Zack PharMa Flashcards

1
Q

Mechanisms of drug absorption?

A

1) simple passive diffusion- small hydrophobic drugs
2) facilitated diffusion
3) active transport
4) endocytosis

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2
Q

Most weak acid drugs are absorbed at what site of GI tract

A

Proximal duodenum or the gastro duodenal junction.

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3
Q

Weak bases are best absorbed at what part of the GI tract ?

A

Distal duodenum

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4
Q

In shock drugs administered IV: Why?

A

It is because the blood flow overall and in particular into the GI tract are reduced in shock. Therefore, drugs administered PO will not be absorbed adequately

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5
Q

What are the factors affecting drugs absorption?

A

1) Ph of the site of drug absorption.
2) blood flow
3) Total surface area and contact time available for the drug.
4) P glycoproteins ( seen in some people)which cause exocytosis of the drug back into the GI tract. It is one of the causes of multidrug resistance.

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6
Q

The formula for bioavailability is ?

A

F= AUC oral / AUC IV
F= bioavailability
AUC = area under the curve

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7
Q

Factors affecting bioavailability?

A

1) The solubility of the drug: The more hydrophobic and the smaller the drug, the more bioavailable it is.
2) instability of the drug: the drugs that are susceptible to degradation by GI PH or GI enzymes, if given orally will have poor bioavailability
3) First pass effect

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8
Q

For the best absorption of a weak base drug, the PH should be?

A

Very close to the Pka of the drug

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9
Q

Basic drugs are bound to what in plasma protein?

A

Alpha-01 acid glycoproteins

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