/L Dose = 30 mg/L x 56.25 L = 1659 mg

13. Half-life (t 1/2 ) Half-life: is a derived parameter, completely determined by volume of distribution and clearance. (Units = time) As Vd increases t1/2 increases

14. Maintenance Dose = CL x target steady state drug concentration The units of CL are in L/hr or L/hr/kg Maintenance dose will be in mg/hr

15. Steady-State Steady-state occurs after a drug has been given for approximately 4-5 t 1/2 At steady-state the rate of drug administration equals the rate of elimination Plasma concentration after each dose is approximately the same

16. Importance of Steady State (SS) At SS Rate in = Rate Out Steady state is reached usually within 4 – 5 half-lives at linear kinetics It is important for drug concentrations interpretation in:  Therapeutic Drug Monitoring (TDM)  Evaluation of clinical response

17. Dosing and Steady State Dosing: Administration of medication over time, so that therapeutic levels can be achieved. Steady-state: o drug accumulates and plateaus at a particular level o rate of accumulation determined by half life o reach steady state in about five times the elimination half-life

18. How Drugs Act: Pharmacodynamics

19. 2004-2005 Pharmacodynamics (how drugs work on the body) It is the study of biochemical and physiological effects of drugs and their mechanism of action at organ level as well as cellular level.

20. 2004-2005 Pharmacodynamics (how drugs work on the body) It is the study of biochemical and physiological effects of drugs and their mechanism of action at organ level as well as cellular level.

21. Do NOT impart new functions on any system, organ or cell Only alter the PACE of ongoing activity STIMULATION DEPRESSION REPLACEMENT CYTOTOXIC ACTION Principles of drug action

22. Majority of drugs interact with target biomolecules: Usually a Protein ENZYMES ION CHANNELS TRANSPORTERS RECEPTORS Targets of drug action

23. I- Ion Channels Direct Physical blocking of channel local anesthetic & amiloride Modulator Bind to the channel protein itself Ca channel blockers

24. II- Enzymes ChE inhibitors α-Methyl dopa

25. II- Enzymes (cont.) Drug acts as Substrate leading to reversible OR irreversible inhibition of enzyme  reversible inhibition of cholinesterase by neostigmine  Irreversible inhibition of cyclo-oxygenase by aspirin True/False substrate  L-DOPA converted into dopamine  α-methyldopa converted into α-methylnorepinephrine (false transmitter)

26. III- Carrier Molecules What is carrier molecule? Carrier protein molecules function to transport ions & small organic molecules (too polar to penetrate) across cell membranes.