Chapter 4 Flashcards

1
Q

bioavailability

A

percent of drug administered that enters the systemic circulation

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2
Q

pinocytosis/phagocytosis

A

type of cellular movement that allows intake of large molecules

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3
Q

volume of distribution

A

indicator of how well a drug is distributed throughout the body

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4
Q

what type of molecule can perform passive diffusion

A

lipophilic, nonionized, small

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5
Q

primary site of drug metabolism

A

liver

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6
Q

drug distribution

A

physiological movement of drugs from the systemic circulation to the tissues

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7
Q

induce

A

describes an increase in the rate of metabolism by an enzyme system

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8
Q

ionized

A

charged

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9
Q

passive diffusion movement

A

high concentration to low concentration

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10
Q

active transport movement

A

low concentration to high concentration

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11
Q

what types of drugs absorb well in the GI tract?

A

hydrophilic drugs

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12
Q

which body compartment gets adequate drug levels the fastest?

A

fat

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13
Q

what condition will allow for greater volume of distribution?

A

normal conditions
dehydrated animals will have less

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14
Q

drug affinity

A

measure of a drug’s strength at which it binds to its receptor

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15
Q

bioequivalency

A

when two drugs would be expected to be essentially the same

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16
Q

first-pass metabolism

A

phenomenon of drug metabolism in which the concentration of active drug is greatly reduced before it reaches systemic circulation because it passes through liver first

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17
Q

acidic drug in an acidic environment

A

nonionized molecules

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18
Q

acidic drug in alkaline environment

A

ionized molecules

19
Q

alkaline drug in acidic environment

A

ionized molecules

20
Q

alkaline drug in alkaline environment

A

nonionized molecules

21
Q

ion trapping

A

occurs when a drug molecules changes from ionized to nonionized form as it moves from one body compartment to another

22
Q

tissue perfusion

A

relative amount of blood supply to an area or body system

23
Q

free drug

A

drug that isn’t bound to a protein and is free in blood
penetrates tissues

24
Q

increased protein binding

A

less free drug

25
decreased protein binding
more free drug
26
more free drug causes more chance for ______
toxicity
27
biotransformation
(drug metabolism) chemical alteration of drug molecules into metabolites by body cells
28
characteristics of metabolites
more hydrophilic, eliminated in urine or bile, wider distribution to tissues or excretion
29
reactions that cause drugs to be altered by metabolism
1. oxidation reactions (lose electrons) 2. reduction reactions (gain electrons) 3. hydrolysis (adding H2O causing split) 4. conjugation (addition of substance which makes drug more water soluble)
30
other sites that can absorb drugs
kidneys, small intestine, brain/neurologic tissue, lungs, skin
31
altered absorption
one drug alters absorption of other drugs (antacids)
32
altered metabolism
same enzyme needed to metabolize more than one drug, slows down metabolizing of both drugs
33
altered elimination
some drugs act directly on kidney and decrease elimination of other drugs (diuretics)
34
microsomal enzyme inducers
drugs that induce enzyme system alter metabolism by causing liver to become more efficient
35
drug tolerance
increased metabolism due to enzyme induction metabolic: drug is metabolized more rapidly with chronic use cellular: decreased cellular receptors with repeated use
36
pathways for elimination
kidneys, liver, intestine, lungs, milk
37
half life
time required for the concentration of drug in the blood to be reduced by half
38
steady-state concentration
drug concentration reaches a plateau where peak concentrations and lowest concentrations are the same after repeated doses of drug
39
minimal effective concentration (MEC)
onset of action begins when drug achieves MEC
40
peak plasma level
elimination rate of drug is equivalent to rate of absorption
41
time to peak
time of administration to the time that the peak plasma level is reached
42
minimum toxic concentration (MTC)
plasma level at which toxic effects are observed
43
loading dose
given to rapidly achieve therapeutic plasma levels
44
dissociation constant K
measure of a drug's affinity for its receptor