LG 6.11 - Pharmacokinetics Flashcards

1
Q

Define a drug’s pharmacokinetic profile?

A
  • ADME
  • Absorption
  • Distribution
  • Metabolism
  • Excretion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the difference between bioavailability and bioequivalence?

A
  • Bioavailability: fraction of drug reaching systemic circulation.
  • Bioequivalence: compares drug dosage form made by different manufacturers. Serum concentration time curves from the 2 products must be nearly superimposable, same peak level, time to peak level and AUC.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the effect by P-glycoprotein?

A
  • A common drug transporter; in GI tract, it can send absorbed drugs back into intestinal lumen, decreasing their absorption and bioavailability.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the first pass effect?

A
  • Drug is being metabolized by liver before reaching systemic circulation.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly