Introduction to Pharmacology Flashcards

1
Q

Pharmacokinetics

A

what the body does to the drug; absorption, distribution, metabolism, elimination

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2
Q

Pharmacodynamics

A

what the drug does to the body

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3
Q

Therapeutic Index

A

LD 50/ED 50

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4
Q

Therapeutic Window

A

TD 50/ED 50 - minimum toxic concentration/minimum effective concentration

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5
Q

Chemical Bond Strength

A
Covalent
Ionic
Hydrogen
Hydrophobic 
van der Waals
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6
Q

Interaction Antagonism

A

1 + 1 = 0

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7
Q

Interaction Potentiation

A

1 + 0 = 3

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8
Q

Interaction Synergism

A

1 + 1 = 3

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9
Q

Interaction Addition

A

1 + 1 = 2

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10
Q

Down - Regulation

A

continued simulation with agonist results in a reduced of receptors, subsequent exposure is diminished

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11
Q

Up - Regulation

A

continued administration with antagonist results in an increased number of receptors, causes the development of tolerance

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12
Q

pKa

A

ionization constant
0 = 50/50
0.5 = 75/25
>1 = 99/1

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13
Q

Functional Tolerance

A

‘pharmacodynamics tolerance’ - change in tissue sensitivity

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14
Q

Dispositional Tolerance

A

‘pharmacokinetic tolerance’ - can in absorption, distribution, metabolism, or excretion

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15
Q

Phase 1 Metabolism

A

oxidation, reduction, hydrolysis

usually form active toxic metabolites

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16
Q

Phase 2 Metabolism

A

conjugation, synthesis

usually form inactive polar metabolites

17
Q

First Order Pharmacokinetics

A

half-life: it takes the same amount of time to reduce the concentration by 50%, no matter how much drug

18
Q

Zero-Order Elimination

A

constant amount is eliminated over time

19
Q

alpha half-life

A

redistribution half-life of the drug

20
Q

beta half-life

A

after the drug is distributed; due to metabolism

21
Q

4 categories of patients with protein deficiency

A
  • malnutrition
  • liver disease
  • kidney disease
  • 3rd trimester of pregnancy
22
Q

protein binding: acidic versus basic drugs

A
  • acidic drugs = albumin

- basic drugs = AAG

23
Q

protein binding _____ is significant

A

> 90%

24
Q

volume of distribution

A
<0.6 = low, not lipid soluble
>0.6 = high, lipid soluble