Intro to pharmacokinetics Part 2 Flashcards

1
Q

What varies overtime in first order kinetic modelling ?

A

The rate of elimination

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2
Q

What can be said about the half life in first order kinetic modelling ?

A

It stays constant

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3
Q

Which pharmacokinetic model is less accurate and why?

A

1st compartment model

Assumption that the human being is one big puddle of water and is a less accurate model when it comes to time

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4
Q

What is the two-compartment model?

A

There is a tissue compartment and a central compartment and is a more accurate model

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5
Q

Why is half life important ?

A

It allows you to calculate the clearance as the clearance is inversely proportional to the drug

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6
Q

How do you calculate clearance ?

A

Volume of plasma cleared of drug / unit time

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7
Q

The bigger the clearance the ________ the half life

A

Smaller

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8
Q

After 5 half lives, how much of the drug have you eliminated ?

A

96.9% - essentially eliminated

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9
Q

What varies in zero order pharmacokinetics ?

A

Half life (opposite of first order)

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10
Q

What causes zero order pharmacokinetics (RARE)?

A

When the elimination action pathways are saturated e.g. alcohol can cause this

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11
Q

Why would a patient suffer from side effects longer due to a zero order pharmacokinetics drug?

A

As the half life is longer

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12
Q

What is steady state ?

A

the rate of infusion = the rate of elimination

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13
Q

What is the therapeutic window ?

A

The space between the minimum effective concentration and the minimum toxic concentration

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14
Q

If you wanted to get the drug into the therapeutic window quickly, what would you do?

A

Use an IV or a double dose

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15
Q

How do you calculate dose rate?

A

Drug concentration x clearance

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16
Q

How do you calculate volume of distribution?

A

Dose / drug concentration

17
Q

How do you calculate maintenance dose?

A

Dosing rate x dosing interval / bioavailability