1S Flashcards

1
Q

T or F:

The protonated form of a weak acid is more lipid soluble

A

True

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2
Q

T or F:

Partial agonist does not evoke as great a response as that of the full agonist.

A

True

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3
Q

Rate of diffusion:

  1. alveolar membrane 2. small intestines
A

1>2

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4
Q

T or F:

Weak basic drugs are excreted faster in acidic urine.

A

True

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5
Q

Increase in A will ?

A. surface area B. rate of diffusion.

A

increase in B

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6
Q

T or F:

All chemicals are toxic in some individual at some dose.

A

True

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7
Q

This was the precursor of Pharmacology:

A

Materia Medica

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8
Q

T or F:

Plant chemicals are different from industrial chemical manufactured drugs.

A

False

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9
Q

Chemicals which generally have harmful effects:

A

Poison

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10
Q

Chemicals which are not synthesized in the body:

A

Xenobiotics

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11
Q

T or F:

Facilitated diffusion employs special carrier molecules to transport the drug molecule against a concentration gradient.

A

False

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12
Q

T or F:

Quaternary amines are permanently charged thus are always water soluble.

A

True

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13
Q

Transport of Iron bound to transferrin

A

Endocytosis / Exocytosis

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14
Q

van der Waals forces are considered as:

A

Electrostatic

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15
Q

Pharmacologic Response:

  1. Agonist + Allosteric activator
  2. Agonist + Allosteric inhibitor
A

1>2

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16
Q

Drug excretion

A

Pharmacokinetics

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17
Q

Drug metabolism

A

Pharmacokinetics

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18
Q

Drug body-interaction

A

Pharmacokinetics & Pharmacodynamics

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19
Q

Chemicals that binds to a different site and decreases the agonist effect

A

Allosteric inhibitor

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20
Q

T or F:

Partial agonist evokes a great response as that of the full agonist

A

False

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21
Q

Rate of diffusion:

  1. small intestines 2. stomach
A

1>2

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22
Q

Substances that act on biologic systems at the chemical (molecular) level and alter their functions

A

Drug

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23
Q

Important in the choice of administration of a particular drug for a particular patient

A

Pharmacokinetics

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24
Q

T or F:

Drug molecules that are bound to plasma proteins can permeate aqueous pores

A

False

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25
Q

increase in a will?

A. pH of the medium
B. renal reabsorption of a weak base

A

increase in B

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26
Q

T or F:

High molecular weight drug have difficulty in diffusing from one compartment to
another.

A

True

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27
Q

Chemicals that binds to a different site and increases the agonist affinity

A

Allosteric activator

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28
Q

Interaction of drugs with the internal walls of receptor pockets

A

hydrophobic

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29
Q

Pharmacologic Response:

  1. Partial agonist
  2. Full agonist
A

1<2

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30
Q

T or F:

Quaternary amines are permanently charged thus are always lipid soluble.

31
Q

T or F:

The unprotonated form of a weak acid is more lipid soluble.

32
Q

Denotes the actions of the drug on the body

A

pharmacodynamics

33
Q

Describes the effects of the body on drugs

A

Pharmacokinetics

34
Q

Drug absorption

A

pharmacokinetics

35
Q

T or F:

Drug molecules that are bound to plasma proteins can not permeate aqueous pores.

36
Q

strong bond between permanently charged molecules.

A

electrostatic

37
Q

T or F:

Allosteric inhibition is not overcomed by increasing the dose of agonist.

38
Q

T or F:

Inert binding sites does not affect drug distribution

39
Q

Body of knowledge concerned with the action of chemicals on biologic systems.

A

Pharmacology

40
Q

Rate of diffusion:

  1. skin
  2. small intestines
41
Q

Pharmacologic Response:

  1. Agonist + Allosteric inhibitor
  2. Agonist + Allosteric activator
42
Q

Drug Distribution

A

Pharmacokinetics

43
Q

Plays the major role in deciding whether that drug is appropriate therapy for a particular symptom or disease

A

Pharmacodynamics

44
Q

T or F:

The protonated form of a weak acid is more water soluble

45
Q

T or F:

The unprotonated form of a weak acid is more water soluble.

46
Q

These are receptors with no discovered ligands

A

Orphan receptors

47
Q

Chemicals that bind to a different site and increases agonist effect

A

Allosteric activator

48
Q

Based on Fick’s law the flux would be inversely proportional to:

49
Q

Rate of diffusion:

  1. Alveolar membrane
  2. Stomach
50
Q

T or F:

Allosteric inhibition is can be overcomed by increasing the dose of agonist.

51
Q

Pharmacologic Repsonse:

  1. Agonist + allosteric activator
  2. Agonist +allosteric inhibitor
52
Q

Drug receptor binding which is not readily broken.

53
Q

Increase in A will?

A. thickness of membrane
B. rate of diffusion

A

decrease in B

54
Q

T or F:

Weak basic drugs are excreted faster in acidic urine

55
Q

T or F:

Facilitated diffusion employs special carrier molecules to transport the drug molecule down their concentration gradient.

56
Q

T or F:

Transport of drugs that use special carriers can be saturated and inhibited

57
Q

Substances that act on biologic systems at the chemical (molecular) level and alter their functions.

58
Q

Important in the choice of administration of a particular drug for a particular patient:

A

Pharmacokinetics

59
Q

T or F:

All substances can be toxic under certain conditions

60
Q

Concerned with toxic effects.

A

Pharmacodynamics

61
Q

Plays the major role in deciding whether that drug is appropriate therapy for a particular symptom or disease.

A

Pharmacodynamics

62
Q

Determines the group in which the drug is classified.

A

Pharmacodynamics

63
Q

T or F:

Weak acid drugs are excreted faster in alkaline urine

64
Q

Facilitated diffusion is classified as

A

special carriers

65
Q

T or F:

There should be artificial separation between scientific therapies and alternative complementary medicine.

66
Q

Which of the following is the weakest electrostatic bond

A

van der waals force

67
Q

Chemicals with exclusive harmful effects derived from biologic origin:

68
Q

Rate of diffusion:

  1. alveolar membrane
  2. Stomach:
69
Q

T or F:

The protonated form of a weak base is more lipid soluble.

70
Q

T or F:

Weak basic drugs are excreted faster in alkaline urine

71
Q

Secretion of neurotransmitter

A

endocytosis/exocytosis

72
Q

Area of pharmacology concerned with the undesirable effects of chemicals on biologic systems

A

toxicology

73
Q

Hydrogen bonds between the drug and its receptor are

A

electrostatic

74
Q

increase in A will?

A. concentration difference B. rate of diffusion

A

increase in B