Which of the following is a not mechanism of drug absorption through GIT

Related MCQs

• Which of the following creates nonlinearity in drug distribution and not in drug absorption?
• 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 one of the following physicochemical property is more important for passive diffusion of drugs from the GIT?
• 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.
• What is the mean length of GIT?
• 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.
• 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?
• Which one is the correct sequence for drug absorption through the oral route?
• Which kind of absorption mechanism is showing in the picture?
• Patient-related factors of drug absorption do not deal with which one of these?