Ch 2 - Pharmacokinetics and Pharmacodynamics Flashcards

1
Q

Movement of drug through the body and how the body affects the drug

A

Pharmacokinetics

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2
Q

How the drug affects the body; how the drug initiates its therapeutic or toxic effect at the cellular or systemic level

A

Pharmacodynamics

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3
Q

Drug administration, absorption, distribution, and elimination

A

Pharmacokinetics

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4
Q

Range of drug concentration in the blood that yields a sufficient therapeutic response without toxic reactions. Varies between individuals.

A

Therapeutic Window

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5
Q

Following administration by oral, sublingual or rectal routes

A

Enteral absorption

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6
Q

Following administration by inhalation, IV, IM, Subq, topical or transdermal route

A

Parenteral absorption

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7
Q

Fraction of drug that reaches systemic circulation.

IV drugs = 100%

A

Bioavailability

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8
Q

Presence or absence of food in stomach
Blood flow to area or absorption
Dosage form of drug
GI motility

A

Factors affecting Absorption

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9
Q

Molecules move from one side of a barrier to another without expending energy

A

Passive diffusion

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10
Q

Membrane proteins act as carrier molecules to transport substances across all membranes

A

Active transport

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11
Q

Blood flow to an area
Lipid or water solubility
Protein binding
Obesity (lipid soluble drugs)

A

Factors affecting Distribution

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12
Q

Drug is available to exert its effect

A

Free/Unbound Drug

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13
Q

Drug is inactive; cannot leave bloodstream

A

Protein Bound Drug

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14
Q

Theoretical parameter calculated by determining amount of drug in the body (dose administered) divided by the concentration of drug in the plasma

A

Apparent Volume of Distribution

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15
Q

Metabolism and Excretion

A

Methods of Elimination

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16
Q

Liver, kidneys, GI tract

A

Sites of Metabolism

17
Q

Kidneys, lower GI tract, lungs, skin

A

Sites of Excretion

18
Q

Change to water soluble form by enzymes

A

Biotransformation

19
Q

Drug may be excreted in bile and then reabsorbed in lower GI tract

A

Enterohepatic Recirculation

20
Q

Time required for half of drug to be eliminated

21
Q

Equilibrium between rates of absorption and elimination

A

Steady state

22
Q

Removal of drug from plasma or organ

23
Q

Rate of elimination is constant but amount of drug eliminated is proportional to concentration

A

First-order kinetics

24
Q

Fixed amount of drug eliminated, independent of concentration

A

Zero-order kinetics

25
Route that provides large surface area for absorption and quick entry into bloodstream. Bypasses first-pass effect allowing for high bioavailability
Inhalation of Medications
26
Route of administration that allows continuously delivered medication to achieve a constant blood level
Transdermal
27
Component of cell or enzyme to which an endogenous substance binds or attaches to initiate a chain of biochemical events
Drug Receptor
28
Any chemical that interacts with a receptor
Ligand
29
Open or close channels to allow certain ions to pass through cell membrane
Gated ion channels
30
Has its ligand-binding domain on the cell's surface
Transmembranous receptors
31
Generate intracellular second-messengers
G protein-coupled receptors
32
Drugs attach to these receptors and initiate direct changes in the cell by affecting DNA transcription
Intracellular receptors
33
These drugs can traverse the lipid bilayer and enter the cell
Lipid soluble
34
Degree to which a drug is attracted to a receptor
Affinity
35
Drugs exist in two forms with mirror-image spatial arrangements called enantiomers or isomers (like right and left hands) which affect interaction with receptors
Chirality
36
Drugs that display a degree of affinity for a receptor and stimulate a respons
Agonists
37
Drugs that display an affinity for a receptor but do not elicit a response
Antagonists