In vitro dissolution rate studies on drug product are useful in bioavailability evaluation if they are correlated with

Related MCQs

• In vitro determination of bioavailability by dissolution rate is not the best way to determine therapeutic efficacy.
• The occurrence of food in the GI tract can affect the drug bioavailability from an oral drug product. The above give statement is?
• The rate of drug bioavailability is most rapid when the drug is formulated as a…..
• Bioavailability differences among oral formulations of a drug are most likely to occur if the drug
• Absorption of drugs can be categorized into 2 classes, physicochemical properties of drugs and Dosage form of the drug, on the basis of drug dissolution.
• For a certain drug, the bile flow rate is 0.7 ml/mm, the biliary drug concentration is 2g/ml and the plasma drug concentration is 0.8g/ml. What will be the bile clearance?
• What will be the rate of filtration if the rate of secretion is 0.9 ml/ sec, rate of reabsorption is 0.2 ml/sec and the rate of excretion is 2ml/sec for a particular drug?
• Which of the following is not an objective of bioavailability studies?
• Single-dose bioavailability studies are simple and common.
• Absolute surface area is proportional to the dissolution rate of a drug.