Which one of these is not an approach to make the drug cross the blood-brain barrier?

Related MCQs

• 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.
• 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 of the following drug cannot pass through the plasma membrane barrier?
• What reasons make tissue-drug binding important for drug distribution?
• Which cell make up the blood-brain barrier?
• Which one of the following factor related to protein-drug binding is not related to drug interactions with the binding site?
• Which of the following creates nonlinearity in drug distribution and not in drug absorption?
• Patient-related factors of drug absorption do not deal with which one of these?
• Which one of these is not a theory of Drug dissolution?