Basic Principles of Pharmacology Flashcards

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
Q

What is meant by potency

A

The amount of drug that is necessary to achieve a certain effect

26
Q

What is the efficacy

A

This is the maximum possible effect of the drug

27
Q

What is an agonist

A

This is a drug that binds to and activates that receptor

28
Q

What is an antagonist

A

This a molecule that binds to a receptor and in doing so prevents other molecules from binding

29
Q

What is the difference between a full and a partial agonist

A

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
Q

What are the 4 main types of antagonists

A
  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
Q

What is meant by tolerance

A

This is where larger doses are needed to experience the same effects

32
Q

What are the 3 main mechanisms of tolerance

A
  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