Q. Which form of the drug has the highest bioavailability?

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Q. Why emulsion dosage form for lipophilic drugs proved better?

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Q. Which is the major rate-limiting step in the absorption of a drug from suspension dosage?

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Q. Which coating is thin and dissolve rapidly?

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Q. Which option describes the function of the enteric coated drug?

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Q. Hydrophobic drug with fine particle size in capsule results in a decreasing porosity of powder bed.

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Q. Viscous fluids and oils are administered in hard gelatin capsules.

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Q. From the below options which will be the most widely used form of dosage?

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Q. What is the mean length of GIT?

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Q. The entire length of the GI is lined by ___________

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Q. Which drugs get absorbed in the stomach mostly?

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Q. Which drugs gets mostly absorbed from the mouth?

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Q. From the surface of villi protrude smaller projection known as __________

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Q. Which of the following sentences will be the actual definition of folds of Kerckring?

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Q. Which one of the following is not a characteristic for the small intestine?

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Q. How can we increase the time of gastric emptying?

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Q. What is the gastric emptying rate?

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Q. How can we study the gastric emptying of a given drug?

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Q. Up to how much the microvilli in the small intestine increases the relative surface area of the small intestine?

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Q. What is the main role of the large intestine?

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