Pharmacokinetics Quiz: Drug Absorption and Factors
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Questions and Answers

What is the process of the body chemically changing a drug into a form that can be excreted?

  • Prodrug activation
  • Drug metabolism (correct)
  • Cytochrome P450 system
  • Pharmacodynamics

What type of compound is metabolized in the body to produce a drug, and is used to improve drug delivery, decrease toxicity, or target specific cells or tissues?

  • Prodrug (correct)
  • Cytochrome P450 compound
  • Half-life compound
  • Steady state compound

What is the period of time required for the concentration or amount of a drug in the body to be reduced by one-half?

  • Trough time
  • Steady state time
  • Half-life (t½) (correct)
  • Peak time

What is defined as the amount of drug administered being equal to the amount of drug eliminated?

<p>Steady state (C)</p> Signup and view all the answers

Which term refers to the time it takes for a drug to reach minimum effective concentration?

<p>Onset time (C)</p> Signup and view all the answers

What is the highest concentration of a drug in the blood called?

<p>Peak concentration (B)</p> Signup and view all the answers

Which term refers to the length of time taken for a drug to exert a therapeutic effect?

<p>Duration of action (A)</p> Signup and view all the answers

What do you call the highest concentration of a drug in the blood during therapeutic monitoring?

<p>Peak drug level (A)</p> Signup and view all the answers

Which drugs bind to receptors, activate them, and produce a desired response?

<p>'Agonists' (B)</p> Signup and view all the answers

'Nonspecific drugs' affect multiple ____________ sites.

<p>'Receptor' (D)</p> Signup and view all the answers

Epinephrine affects three different receptors: alpha1, beta1, and beta2. These are examples of ________ receptors.

<p>Selective (D)</p> Signup and view all the answers

Which type of drug interaction is characterized by one drug reducing or blocking the effect of another drug?

<p>Antagonistic interaction (A)</p> Signup and view all the answers

What is the process that involves drug movement from the gastrointestinal (GI) tract to the liver?

<p>First pass effect (C)</p> Signup and view all the answers

Which factor can influence drug distribution in the body?

<p>Blood flow (D)</p> Signup and view all the answers

What is the process of drug crossing the blood-brain barrier known as?

<p>Vascular permeability (D)</p> Signup and view all the answers

Which term refers to the ability of a drug to bind to tissue and plasma proteins?

<p>Drugs lipid solubility (A)</p> Signup and view all the answers

What factors can affect drug absorption?

<p>Fasting and food texture (D)</p> Signup and view all the answers

Which process involves the initial metabolism of a drug as it travels from the gastrointestinal tract to the liver?

<p>First pass effect (B)</p> Signup and view all the answers

What method of absorption involves the movement of substances across cell membranes without the use of energy?

<p>Passive transport (B)</p> Signup and view all the answers

What can influence drug distribution in the body?

<p>Tissue perfusion and ability of drug to bind tissue and plasma proteins (C)</p> Signup and view all the answers

Which factor can affect drug absorption?

<p>Food texture and fat content (B)</p> Signup and view all the answers

What influences drug movement across the blood-brain barrier?

<p>Vascular permeability and permeability of cell membranes (C)</p> Signup and view all the answers

What is the term for a drug's ability to bind to tissue and plasma proteins?

<p>Drugs lipid solubility (A)</p> Signup and view all the answers

How can factors like fasting and food texture affect drug absorption?

<p>By impacting disintegration and dissolution processes (A)</p> Signup and view all the answers

Flashcards

Drug Metabolism

The body's chemical transformation of drugs to make them excretory.

Metabolites

Compounds created from drugs to improve delivery or target specific cells to reduce toxicity

Half-life

Time it takes for drug concentration to drop 50%.

Steady State

Drug in and out are equal; concentration plateaus

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Minimum Effective Concentration

Drug level needed for action.

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Peak Concentration

Highest drug level in bloodstream.

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Therapeutic Effect Duration

Time a drug takes to show effect.

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Trough Concentration

Lowest drug level while monitoring.

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Agonist

Drug binding to receptor for action

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Nonspecific Drug

Drug interacting with multiple receptor sites.

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Epinephrine Receptor Types

Alpha1, Beta1, Beta2 receptors.

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Antagonistic Interaction

One drug counteracts another's effect.

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First-pass metabolism

Drug movement from GI tract to liver.

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Drug Distribution

How a drug spreads through the body.

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Blood-Brain Barrier

Specific barrier for drug permeability to the brain.

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Drug Protein Binding

Attachment of drug to tissue and plasma proteins.

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Drug Absorption Factors

Drug form, GI pH, food, and gut motility.

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Passive Diffusion

Absorption without energy.

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Drug Distribution Influences

Solubility, blood flow, and tissue protein affinity.

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Fasting/Food Impact on Absorption

Fasting and food affect drug absorption rate and extent.

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Study Notes

Drug Metabolism and Excretion

  • The body chemically transforms drugs into forms suitable for excretion, a process known as metabolism.
  • Metabolites are compounds created from drugs to enhance delivery, reduce toxicity, or target specific cells/tissues.

Pharmacokinetics Concepts

  • Half-life is the duration required for the drug concentration to decrease by 50%.
  • Steady state occurs when the amount of drug administered equals the amount eliminated.
  • Time to reach minimum effective concentration reflects dosage timing for therapeutic effectiveness.
  • Peak concentration denotes the highest level of a drug in the bloodstream.

Drug Action and Interaction

  • Therapeutic effect duration indicates how long a drug takes to show its intended benefits.
  • Trough concentration refers to the lowest level of the drug during monitoring.
  • Agonists bind to receptors and activate them to elicit a desired response.

Specificity in Pharmacology

  • Nonspecific drugs interact with multiple receptor sites, impacting various systems.
  • Epinephrine interacts with alpha1, beta1, and beta2 receptors, illustrating example receptor types.

Drug Interaction Types

  • Antagonistic interactions occur when one drug diminishes the effect of another.

Absorption and Distribution

  • The process of drug movement from the gastrointestinal tract to the liver is called first-pass metabolism.
  • Drug distribution can be influenced by factors including blood flow, binding to plasma proteins, and tissue storage.
  • Crossing the blood-brain barrier involves specific mechanisms for drug permeability.

Drug Protein Binding

  • Protein binding describes a drug's ability to attach to tissue and plasma proteins, affecting its distribution and efficacy.
  • Factors influencing drug absorption include form of the drug, gastrointestinal pH, presence of food, and gut motility.
  • Passive diffusion is a method of absorption that occurs without energy to transport substances across membranes.

Influences on Drug Dynamics

  • Drug distribution is affected by solubility, blood flow, and affinity for tissue proteins.
  • Fasting and food texture can impact the rate and extent of drug absorption due to variations in gastric emptying and enzyme activity.

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Description

Test your knowledge of drug absorption and factors affecting it with this pharmacokinetics quiz. Explore concepts such as disintegration, dissolution, passive transport, diffusion, facilitated diffusion, active transport, and factors influencing absorption.

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