LG 6.11 - Pharmacokinetics Flashcards
1
Q
Define a drug’s pharmacokinetic profile?
A
- ADME
- Absorption
- Distribution
- Metabolism
- Excretion
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.
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.
4
Q
What is the first pass effect?
A
- Drug is being metabolized by liver before reaching systemic circulation.