Q. What will be the best definition for “carrier”?

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Q. What is the major difference between Facilitated diffusion and Passive diffusion?

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Q. What influences the permeation of drugs in an Ionic or Electrochemical diffusion?

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Q. Which kind of drugs are absorbed through endocytosis?

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Q. Which drugs are absorbed through pore transport?

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Q. Which types of drugs get absorbed by ion-pair transport?

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Q. Which of these absorption methods involves engulfing of the extracellular drug?

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Q. Which is the other name of “cell eating”?

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Q. Transfer of an endocytic vesicle from one extracellular compartment to another is known as _____________

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Q. A drug can be absorbed by more than one mechanism.

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Q. Which one of these is a physicochemical property of Drug substance?

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Q. Which one of these does not come under a physicochemical property of drugs?

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Q. In the sequence of events in the drug absorption from orally administered solid dosage, which one comes at first?

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Q. Which one is the correct sequence for drug absorption through the oral route?

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Q. Patient-related factors of drug absorption do not deal with which one of these?

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Q. The rate at which drug reaches the systemic circulation is determined by the slowest of the various steps involved in the sequence. This is known as ____________

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Q. Diffusion coefficient of drug D, Greater the value faster us the dissolution.

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Q. Greater the surface area lesser is the dissolution.

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Q. Which one of the following is a critical rate-limiting step of drug absorption?

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Q. Which sentence will define the Dissolution rate?

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