Pharmaceutical Factors Flashcards

1
Q

What happens to the risk of bioavailability problems as you slow the rate of absorption of a drug?

A

Risk of bioavailability problems increases

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2
Q

Order the following drug preparations in order of rate of absorption: aqueous solutions, suspensions, coated tablets

A

Aqueous solutions absorbed fastest (lowest risk of bioavailability problems), then suspensions, then coated tablets absorbed slowest

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3
Q

Why do some drugs have an enteric coating (EC capsules e.g. Omeprazole)

A

To prevent them being digested in the stomach before they can take effect

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4
Q

What is the difference between ibuprofen and ibuprofen lysine?

A

Ibuprofen lysine absorbed more rapidly, but also has more rapid elimination due to shorter half life

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5
Q

Why are EC/enteric drugs useful? Give an example!

A

Prevent drug being dissolved immediately and prevent irritation of stomach e.g. oral steroids should have EC to avoid local effects on stomach

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6
Q

When are sustained release preparations (SR preparations) used? How to they work?

A

. When a drug has a short half-life but you need the drug to be released slowly over time
. Drug dissolved layer by later (like an onion) so drug can be released and absorbed by body more slowly over time

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7
Q

Morphine can come as a Morphogesic or as Oramorph. What is the difference between these forms?

A

. Morphogesis is SR drug to give continuous 12 hour pain relief
. Oramorph- suspension to provide breakthrough pain relief

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8
Q

What type of drug is Omeprazole?

A

Proton pump inhibitor

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9
Q

Why is Omeprazole given as an EC capsule?

A

Omeprazole is acid labile so would dissolve in stomach acid

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10
Q

What is Omeprazole used to treat? How does it work?

A

. Heartburn
. Capsule polymer breaks down in duodenum
. Drug absorbed in blood, inhibits PPs in parietal cells to inhibit secretion of HCl

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