Pharmacokinetics and pharmacodynamics lectures Flashcards

1
Q

Pharmacokinetics vs pharmacodynamics?

A

Kinetics: what the body does to the drug.

Dynamics: what the drug does to the body.

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2
Q

4 stages of pharmacokinetics:

A

Absorption, distribution, metabolism, excretion.

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3
Q
A
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4
Q

What is the area under the curve dependant on?

A

Amount in systemic circulation which is dependant on the amount administered and the rate of elimination.

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5
Q
A
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6
Q

What is fracton of dose “F” mean?

How do you calculate it?

A
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7
Q

Explain ionisation of a weak base/weak acid drug?
What does this mean for absorption?

A
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8
Q

What are the main routes of clearance of a drug?

A
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9
Q

Explain volume of distribution?

Why is vd useful?

A

Volume of distribution: how well a drug is distributed through the body. The more compartments a drug gets to the higher the volume of distribution.

  • Ab=amount of drug administered, Cp=concentation of drug in plasma.
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10
Q

How do you work out the loading dose?

A
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11
Q

How can Vd and Cl be used to figure out t1/2?

A
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12
Q

Phase 1 and phase 2 of of drug metabolism?

A

Phase 1: carried out by cytochrome p450s (CYPs)

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13
Q

What is the most important CYP enzyme?

Where is it found within cells?

A

Found on the endoplasmic reticulum

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14
Q

What are the major phase 2 enzymes?

What is the purpose of phase 2 enzymes?

A
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15
Q

Explain prodrugs and why they might be beneficial

A
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16
Q

Explain what a metabolic shunt is

A

Can create a toxic metabolite if the wrong pathway is used

17
Q

Induction of CYP3A

A
18
Q

Why can you not use grapefruit in a lot of cases?

A