Routes of Drug Administration
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Questions and Answers

Drugs are classified based on their pharmacotherapeutic actions, pharmacological actions, molecular actions, and chemical nature.

True (A)

Receptors are only located in cell membranes and do not interact with intracellular ligands.

False (B)

Agonists are ligands that bind but do not activate receptors.

False (B)

There are five main types of receptors that include receptors directly linked to ion channels.

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

Most drugs produce their effects by interacting with specific protein receptors.

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

Receptors are classified as agonists or antagonists depending on their interaction with drugs.

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

Potency refers to the volume of a drug needed to elicit a response.

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

Pharmacodynamics deals with the absorption, distribution, metabolism, and excretion of drugs in the body.

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

Topical application of drugs offers advantages such as higher concentration in the target tissue and fewer side effects.

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

Pharmacology is the study of the actions, mechanisms, uses, and adverse effects of drugs.

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

All drugs can be divided into two groups: medicinal drugs and nonmedicinal (social) drugs.

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

Cannabis, heroin, and cocaine are examples of medicinal drugs.

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

Nicotine and alcohol are considered nonmedicinal (social) drugs.

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

Enteral administration is the most predictable way of drug administration due to potential metabolism in the liver and gastrointestinal tract.

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

Rectal administration is consistent and reliable for drug delivery.

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

Sublingual and buccal administration can be used to avoid first-pass metabolism for drugs with a disagreeable taste.

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

Parenteral administration involves the administration of drugs through the gut.

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

Insulin, a protein drug, can be administered orally due to its stability in the gastrointestinal tract.

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

Intravenous injection allows for slow drug distribution in small volumes.

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

Enteral administration is the most predictable route for drug administration.

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

Parenteral administration is important for drugs that do not require continuous infusion.

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

Rectal administration bypasses the liver metabolism and gastrointestinal tract.

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

Parenteral administration is the most direct route for drug delivery.

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

Parenteral administration can be used for drugs that cannot be administered orally due to stability, inactivation, or uncertain absorption.

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

Parenteral administration is important for drugs that damage tissues.

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

Parenteral routes of administration include subcutaneous, intramuscular, epidural, and intrathecal injections, as well as transdermal patches.

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

Transdermal patches are the most direct way of drug administration, allowing the drug to enter the bloodstream directly and bypass absorption barriers.

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

Bioavailability considers both absorption and metabolism and describes the proportion of the drug that enters the systemic circulation.

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

Bioavailability is always 100% after oral administration.

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

Drug absorption is affected by physiochemical and physiological factors.

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

Cell membranes are composed of lipid bilayers, and absorption is usually proportional to the lipid solubility of the drug.

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

Small molecular size favors drug absorption.

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

Most drugs are able to diffuse across membranes in their uncharged state.

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

The pH of the environment and the pKa value of the drug are not important in determining the fraction in the unionized form that is able to diffuse across cell membranes.

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

The pH of the environment is important for drug absorption, especially for weak bases, weak acids, or amphoteric drugs.

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

Most drugs are not affected by the physiochemical and physiological factors in their absorption process.

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

Drug absorption will be 100% after intravenous injection and will not depend on the physiochemical characterizations of the drug or the individual.

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

Flashcards

Drug Classification

Categorization of drugs based on their effects, actions, chemical makeup, and other factors.

Receptors and Ligands

Receptors are proteins that bind to ligands (like drugs) to trigger a response; ligands can affect intracellular or extracellular receptors.

Agonist

A ligand that binds to and activates receptors, causing a biological response.

Types of Receptors

Receptors can be linked to ion channels, or have other mechanisms of action.

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Drug-Receptor Interaction

Most drug effects are produced by interacting with specific protein receptors on the cell surface or inside the cell.

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Agonist vs. Antagonist

Receptors are categorized as agonists (activators) or antagonists (blockers) based on their interaction with drugs.

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Potency

The amount of a drug needed to produce a specific effect.

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Pharmacodynamics

The study of how drugs interact with the body to produce their effects.

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Topical Application

Drug application directly to the site of action, often for localized effects.

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Pharmacology

The study of drugs, including their actions, mechanisms, uses, and side effects.

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Medicinal vs. Nonmedicinal Drugs

Medicinal are used for healing, social (nonmedicinal) for recreation or other purposes.

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Enteral Administration

Drug administration through the digestive system(oral, rectal, etc.)

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Parenteral Administration

Drug administration by routes other than the digestive system (e.g., injection).

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First-Pass Metabolism

The breakdown of a drug as it passes through the liver or gastrointestinal tract; reduces bioavailability.

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Bioavailability

The proportion of an administered dose of a drug that reaches the systemic circulation.

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Drug Absorption

The process by which a drug enters the bloodstream.

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Lipid Solubility

A factor influencing drug absorption; more lipid-soluble drugs pass membranes more easily.

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Molecular Size

Smaller molecules generally absorb more easily.

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Uncharged State of Drugs

Drugs in uncharged form can more easily pass through cell membranes.

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pKa and pH

The pH of the environment and the pKa of the drug affect its ability to cross membranes.

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Intravenous Injection

Direct injection into a vein, resulting in immediate and predictable effects.

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Transdermal Patches

Drug delivery through the skin, bypassing gut, metabolizing, and absorption barriers.

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Study Notes

  • Enteral administration is the least predictable way of drug administration due to potential metabolism in the liver and gastrointestinal tract.
  • Drugs must cross several barriers, and some may not be suitable for oral administration due to their physicochemical properties.
  • Sublingual and buccal administration can be used to avoid first-pass metabolism and is useful for drugs with a nondisagreeable taste or for drugs that are unstable or inactivated in the gastrointestinal tract.
  • Rectal administration, such as suppositories, also reduces first-pass metabolism but is inconsistent.
  • Parenteral administration is the administration of drugs in a manner that avoids the gut.
  • Insulin, a protein drug, is destroyed by the stomach acidity and digestive enzymes and must be injected subcutaneously instead.
  • Intravenous injection is a direct route of administration that bypasses absorption barriers and allows for rapid drug distribution in large volumes.
  • Parenteral administration is important for drugs that must be given continuously by infusion or for drugs that damage tissues.
  • Enteral administration is the least predictable route due to potential metabolism in the liver and gastrointestinal tract, but it can be used for certain drugs when appropriate.
  • Parenteral administration is the most direct route, allowing drugs to enter the bloodstream directly, bypass absorption barriers, and act rapidly.
  • Parenteral administration can be used for drugs that cannot be administered orally due to stability, inactivation, or uncertain absorption.
  • Parenteral administration is important for drugs that require continuous infusion or for drugs that damage tissues.

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Description

Test your knowledge of different routes of drug administration with this quiz. Learn about the advantages and disadvantages of topical medication, inhaled medication, and enteral medication.

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