Pharmacokinetics 1 Flashcards

1
Q

the diffusion coefficient ?

A

1 / square root of the molecular weight

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2
Q

uptake of molecule into blood

A

discussion if lipid soluble and uncharged, carrier or channel or pinocytosis if large

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3
Q

ways of administering drug

A

intravenous - quickest avoids metablism
oral - into gut, metabolism enzymes
rectal - avoid gut
intramuscular - avoid git, e.g. insulin
intrathecal - into CSF e.g. lumbar puncture
inhalation - out and in same way may breath it out

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4
Q

What may affect absorption of drug

A

site administere, molecular weight, lipid solubility, pH, ionisation

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5
Q

pka?

A

used to calculate how much drug charged and how much non charged - only uncharged can cross lipid membranes to other compartments

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6
Q

Weak acid drug (aspirin 3.5 pH) in alkaline solution

A

will dissociate and be trapped in compartment

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7
Q

weak base in an acidic solution

A

will dissociate and trapped

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8
Q

how do you trap a weak acid in a compartment ?

A

give sodium carbonate

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9
Q

metformin where is it and what is the transporter

A

in hepatocytes, transported by OCT1

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10
Q

Ways receptor can be desensitised -

A

decrease coupling with ligand, no longer produces signal, receptor loss

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