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    Pharmaco Kinetics

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    Naghman Zuberi
    Pharmacokinetics is the study of how the body affects a drug over time. It involves absorption, distribution, metabolism, and excretion. Absorption depends on factors like route of administration and properties like lipid solubility. Distribution is affected by factors like blood flow and protein binding. Drugs are metabolized, often in the liver, through phase I and II reactions like oxidation and conjugation. Metabolites are usually more water soluble and excreted, mainly through urine but also bile and other routes. Changes in the elderly can impact absorption, distribution, and metabolism due to factors like decreased liver and kidney function.

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    Pharmaco Kinetics

    Uploaded by

    Naghman Zuberi
    100 views42 pages
    Pharmacokinetics is the study of how the body affects a drug over time. It involves absorption, distribution, metabolism, and excretion. Absorption depends on factors like route of administration and properties like lipid solubility. Distribution is affected by factors like blood flow and protein binding. Drugs are metabolized, often in the liver, through phase I and II reactions like oxidation and conjugation. Metabolites are usually more water soluble and excreted, mainly through urine but also bile and other routes. Changes in the elderly can impact absorption, distribution, and metabolism due to factors like decreased liver and kidney function.

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    Drug Metabolism

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    Pharmacokinetics is the study of how the body affects a drug over time. It involves absorption, distribution, metabolism, and excretion. Absorption depends on factors like route of administration and properties like lipid solubility. Distribution is affected by factors like blood flow and protein binding. Drugs are metabolized, often in the liver, through phase I and II reactions like oxidation and conjugation. Metabolites are usually more water soluble and excreted, mainly through urine but also bile and other routes. Changes in the elderly can impact absorption, distribution, and metabolism due to factors like decreased liver and kidney function.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PPT, PDF, TXT or read online from Scribd
    Download as ppt, pdf, or txt
    100 views42 pages

    Pharmaco Kinetics

    Uploaded by

    Naghman Zuberi
    Pharmacokinetics is the study of how the body affects a drug over time. It involves absorption, distribution, metabolism, and excretion. Absorption depends on factors like route of administration and properties like lipid solubility. Distribution is affected by factors like blood flow and protein binding. Drugs are metabolized, often in the liver, through phase I and II reactions like oxidation and conjugation. Metabolites are usually more water soluble and excreted, mainly through urine but also bile and other routes. Changes in the elderly can impact absorption, distribution, and metabolism due to factors like decreased liver and kidney function.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PPT, PDF, TXT or read online from Scribd
    Download as ppt, pdf, or txt
    of 42

    Pharmacokinetics

    By: Naghman Zuberi

    Pharmacokinetics
    Pharmacokinetics is the study of drug disposition in the body and focuses on the changes in drug plasma concentration

    Pharmacokinetics
    Pharmacokinetics is dependent on: absorption, distribution , and elimination.

    Drug Absorption
    Drug absorption refers to the passage of drug molecules from the site of administration into the circulation. The process of drug absorption applies to all routes of administration, except for the topical route and intravenous administration, topical route -drugs are applied directly on the target tissue. intravenous administration - the drug is already in the circulation.

    Drug Absorption
    Drug absorption requires that drugs cross one or more layers of cells and cell membranes. Drugs injected into the subcutaneous tissue and muscle bypass the epithelial barrier and are more easily absorbed through spaces between capillary endothelial cells.

    Drug Absorption
    In the gut, lungs, and skin, drugs must first be absorbed through a layer of epithelial cells that have tight junctions. For this reason, drugs face a greater barrier to absorption after oral administration than after parenteral administration.

    Processes of Absorption
    Passive Diffusion: across a biologic barrier and into the circulation. Ficks Law: The rate of absorption is proportional to the drug concentration gradient across the barrier and the surface area available for absorption at that site.

    Processes of Absorption
    Lipid Diffusion: is a process in which the drug dissolves in the lipid components of the cell membranes. This process is facilitated by a high degree of lipid solubility of the drug. Aqueous diffusion: occurs by passage through aqueous pores in cell membranes. It is restricted to drugs with low molecular weights. Many drugs are too large to be absorbed by this process.

    Processes of Absorption
    Active transport: requires a carrier molecule and a form of energy , provided by hydrolysis of the terminal high-energy phosphate bond of ATP. Active transport can transfer drugs against a concentration gradient. Facilitated diffusion: also requires a carrier molecule, but no energy is needed. Thus drugs or substances cannot be transferred against a concentration gradient but diffuse faster than without a carrier molecule present.

    Effect of pH on Absorption
    Effect of pH on Absorption of Weak Acids and Bases: pH Plays a Vital Role in the Absorption of Drugs since most of the Drugs are Either Weak Acids or Weak Bases. The rate of Absorption affects the Distribution and Elimination of a Drug.

    Physiologic changes that affect Absorption of Drugs in the Elderly


    Increased gastric pH Decreased absorptive surface area Decreased gastric motility Delayed gastric emptying

    The absorption, distribution, biotransformation (metabolism), and excretionof a typical drug after its oral administration.

    DRUG DISTRIBUTION
    Drugs are distributed to organs and tissues via the circulation, diffusing into interstitial fluid and cells from the circulation. Most drugs are not uniformly distributed throughout Total body water, and some drugs are restricted to the Extracellular fluid or plasma compartment. Drugs with sufficient lipid solubility can simply diffuse through membranes into cells. Other drugs are concentrated in cells by the phenomenon of ion trapping Some drugs are actively transported into hepatic cells.

    Factors Affecting Distribution


    Organ Blood Flow: Rate of Drug Distribution is Directly Proportional to the Cardiac Output. Plasma Protein Binding: Almost all drugs are reversibly bound to plasma proteins, primarily albumin , but also lipoproteins, glycoproteins, and globulins, depends on the affinity of a particular drug for protein-binding sites and ranges from < 10% to as high as 99% of the plasma concentration.

    Factors Affecting Distribution


    Molecular Size: Molecular size is a factor affecting the distribution of extremely large molecules. Lipid Solubility: Lipid solubility is a major factor affecting the extent of drug distribution, particularly to the brain, where the BBB restricts the penetration of polar and ionized molecules. The barrier is formed by tight junctions between the capillary endothelial cells and also by the glial cells that surround the capillaries, which inhibit the penetration of polar molecules into brain neurons.

    Age Related Problems in Drug Distribution


    Decrease in total body water will lead to a much smaller volume of distribution for water soluble drugs. Conversely, increases in total body fat will result in a larger volume of distribution for lipid soluble drugs. These factors along with age-related changes in drug clearance, can have a profound impact on the eventual steady-state concentrations.

    Age Related Problems in Drug Distribution


    If the patient is malnourished (which is often encountered in the elderly), a clinically significant increase in free drug serum concentration may occur. The binding affinity of albumin may also decrease with age, which may also increase free fractions of highly bound drugs.

    DRUG BIOTRANSFORMATION
    Biotransformation, or drug metabolism , is the enzyme-catalyzed conversion of drugs to their metabolites. Most drug biotransformation takes place in the liver. Drug-metabolizing enzymes are found in many other tissues, including the gut, kidneys, brain, lungs, and skin.

    Role of Drug Biotransformation


    The fundamental role of drug-metabolizing enzymes is to inactivate and detoxify drugs and other foreign compounds (xenobiotics) that can harm the body. Drug metabolites are usually more water soluble than is the parent molecule and, therefore, they are more readily excreted by the kidneys.

    No particular relationship exists between biotransformation and pharmacologic activity. Some drug metabolites are active, whereas others are inactive.

    Many drug molecules undergo attachment of polar groups, a process called conjugation, for more rapid excretion. Most conjugated drug metabolites are inactive, but a few exceptions exist.

    Formation of Active Metabolites


    Many pharmacologically active drugs are biotransformed to active metabolites. Prodrugs are administered as inactive compounds and then biotransformed to active metabolites because the prodrug is better absorbed than its active metabolite.

    First-Pass Biotransformation
    Drugs that are absorbed from the gut reach the liver via the hepatic portal vein before entering the systemic circulation. They are extensively converted to inactive metabolites during their first pass through the gut wall and iver, and have low bioavailability after oral administration. This phenomenon is called the first-pass effect. Drugs administered by the sublingual or rectal route undergo less first-pass metabolism and have a higher degree of bioavailability than do drugs administered by the oral route.

    Phase I Biotransformation
    It includes: oxidative, hydrolytic, and reductive reactions

    OXIDATIVE REACTIONS: Oxidative reactions are the most common type of phase I biotransformation. They are catalyzed by enzymes isolated in the microsomal fraction of liver homogenates (the fraction derived from the endoplasmic reticulum) and by cytoplasmic enzymes.

    HYDROLYTIC REACTIONS: Esters and amides are hydrolyzed by a variety of enzymes.

    REDUCTIVE REACTIONS: Reductive reactions are less common than are oxidative and hydrolytic reactions.

    Phase II Biotransformation
    In phase II biotransformation, drug molecules undergo conjugation reactions with an endogenous substance such as acetate , glucuronate , sulfate , or glycine Conjugation enzymes, which are present in the liver and other tissues, join various drug molecules with one of these endogenous substances to form water-soluble metabolites that are more easily excreted.

    GLUCURONIDE FORMATION: Glucuronide formation, the most common conjugation reaction, utilizes glucuronosyltransferases to conjugate a glucuronate molecule with the parent drug molecule.

    ACETYLATION: Acetylation is accomplished by Nacetyltransferase enzymes that utilize acetyl coenzyme A ( acetyl CoA) as a source of the acetate group.

    SULFATION: Sulfotransferases catalyze the conjugation of several drugs, including the vasodilator minoxidil and the potassium-sparing diuretic triamterene, whose sulfate metabolites are pharmacologically active.

    Changes in metabolism with age


    The liver is one of the major routes of drug elimination. There are several changes that can occur with advanced age that may affect drug metabolism: (1) Liver mass decreases (2) Hepatic blood flow decreases (Both liver mass and blood flow decrease about 40%) (3) Decreased first pass metabolism (4) Phase I metabolic reactions decline. (a) Hydroxylation (phenytoin) (b) Dealkylation (benzodiazepines) (c) Sulfide oxidation (chlorpromazine) (d) Hydrolysis (aspirin) (e) Nitro reduction (chloramphenicol)

    DRUG EXCRETION
    Excretion is the removal of drug from body fluids and occurs primarily in the urine. Other routes of excretion from thebody include in bile, sweat, saliva, tears, feces, breast milk, and exhaled air.

    Most drugs are excreted in the urine, either as the parent compound or as a drug metabolite. Drugs are handled by the kidneys in the same manner as are endogenous substances, undergoing processes of glomerular filtration, active tubular secretion, and passive tubular reabsorption. The amount of drug excreted is the sum of the amounts filtered and secreted minus the amount reabsorbed.

    Biliary Excretion and Enterohepatic Cycling


    Many drugs are excreted in the bile as the parent compound or a drug metabolite. Biliary excretion favors compounds with molecular weights that are higher than 300 and with both polar and lipophilic groups. Smaller molecules are excreted only in negligible amounts. Conjugation, particularly with glucuronate, increases biliary excretion.

    Biliary Excretion and Enterohepatic Cycling


    Numerous conjugated drug metabolites, including both the glucuronate and sulfate metabolites of steroids, are excreted in the bile. After the bile empties into the intestines, a fraction of the drug may be reabsorbed into the circulation and eventually return to the liver. This phenomenon is called enterohepatic cycling.

    Biliary Excretion and Enterohepatic Cycling


    Excreted conjugated drugs can be hydrolyzed back to the parent drug by intestinal bacteria, and this facilitates the drugs reabsorption. Biliary excretion eliminates substances from the body when the enterohepatic cycling is incomplete, that is, when some of the excreted drug is not reabsorbed from the intestine.

    Adverse Drug Reactions and Drug Interactions in the Elderly Patient


    ADR are 7 times more common in the elderly Account for 16% of hospital admission and 50% of medication related deaths

    Factors that Predispose Elderly to ADRs


    Drug accumulation secondary to reduced renal function Polypharmacy Greater use of drugs with a low therapeutic index ( i.e. digoxin) Inadequate supervision of long-term therapy Poor patient adherence

    Polypharmacy
    Definition : Taking a many of medications at the same time Beers 2005
    Average person over 65 takes an average of 4.5 prescription medications at a time plus 2 OTC medications

    References
    1. Goodman and Gillman Pharmacology 11th Edition. 2. Campion EW,deLabry LO, Glynn RJ. The effect of age on serum albumin in healthy males: Report from the Normative Aging Study. J Gerontol. 1988;43:M18M20. 3. Feely J, Coakley D. Altered pharmacodynamics in the elderly. Clin Geriatric Med. 1990; 6:269-283. 4. Greenblatt DJ, Sellers EM, Koch-Weser J. Importance of protein binding for the interpretation of serum or plama drug concentrations. J Clin Pharmacol. 1982;22:259263. 5. Lamy PP. Physiological changes due to age: pharmacodynamic changes of drug action and implications of therapy. Drugs Aging. 1991;1:385-404.

    6. Levy RA. Therapeutic inequivalence of pharmaceutical alternates. Amer Pharm. 1985; April: 28-39.
    7. Thoreson J. Drug Metabolism and Drug/Drug Interactions from a Geriatrics Perspective. Clin Ger. 1997; 5: 57-74.

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