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

A

Half-life

21
Q

Equilibrium between rates of absorption and elimination

A

Steady state

22
Q

Removal of drug from plasma or organ

A

Clearance

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
Q

Route that provides large surface area for absorption and quick entry into bloodstream.

Bypasses first-pass effect allowing for high bioavailability

A

Inhalation of Medications

26
Q

Route of administration that allows continuously delivered medication to achieve a constant blood level

A

Transdermal

27
Q

Component of cell or enzyme to which an endogenous substance binds or attaches to initiate a chain of biochemical events

A

Drug Receptor

28
Q

Any chemical that interacts with a receptor

A

Ligand

29
Q

Open or close channels to allow certain ions to pass through cell membrane

A

Gated ion channels

30
Q

Has its ligand-binding domain on the cell’s surface

A

Transmembranous receptors

31
Q

Generate intracellular second-messengers

A

G protein-coupled receptors

32
Q

Drugs attach to these receptors and initiate direct changes in the cell by affecting DNA transcription

A

Intracellular receptors

33
Q

These drugs can traverse the lipid bilayer and enter the cell

A

Lipid soluble

34
Q

Degree to which a drug is attracted to a receptor

A

Affinity

35
Q

Drugs exist in two forms with mirror-image spatial arrangements called enantiomers or isomers (like right and left hands) which affect interaction with receptors

A

Chirality

36
Q

Drugs that display a degree of affinity for a receptor and stimulate a respons

A

Agonists

37
Q

Drugs that display an affinity for a receptor but do not elicit a response

A

Antagonists