Pharmacology Chapter on Absorption
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Pharmacology Chapter on Absorption

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Questions and Answers

What factors influence the rate and extent of drug absorption?

  • The age of the patient.
  • The environment where the drug is absorbed. (correct)
  • The time of day the drug is administered.
  • The body weight of the patient.
  • Which of the following is NOT a factor affecting drug absorption?

  • Bioavailability.
  • Route of administration.
  • Chemical characteristics of the drug.
  • Duration of treatment. (correct)
  • How does the route of administration impact drug absorption?

  • It alters the chemical structure of the drug.
  • It influences bioavailability. (correct)
  • It determines the patient’s adherence to medication.
  • It affects the patient's tolerance to the drug.
  • Which statement is true regarding the chemical characteristics of a drug?

    <p>They determine the drug's solubility and permeability.</p> Signup and view all the answers

    What is the relationship between absorption and bioavailability in drug administration?

    <p>Bioavailability can be influenced by the route of administration, which impacts absorption.</p> Signup and view all the answers

    What primarily determines the rate of blood flow to tissues?

    <p>Capillary structure</p> Signup and view all the answers

    Which factor is associated with capillary permeability?

    <p>Chemical nature of the drug</p> Signup and view all the answers

    Which aspect does NOT affect blood flow to tissues?

    <p>Lipid levels in the tissue</p> Signup and view all the answers

    What plays a critical role in determining how blood flows within capillaries?

    <p>Capillary structure</p> Signup and view all the answers

    Which of the following factors influences the effectiveness of a drug at the tissue level?

    <p>Rate of blood flow to tissues</p> Signup and view all the answers

    What is passive diffusion in the context of drug absorption from the gastrointestinal tract?

    <p>The drug moves from a region of high concentration to one of lower concentration.</p> Signup and view all the answers

    Which statement best describes the conditions under which passive diffusion of drugs occurs?

    <p>In any condition but it is more efficient when concentration gradients are significant.</p> Signup and view all the answers

    In which scenario would passive diffusion not effectively transport a drug?

    <p>When the drug is a large polar molecule.</p> Signup and view all the answers

    How does passive diffusion affect the rate of drug absorption?

    <p>It tends to increase absorption rate when there is a high concentration gradient.</p> Signup and view all the answers

    Which of the following factors does not influence passive diffusion of drugs?

    <p>The price of the medication.</p> Signup and view all the answers

    What effect does first-pass hepatic metabolism have on drug levels in systemic circulation?

    <p>It decreases the amount of unchanged drug entering the systemic circulation.</p> Signup and view all the answers

    What happens to a drug that is rapidly metabolized during first-pass hepatic metabolism?

    <p>The amount of unchanged drug entering systemic circulation is decreased.</p> Signup and view all the answers

    Which statement about the first-pass effect is true?

    <p>It primarily takes place in the liver or gut wall.</p> Signup and view all the answers

    Why is first-pass metabolism clinically significant?

    <p>It can influence dosage adjustments for drugs.</p> Signup and view all the answers

    In the context of first-pass hepatic metabolism, what is primarily affected?

    <p>The concentration of unchanged drug in systemic circulation.</p> Signup and view all the answers

    What effect does reversible binding of a drug to plasma proteins have?

    <p>It sequesters drugs in a non-diffusible form.</p> Signup and view all the answers

    Which mechanism is primarily affected by the binding of drugs to plasma proteins?

    <p>The transfer of the drug out of the vascular compartment.</p> Signup and view all the answers

    What is the consequence of drugs being sequestered in a non-diffusible form?

    <p>It prolongs the drug's presence in the bloodstream.</p> Signup and view all the answers

    How does reversible binding impact drug availability?

    <p>It decreases the fraction of free drug available to exert therapeutic effects.</p> Signup and view all the answers

    What property of drug binding to tissue proteins can influence its therapeutic outcomes?

    <p>Reversible binding allows for sustained drug release.</p> Signup and view all the answers

    Study Notes

    Drug Absorption Overview

    • Absorption rate and extent influenced by the environment of absorption, drug's chemical characteristics, and route of administration.
    • Route of administration significantly affects bioavailability, which is the proportion of a drug that enters systemic circulation unchanged.

    Mechanisms of Drug Absorption from the GI Tract

    • Passive Diffusion: Drugs move from areas of high concentration to low concentration without energy expenditure.
    • First-Pass Hepatic Metabolism: Rapid metabolism in the liver or gut wall reduces the amount of unchanged drug that reaches systemic circulation.

    Key Factors Affecting Drug Absorption

    • Blood Flow: Variability in blood flow to various tissues impacts drug absorption and distribution.
    • Capillary Permeability: Determined by capillary structure and the chemical nature of the drug, affects the movement of drugs into tissues.

    Drug Binding

    • Binding to Plasma and Tissue Proteins:
      • Reversible binding of drugs to plasma proteins results in a non-diffusible form, delaying transfer from vascular compartments.
      • High protein binding limits the free drug available for action and alters distribution.

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    Description

    Explore the key factors affecting drug absorption in this quiz. Understand how the environment, chemical properties, and administration routes impact bioavailability. Test your knowledge on these critical pharmacological concepts.

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