Drug Metabolism and Prodrugs

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Presentation transcript:

Drug Metabolism and Prodrugs Drug metabolism is the transformation of foreign compounds ( xenobiotics) into water soluble derivatives which can easily eliminate via renal route.

Xenobiotics ( non essential exogenous, foreign compounds ) This applies particularly to chemical compounds which enter the organism and don't serve as nutrient or other essential factors. Xenobiotics can not be allowed to concentrate beyond limits in a living system, but must be eliminate by excretion. Xenobiotics metabolism appears as a logical evolutionary acquisition.

Drug metabolism may be regarded as detoxification processes in some cases. Not all metabolites are non toxic

Example

As a rule, the metabolism of xenobiotics takes place in two steps known as phase I & phase II reactions

Phase I ( functionalization reaction ) New polar groups such COOH, OH, SO3H or NH2 are introduced or unveiled from pre-existing function through oxidative, reductive or hydrolytic reactions.

Phase II ( conjugation reactions ) Link an endogenous solubilizing moiety either to the original drug (if polar function are already present) or to the phase I metabolite. Common solubilizing groups are glucuronic acid, various amino acids or sulphate grops. The conjugate molecule, being more polar and water-soluble, is usually excreted via the renal route

Effect of metabolism on the therapeutic activity of drugs

Conclusion Drug metabolism or biotransformation are the chemical reactions that are responsible for the conversion of drugs into other products within the body before and after they have reached their sites of action. Almost all of these reactions are enzyme catalyzed. A knowledge of the concepts of drug metabolism is useful in both the design of new drugs and the improvement of existing drugs.

Factors affecting drug metabolism Genetic factors Physiological factors Pharmaceutical factors Drug interactions

Biological half –life (t1/2) of various drugs Genetic factors Biological half –life (t1/2) of various drugs

Physiological factors

Pharmacodynamic factors The dose, the route and the frequency of administration of drugs can affect their metabolic profiles. Drugs given too frequently may overload the metabolic system available to it, leading to elevated blood and tissue levels of the drugs. The effect of protein binding also influences the metabolism

Drug interactions Phenobarbital stimulate the metabolism of Diphenylhydantoin. The half life of Chloropropamide, Diphenylhydantoin & Cyclophosphamide is increase in presence of Chloramphenicol. Plasma Concentration of anticoagulants such as Warfarin are reduced by simultaneous application of barbiturate

Phase I (Functionalization reactions Oxidations (electron removal, dehydrogenation and hydroxylation) Reduction ( electron donation, hydrogenation and removal of oxygen ) Hydrolytic reactions

Oxidation Reactions The main enzymes involved in the oxidation of xenobiotics called mixed – function oxidases or monooxygenases, found mainly in the liver but also occur to less extent in other tissues. Cytochrom P-450 ( CYP – 450 )

Major reactions of oxygenation catalyzed by cytochrome P450

Major reactions of oxygenation catalyzed by cytochrome P450

Oxidation reactions Carbon oxidation reaction a - Hydroxylation of saturated aliphatic carbon atoms b - Hydroxylation at activated SP3 carbon atoms c - Oxidation attack on unsaturated aliphatic systems d - Hydroxylation of aromatic rings N-oxygenation reactions S-oxidation reactions

Hydroxylation of saturated aliphatic carbon atoms Saturated aliphatic C-H bonds are normally metabolised by hydroxylation ( ω & ω-1 )

Enzymatic introduction of a hydroxyl group into cyclohexane ring generally occurs at C-3 or C-4 In human the trans-4-hydroxycyclohexyl product has been reported as a major metabolite of acetohexamide ( hypoglycemic agent )

Terodiline Aromatic p-hydroxylation predominate with R-isomer where as benzylic hydroxylation is preferred with S-isomer.

Hydroxylation at activated SP3 carbon atoms

Oxidation involving carbo-heteroatom system

N-dealkylation

Halogenated aliphatic derivatives

Oxidation attack on unsaturated aliphatic systems