Pharmacology /DENH 620 Pharmacology: Chapter 2 Drug Action And Handling
DENH 620 Pharmacology: Chapter 2 Drug Action And Handling
This deck covers key concepts from Chapter 2 of DENH 620 Pharmacology, focusing on drug action and handling. It includes definitions, processes, and mechanisms related to pharmacology.
What is a drug?
A biologically active substance that can modify cellular function
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Key Terms
Term
Definition
What is a drug?
A biologically active substance that can modify cellular function
What is the potency of a drug?
The amount of drug required to produce an effect
Efficacy
The maximum intensity/effect/response that can be produced by a drug regardless of dose. More drug will not increase efficacy but can result in an adv...
Dose response curve
Where the dose of a drug is plotted against the intensity of the effect, a curve will result
Therapeutic Index
Is a ratio of the median lethal dose (LD50) to the median effective dose (ED50). TI = LD50 / ED50
What is a receptors function?
What the drug binds to at the cell membrane to exert its effects
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Term | Definition |
---|---|
What is a drug? | A biologically active substance that can modify cellular function |
What is the potency of a drug? | The amount of drug required to produce an effect |
Efficacy | The maximum intensity/effect/response that can be produced by a drug regardless of dose. More drug will not increase efficacy but can result in an adverse reaction |
Dose response curve | Where the dose of a drug is plotted against the intensity of the effect, a curve will result |
Therapeutic Index | Is a ratio of the median lethal dose (LD50) to the median effective dose (ED50). TI = LD50 / ED50 |
What is a receptors function? | What the drug binds to at the cell membrane to exert its effects |
Agonist | Is a drug that has affinity for a receptor, binds to the receptor, and produces an effect |
Antagonist | Counteracts the action of the agonist. Three types: competitive, non-competitive, physiologic |
Pharmacokinetics | The study of how a drug enters the body, circulates within the body, is changed by the body, and leaves the body |
What are the four major steps that influence the movement of a drug? | Absorption, Distribution, Metabolism, Excretion |
Simple diffusion | Where lipid soluble substances move across the lipoprotein membrane by passive transfer |
Active Transport | A process by which a substance is transported against a concentration gradient mediated by transport carriers |
Facilitated diffusion | Does not move against a concentration gradient, transport via carriers |
Absorption | Where drug molecules are transferred from the site of administration to the circulating blood |
What factors influence the rate of absorption of a drug? | The physicochemical factors, the site of absorption, the drug's solubility |
Un-Ionized means? | The uncharged portion of weak electrolytes readily crosses bodily membranes more readily because it is lipid soluble |
Ionized | Weak electrolytes will pass across membranes with more difficulty because it is less lipid soluble |
In the presence of infection, the acidity of the tissue ___ and the pH ___ and the effect of local anesthetics ___? | Increases, Decreases, Decreases |
What are the different types of absorption? | Ionization, Oral, Injection Site |
Drugs that are least soluble with have the _____? | Longest duration of action |
Distribution | The passage of drugs into various body compartments such as plasma, interstitial fluids, and intracellular fluids |
Redistribution | The movement of a drug from the site of action to nonspecific sites of action |
Metabolism | (aka Biotransformation) the body’s way of changing a drug so that it can be more readily excreted by the kidneys |
What is the first pass effect? | When drugs that are given orally and pass through the liver prior to being circulated in systemic circulation |
Excretion | Where drugs can be excreted by the kidneys, lungs, bile, GI Tract, sweat, saliva and breast milk. Renal (Kidneys is the most important) |
Half life | Is the amount of time that passes for a drug's concentration to fall to half of its original blood level |
Kinetics | Is a mathematical representation of the way drugs are removed by the body |
Route of Administration | Is the way a drug is administered which affects the onset and duration of response |
Duration | The length of a drug's effect |
Enteral Route | Drugs that are placed directly in the GI Tract by oral or rectal administration |
Parenteral Route | Bypasses the GI Tract and includes various injection routes, inhalation and topical administration |
Oral Route | The most common and most popular route of administration in the US |
Topical Route | Application to body surfaces or sublingually (under tongue) |