Basic Principles of Pharmacology Flashcards

(32 cards)

1
Q

Define pharmacology

A

This is the study of substances that interact with living systems through chemical processes

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2
Q

What are the the 5 R of medication safety

A

Right
1. Dose
2. Time
3. Route
4. Patient
5. Drug

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3
Q

Define pharmacokinetics

A

This is the time course of the drug and its metabolites through the body

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4
Q

What are the 4 main principles of pharmacokinetics

A
  1. Absorption
  2. Distribution
  3. Metabolism
  4. Excretion
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5
Q

What is the clearance

A

This is a measure of the bodies ability to eliminate a drug

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6
Q

What is the volume of distribution

A

This is a measure of a drugs propensity to remain in the plasma or distribute into the tissue thus a drug with a high volume of distribution will leave the plasma and enter the extravascular compartment

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7
Q

What is the half life

A

This is the time taken for the body to reduce the conc. of a drug by half

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8
Q

Define the therapeutic window

A

This is the difference between the minimal toxic conc. and the maimal effective conc.

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9
Q

How long does it take to reach the steady state

A

5 half lives

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10
Q

What is a loading dose

A

A larger than maintenance dose that helps to reach the therapeutic window faster

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11
Q

Define absorption

A

This is how much of the administered drug reaches the systemic circulation

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12
Q

What is first pass metabolism

A

This is the portion of orally administered drug that is removed by the liver before it reaches the systemic circulation

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13
Q

What are P glycoprotein transporters

A

These are active transporters that efflux lipid soluable drugs that cross the cell membrane in the gut and blood tissue barriers

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14
Q

Which drugs are able to pass through the BBB

A
  1. Small lipid soluable drugs
  2. Drugs that are substrates of transporters
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15
Q

What is a prodrug

A

This is a drug that is inactive or less active as compared to its metabolite and so needs to be metabolised to exert its effect

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16
Q

What are the 2 main processes of drug metabolism

A
  1. Introduction or exposure of the functional group through a ROH rxn
  2. Polar conjugation: This is where a polar group is added to facilitate excretion
17
Q

What is meant by first order kinetics of metabolism

A

This is where a constant proportion of the drug is removed per unit time e.g. 10% and so the rate of metabolism increases with increased conc.

18
Q

What is zero order kinetics in drug metabolism

A

This is where a constant amount of drug is removed per unit time and so there is exponential increases in drug conc. as a fixed amount is removed

19
Q

What is meant by inhibition and induction

A

Inhibition: This is where a drug binds to an enzyme causing it to stop functioning thus increasing the conc. of drug in circulation as it is not removed

20
Q

What is meant by induction

A

This is where there is increased expression of the genes that regulate enzymes and so there is an increase in the conc. of the enzyme causing faster removal of a drug

21
Q

Who are the special populations in prescribing drugs

A

Liver and renal disease
Elderly and children
Pregnant and lactating
Porphyria

22
Q

Define pharmacodynamics

A

This the study of the biochemical and physiological effects of the drugs

23
Q

What is the ED50

A

This is the dose that elicits an effective response in 50% of individual

24
Q

What is the LD50

A

This is the lethal dose in 50% of individuals

25
What is meant by potency
The amount of drug that is necessary to achieve a certain effect
26
What is the efficacy
This is the maximum possible effect of the drug
27
What is an agonist
This is a drug that binds to and activates that receptor
28
What is an antagonist
This a molecule that binds to a receptor and in doing so prevents other molecules from binding
29
What is the difference between a full and a partial agonist
A full agonist is a agonist that once it occupies the reseptor it initiated the full physiological effect and a partial produces a submaximal response
30
What are the 4 main types of antagonists
1. Pharmacological antagonist: This is when the antagonist interferes directly with the receptor 2. Physiological: 2 drugs act in opposing physiological effects 3. Chemical: This is were 2 drugs in solution react with one another to neutralize one another 4. Physical: They act through physical properties, such as solubility, adsorption, or distribution, rather than molecular interactions with receptors or enzymes e.g. charcoal
31
What is meant by tolerance
This is where larger doses are needed to experience the same effects
32
What are the 3 main mechanisms of tolerance
1. Pharmacokinetic clearance: This is where there is increased clearance induced by repeated doses 2. Pharmacodynamic clearance: This is where there is a change to the number of receptors or their function due to repeated exposure to the drug 3. Behavioral tolerance: This is learned behavior that leads to diminished effects of the drugs