Q. Dissolution test apparatus I as per IP is…..
✅ Correct Answer: (A)
Paddle
Biopharmaceutics and Pharmacokinetic MCQs and Notes
Q. The drug concentration between MEC and MSC represents the….
✅ Correct Answer: (B)
Therapeutic range
Q. The rate of drug bioavailability is most rapid when the drug is formulated as a…..
✅ Correct Answer: (D)
solution
Q. Bioavailability is defined as…..
✅ Correct Answer: (D)
Rate and extent of absorption
Q. The reasons determining bioavailability are…..
✅ Correct Answer: (C)
Extent of absorption and hepatic first-pass effect
Q. The term bioavailability refers to the………….
✅ Correct Answer: (B)
measurement of the rate and amount of therapeutically active drug that reaches the systemic circulation
Q. …………decreases bioavailability of tetracycline.
✅ Correct Answer: (B)
DCP
Q. What would be the order of greater or lesser bioavailability of the dosage forms?
✅ Correct Answer: (B)
Intravenous > oral > rectal > topical
Q. If the Relative Bioavailability is 1, it indicates:
✅ Correct Answer: (A)
Bioavailability of dosage form of one drug is same as that of the other dosage form
Q. Comparison of the rate and extent of the absorption of drug from the formulation under study to the data of a reference standard that is given intravenously is known as:
✅ Correct Answer: (C)
Absolute bioavailability