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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Q. What should be the ideal solubility rate of an orally administered drug in the pH range of 2 to 8?

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Q. Which one of these is not a theory of Drug dissolution?

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Q. Which theory takes into account that a thin film is created by the solution of the solid at the solid-liquid interface?

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Q. In the equation G=Ki (Cs-Cb), what does G stands for______________

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Q. Which model does not approve the existence of the stagnant layer in the solid-liquid interface?

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Q. What does the interfacial barrier model states?

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Q. In the equation, Wo1/3-W1/3=Kt, K stands for ____________

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Q. Which are the two rate-determining step of drug absorption when given orally?

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Q. The maximum amount of solute dissolved in a given solvent under standard conditions of temperature, pressure, and pH is known as __________

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Q. In the equation, V dC/dt = dm/dt = A(Cs-Cb).√ γ D, what does γ stands for?

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Q. Each face of the crystal has a different interfacial barrier.

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