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Cardiovascular System-Theme 1

           Dr. Fahad Azam
           Pharmacology and Therapeutics
THEME 1: BREATHLESSNESS AND
                 SWELLING (CCF)
•   CASE 1
•   A 64 years old male with heart failure was put on digoxin therapy in tablet form, formulated by XYZ
    pharmaceutical. Initially he was given 0.5mg 8 hourly for three days followed by 0.125mg/day.
    Simultaneously he was suffering from severe cough, fever and malaise, the physician after
    thorough investigations diagnosed him as a case of lower respiratory tract infection and prescribed
    100mgday doxycycline initially for one week which was further extended to 10 days. The patient
    suffered from diarrhea, doxycycline was discontinued, a course of metronidazole was given and
    patient got cured.
•
•    After few days patient presented with complaints of nausea, vomiting, fatigue, palpitations. The
    dose of digoxin was increased to 0.25 mg/day and he felt better.
•
•   After few years he was diagnosed for chronic renal failure, blood urea and creatinine were raised.
    He developed heart sinking and palpitation. On examination, the patient had an irregular pulse.
    ECG showed pulses bigeminy. Serum digoxin was 2.8 ng/ml. Digoxin therapy was stopped for three
    days. KCI was administered for few days. The plasma level was now repeated and was 1ng/ml. The
    dose of digoxin was adjusted to 0.125 mg /day. The patient became stable in a week.
LEARNING OBJECTIVES
1. Describe general principles of pharmacology, sources of drugs, routes of drug
   administration, Essential Drugs concept.
2. Describe drug transport across biological membranes.
3. Relate concepts of half life of drug, plasma protein binding drug and volume of
   distribution of drugs to its bioavailability.
4. Describe loading dose, steady state concentration, target concentration and
   maintenance concentration and bioequivalence of drugs.
5. Describe drug excretion, clearance, zero and first order kinetic of drugs.
6. Relate drug metabolism, factors affecting drug metabolism and its clinical
   significance.
7. Relate drug receptor concepts, antagonism, synergism, drug-receptor interaction
   and signaling mechanism of drugs.
8. Define relation between drug concentration and response and define drug
   response curves (graded and quantal).
9. Describe dose response curves, pharmacokinetic and pharmacodynamic drug
   interactions, drug toxicity, therapeutic index and therapeutic window.
Modes of Transport Across Biological Membranes

Mechanism          Direction                    Energy Required Carrier   Saturable
Passive diffusion Down gradient                 No              No        No
Facilitated        Down gradient                No              Yes       Yes
diffusion
Active transport   Against gradient             Yes             Yes       Yes
                   (concentration/electrical)
Drug permeation is dependent on:
• Fick’s law of Diffusion:
  – Solubility
  – Concentration gradient
  – Surface area
  – Vascularity
  – Thickness
Henderson-Hasselbalch equation

       [protonated]
 log ______________ = pKa -pH
      [unprotonated ]
• Drugs are either weak bases or weak acids
  (depending on their pKa) and can exist in
  either ionized or non ionized form (depending
  on their pKa and pH of the environment)
• Ionized = water soluble
• Non ionized = lipid soluble
• pKa is the intrinsic value of a drug, it does not
  change
• pKa is the pH at which the drug or molecule is
  50% ionized and 50 % non ionized
Clinical Application of Henderson-Hasselbalch
                       Equation

• Ionization increases renal clearance of Drugs
• Only free, unbound drug is filtered
• Both ionized and nonionized forms of drug are filtered
• Non ionized forms are reabsobred whereas ionized
  forms are non absorbed as they have a charge and
  cannot pass through lipid membranes (lipid insoluble)
• Ionized forms of drugs are “trapped” in the filtrate
Clinical Application of Henderson-Hasselbalch
                    Equation

• Both ionized and nonionized forms of drug are filtered
• Non ionized forms are reabsobred whereas ionized
  forms are non absorbed as they have a charge and
  cannot pass through lipid membranes (lipid insoluble)
• Ionized forms of drugs are “trapped” in the filtrate
• Acidification of urine increases ionization of weak
  bases  increases renal elimination
• Alkalinization of urine  increases ionization of weak
  acids  increases renal elimination
To Change Urinary pH
• Acidify: NH4Cl, Vitamin C, Cranberry juice
• Alkalinize: NaHCO3, Acetazolamide

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2003 cvs shifa permeation through biological membranes

  • 1. Cardiovascular System-Theme 1 Dr. Fahad Azam Pharmacology and Therapeutics
  • 2. THEME 1: BREATHLESSNESS AND SWELLING (CCF) • CASE 1 • A 64 years old male with heart failure was put on digoxin therapy in tablet form, formulated by XYZ pharmaceutical. Initially he was given 0.5mg 8 hourly for three days followed by 0.125mg/day. Simultaneously he was suffering from severe cough, fever and malaise, the physician after thorough investigations diagnosed him as a case of lower respiratory tract infection and prescribed 100mgday doxycycline initially for one week which was further extended to 10 days. The patient suffered from diarrhea, doxycycline was discontinued, a course of metronidazole was given and patient got cured. • • After few days patient presented with complaints of nausea, vomiting, fatigue, palpitations. The dose of digoxin was increased to 0.25 mg/day and he felt better. • • After few years he was diagnosed for chronic renal failure, blood urea and creatinine were raised. He developed heart sinking and palpitation. On examination, the patient had an irregular pulse. ECG showed pulses bigeminy. Serum digoxin was 2.8 ng/ml. Digoxin therapy was stopped for three days. KCI was administered for few days. The plasma level was now repeated and was 1ng/ml. The dose of digoxin was adjusted to 0.125 mg /day. The patient became stable in a week.
  • 3. LEARNING OBJECTIVES 1. Describe general principles of pharmacology, sources of drugs, routes of drug administration, Essential Drugs concept. 2. Describe drug transport across biological membranes. 3. Relate concepts of half life of drug, plasma protein binding drug and volume of distribution of drugs to its bioavailability. 4. Describe loading dose, steady state concentration, target concentration and maintenance concentration and bioequivalence of drugs. 5. Describe drug excretion, clearance, zero and first order kinetic of drugs. 6. Relate drug metabolism, factors affecting drug metabolism and its clinical significance. 7. Relate drug receptor concepts, antagonism, synergism, drug-receptor interaction and signaling mechanism of drugs. 8. Define relation between drug concentration and response and define drug response curves (graded and quantal). 9. Describe dose response curves, pharmacokinetic and pharmacodynamic drug interactions, drug toxicity, therapeutic index and therapeutic window.
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  • 5. Modes of Transport Across Biological Membranes Mechanism Direction Energy Required Carrier Saturable Passive diffusion Down gradient No No No Facilitated Down gradient No Yes Yes diffusion Active transport Against gradient Yes Yes Yes (concentration/electrical)
  • 6. Drug permeation is dependent on: • Fick’s law of Diffusion: – Solubility – Concentration gradient – Surface area – Vascularity – Thickness
  • 7. Henderson-Hasselbalch equation [protonated] log ______________ = pKa -pH [unprotonated ]
  • 8. • Drugs are either weak bases or weak acids (depending on their pKa) and can exist in either ionized or non ionized form (depending on their pKa and pH of the environment) • Ionized = water soluble • Non ionized = lipid soluble
  • 9. • pKa is the intrinsic value of a drug, it does not change • pKa is the pH at which the drug or molecule is 50% ionized and 50 % non ionized
  • 10. Clinical Application of Henderson-Hasselbalch Equation • Ionization increases renal clearance of Drugs • Only free, unbound drug is filtered • Both ionized and nonionized forms of drug are filtered • Non ionized forms are reabsobred whereas ionized forms are non absorbed as they have a charge and cannot pass through lipid membranes (lipid insoluble) • Ionized forms of drugs are “trapped” in the filtrate
  • 11. Clinical Application of Henderson-Hasselbalch Equation • Both ionized and nonionized forms of drug are filtered • Non ionized forms are reabsobred whereas ionized forms are non absorbed as they have a charge and cannot pass through lipid membranes (lipid insoluble) • Ionized forms of drugs are “trapped” in the filtrate • Acidification of urine increases ionization of weak bases  increases renal elimination • Alkalinization of urine  increases ionization of weak acids  increases renal elimination
  • 12. To Change Urinary pH • Acidify: NH4Cl, Vitamin C, Cranberry juice • Alkalinize: NaHCO3, Acetazolamide