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Contents​
• Metabolism (active --> inactive)​
• Prodrug (inactive --> active)​
• Drug with equally active metabolite (active --> active)​
• First Pass Metabolism (presystemic biotransformation)​
• Chemical pathway of Metabolism​
• Enzyme induction and Enzyme inhibition​
• Factors affecting Metabolism​
Metabolism
• Biotransformation means enzyme catalyzed biochemical transformation
of drugs within the living organism. ​
• The metabolites thus formed are much less lipid soluble, hence
not reabsorbed from the renal tubules and thus are finally excreted. ​
• The biotransformation of drugs, which is the more preferred term, occurs
mainly in liver, although kidney, intestine, adrenal cortex, lungs, placenta
and skin may also be involved to some extent. ​
• The dead tissues, like nails and hair are not involved in
drug biotransformation.​
Metabolism (active --> inactive)​
• This is usual case: e.g. Phenobarbitone (active metabolite)
is converted to hydroxy Phenobarbitone (inactive metabolite)​
Prodrug (inactive --> active)​
• ​It is useful when drug undergoes first pass metabolism
• E.g. L-Dopa (inactive) converts to Dopamine (active)​
Drug with equally active metabolite (active --> active)
• It is beneficial for long duration of action
• E.g. Diazepam (active) is converted to Oxazepam (active)
First Pass Metabolism
• All drugs taken orally, first of all, pass through GIT wall and then
through portal system, before reaching the systemic circulation.
• First-Pass Metabolism or the pre-systemic metabolism or the First-
Pass Effect means the drug metabolism occurring before the drug
enters the systemic circulation.
• The net result is the decreased bioavailability of the drug and
consequently a diminished therapeutic response, because a
significant amount of the drug is inactivated before reaching the
systemic circulation.
• The first-pass effect may be bypassed if the drug is administered
parenterally.
Chemical Pathways
• Phase I reactions
This are Degradative reactions, makes drug small and polar molecule
Includes oxidation, reduction and hydrolysis reactions
• Phase II reactions
This are synthetic reaction also called Conjugation
The metabolite formed are small, inactive and water soluble
Phase – I Reactions
• Oxidation
Microsomal
Non - microsomal
• Reduction
Microsomal
Non - microsomal
• Hydrolysis
Microsomal
Non - microsomal
Microsomal
This are enzymes located on SER, of the
Liver.This is also called Cytochrome P450
system of enzymes.
Non - Microsomal
This are enzymes from mitochondria,
cytoplasm, and plasma. Includes enzymes
like oxidase, transferase, amidase, etc.
Oxidation Reactions
• Aromatic/Aliphatic hydroxylation (addition of OH group)
• N/S Dealkylation or Oxidation
• Deamination or Sulfurization
• Cytoplasmic oxidation and Mitochondrial oxidation
Refer examples from H. L. Sharma
Reduction Reactions
• Nitro Reduction
• Azo Reduction
• Keto Reduction
Hydrolysis Reactions
• Very Rarely observed reaction
Phase – II: Conjugation
• Glucuronide Conjugation
• N – acetyl conjugation
• Sulfate Conjugation
• Amino acid Conjugation
• Methyl Conjugation
• Glutathione Conjugation
• Phosphate Conjugation
Glucuronide Conjugation
UDPGA (uridine diphosphate glucuronic acid)
Sulfate Conjugation
N - acetyl Conjugation
Enzyme Induction and Enzyme inhibition
• Some drugs, that have ability to induce the enzymes involved in
process of metabolism.
• While some others, have ability to inhibit the enzymes involved in
process of metabolism.
• This kind of drugs when administered can show toxicity or can reduce
the effect of other co-administered drugs.
• Hence Enzyme inducers reduce the effect of drugs by metabolizing
them at faster rate.
• And Enzyme inhibitors can result in sudden toxicity of other drug due
to inhibition of metabolism
Factors Affecting Metabolism
• Age
• Gender
• Species
• Race
• GeneticVariation
• Nutrition and Diet
• Disease
• Drug - Drug Interaction
To be Finished soon….

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Metabolism of drugs Pharmacokinetics

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  • 3. Contents​ • Metabolism (active --> inactive)​ • Prodrug (inactive --> active)​ • Drug with equally active metabolite (active --> active)​ • First Pass Metabolism (presystemic biotransformation)​ • Chemical pathway of Metabolism​ • Enzyme induction and Enzyme inhibition​ • Factors affecting Metabolism​
  • 4. Metabolism • Biotransformation means enzyme catalyzed biochemical transformation of drugs within the living organism. ​ • The metabolites thus formed are much less lipid soluble, hence not reabsorbed from the renal tubules and thus are finally excreted. ​ • The biotransformation of drugs, which is the more preferred term, occurs mainly in liver, although kidney, intestine, adrenal cortex, lungs, placenta and skin may also be involved to some extent. ​ • The dead tissues, like nails and hair are not involved in drug biotransformation.​
  • 5. Metabolism (active --> inactive)​ • This is usual case: e.g. Phenobarbitone (active metabolite) is converted to hydroxy Phenobarbitone (inactive metabolite)​ Prodrug (inactive --> active)​ • ​It is useful when drug undergoes first pass metabolism • E.g. L-Dopa (inactive) converts to Dopamine (active)​ Drug with equally active metabolite (active --> active) • It is beneficial for long duration of action • E.g. Diazepam (active) is converted to Oxazepam (active)
  • 6. First Pass Metabolism • All drugs taken orally, first of all, pass through GIT wall and then through portal system, before reaching the systemic circulation. • First-Pass Metabolism or the pre-systemic metabolism or the First- Pass Effect means the drug metabolism occurring before the drug enters the systemic circulation. • The net result is the decreased bioavailability of the drug and consequently a diminished therapeutic response, because a significant amount of the drug is inactivated before reaching the systemic circulation. • The first-pass effect may be bypassed if the drug is administered parenterally.
  • 7. Chemical Pathways • Phase I reactions This are Degradative reactions, makes drug small and polar molecule Includes oxidation, reduction and hydrolysis reactions • Phase II reactions This are synthetic reaction also called Conjugation The metabolite formed are small, inactive and water soluble
  • 8. Phase – I Reactions • Oxidation Microsomal Non - microsomal • Reduction Microsomal Non - microsomal • Hydrolysis Microsomal Non - microsomal Microsomal This are enzymes located on SER, of the Liver.This is also called Cytochrome P450 system of enzymes. Non - Microsomal This are enzymes from mitochondria, cytoplasm, and plasma. Includes enzymes like oxidase, transferase, amidase, etc.
  • 9. Oxidation Reactions • Aromatic/Aliphatic hydroxylation (addition of OH group) • N/S Dealkylation or Oxidation • Deamination or Sulfurization • Cytoplasmic oxidation and Mitochondrial oxidation Refer examples from H. L. Sharma
  • 10. Reduction Reactions • Nitro Reduction • Azo Reduction • Keto Reduction Hydrolysis Reactions • Very Rarely observed reaction
  • 11. Phase – II: Conjugation • Glucuronide Conjugation • N – acetyl conjugation • Sulfate Conjugation • Amino acid Conjugation • Methyl Conjugation • Glutathione Conjugation • Phosphate Conjugation
  • 12. Glucuronide Conjugation UDPGA (uridine diphosphate glucuronic acid) Sulfate Conjugation N - acetyl Conjugation
  • 13. Enzyme Induction and Enzyme inhibition • Some drugs, that have ability to induce the enzymes involved in process of metabolism. • While some others, have ability to inhibit the enzymes involved in process of metabolism. • This kind of drugs when administered can show toxicity or can reduce the effect of other co-administered drugs. • Hence Enzyme inducers reduce the effect of drugs by metabolizing them at faster rate. • And Enzyme inhibitors can result in sudden toxicity of other drug due to inhibition of metabolism
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  • 16. Factors Affecting Metabolism • Age • Gender • Species • Race • GeneticVariation • Nutrition and Diet • Disease • Drug - Drug Interaction
  • 17. To be Finished soon….