Absorption of poorly soluble drug is

Related MCQs

• 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.
• Which of the following creates nonlinearity in drug distribution and not in drug absorption?
• Factors altering the binding of the drug to the blood increases the volume of distribution of the drug and the factors that influence drug binding to the extravascular component decreases the volume of distribution.
• Which of the following is a correct method to find the fraction of unbound drug in plasma? Given where Cu is the concentration of unbound drug and C is total plasma drug concentration.
• 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?
• Who has poorly developed BBB?
• Which of the following is a not mechanism of drug absorption through GIT
• Rate of absorption of drug by passive diffusion is maximum in
• Which of these absorption methods involves engulfing of the extracellular drug?
• In the sequence of events in the drug absorption from orally administered solid dosage, which one comes at first?