Q. Acidic drugs are best absorbed through the stomach and basic drugs are best absorbed through the intestine.

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Q. What could be the reason that irrespective of pH any drug gets absorbed mostly from the intestine?

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Q. Drug having a small partition coefficient can rapidly penetrate the lipid membrane but diffusion through the unstirred water layer is a rate-limiting step.

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Q. What are the major stability problems which result in poor bioavailability of any orally administered drugs?

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Q. Which form of drug formulation has disintegration time?

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Q. Which tablets have longer Disintegration time?

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Q. Disintegration time is directly proportional to the amount of binder present in the tablet.

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Q. Which of the following is not a form of excipients?

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Q. Which of the following is not a limitation granulation?

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Q. The agglomerative phase of the communication method grinds the drug in a ball mill for a long time to affect spontaneous agglomeration. But results showed tablets produced are softer.

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Q. Which of these is not a characteristic of tablet formulation by Agglomerative phase of the communication process?

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Q. What does the graph of Rate of Drug dissolution v/s Compression force with this type of curve interpret?

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Q. Capsules with bigger particles and intense packing have poor drug release and dissolution rate due to an increase in the pore size.

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Q. Which one of them is not a common form of excipients of drug manufacturing?

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Q. Vehicles are the solvent system for the liquefied drug. Which one of them is not an example of a kind of vehicle?

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Q. Which one of the following will be an example of organic diluents?

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Q. What is the function of a granulating agent in drug formulation?

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Q. What is the full form of PVP and what is its function in drug formation?

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Q. Which one of the following sentences depicts the function of Disintegrants correctly?

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Q. A large amount of binders tends to increase the hardness of tablets.

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