Lecture 1 - Intro Flashcards

1
Q

Potential for drug-receptor binding.

A

Affinity

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2
Q

Binding site w/ biological effect.

A

Receptor

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3
Q

Capacity to produce a biological effect.

A

Intrinsic activity

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4
Q

Having intrinsic activity and affinity.

A

Agonist

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5
Q

Affinity without intrinsic activity.

A

Antagonist

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6
Q

A stereospecific phenomenon whereby a bound ligand influences specificity of a second site

A

Allostery

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7
Q

Efficacy

A

[affinity] x [intrinsic activity]

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8
Q

‘effective’ concentration in 50% of subjects

A

EC50

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9
Q

‘effective’ dose in 50% of subjects

A

ED50

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10
Q

‘inhibitory’ concentration in 50% of subjects

A

IC50

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11
Q

Result in chronic antagonism.

A

hypersensitivity

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12
Q

minimum amount of drug producing maximum therapeutic effect

A

maximum dose

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13
Q

Low intrinsic activity with potency and affinity within therapeutic range.

A

partial agonist

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14
Q

Drug –> Body

A

Pharmacodynamics

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15
Q

Body –> Drug (ADME)

A

Pharmacokinetics

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16
Q

Drug –> Disease

A

Pharmacotherapeutics

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17
Q

Science of drug dosing

A

Posology

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18
Q

response to a give dose

A

Potency

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19
Q

Loss of pharmacological effect.

A

Resistance

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20
Q

Ability to produce a desired effect versus adverse effect.

A

Selectivity

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21
Q

Ability to act at a specific receptor.

A

Specificity

22
Q

Rapidly decreasing therapeutic response.

A

Tachyphylaxis

23
Q

congenital malformation

A

Teratogenesis

24
Q

Amount of active drug reaching target tissue.

A

Bioavailability

25
Q

LD50:ED50 or TD50:ED50

A

therapeutic index

26
Q

Diagnostic pharmaceutical agent

A

DPA

27
Q

Therapeutic pharmaceutical agent

A

TPA

28
Q

insulin

A

Supplemental drug type

29
Q

glucose

A

Supportive drug type

30
Q

low dose aspirin

A

Prophylactic drug type

31
Q

fluorescein

A

Diagnostic drug type

32
Q

Methotrexate

A

Therapeutic drug type

33
Q

Tear film

A

~10ul

34
Q

max surface area

A

~30 ul

35
Q

gt?

A

25-56 ul

36
Q

Basal tear flow

A

0.5-2.2 ul/min

37
Q

cornea in diabetes

A

thick

38
Q

cornea in keratoconus

A

thin

39
Q

Concentration independent; rate limiting barrier or saturable carrier; constant amount of clearance; elimination per unit time is linear

A

Zero order

40
Q

Concentration dependent; non-saturable carrier; constant proportion of clearance & constant half-life; elimination per unit time is exponential

A

1st order (most drugs)

41
Q

saturable carrier at high concentrations only

A

mixed-order

42
Q

High abuse, no known medical use, lack of safety

A

Schedule 1 Drug; unavailable like heroin

43
Q

High abuse, some medical use, high risk of dependency

A

Schedule 2 Drug; morphine

44
Q

Lower abuse, medical use, moderate dependency risk

A

Schedule 3 Drug; valium

45
Q

Limited abuse, high medical use, limited dependency risk

A

Schedule 4 Drug; codeine

46
Q

Minor problems, may be available w/o Rx

A

Schedule 5 Drug; penicillin

47
Q

No evidence of risk in women.

A

A

48
Q

No evidence of risk in animals.

A

B

49
Q

Animal toxicity evidence

A

C

50
Q

Risk may equal benefits

A

D

51
Q

Risk > benefits

A

X

52
Q

Off-label drug use

A

Practice of prescribing a drug for a non-FDA approved indication