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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Q. An example of lubricants will be __________

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Q. The deleterious effect of various coatings on drug dissolution is shown in orders below. Which one of them is the correct order?

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Q. Which of the following will be an example of an organic suspending agent?

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Q. Which one of these is not a mechanism of the working of surfactants?

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Q. PABA complex is used for the enhancement of ______________

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Q. The concentration of colorant does not affect the drug solubility.

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Q. Suspending agents and some sugars can be used as viscosity imparters.

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Q. Which of the following will be the slowest step in tablet drug absorption?

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Q. Aging of dosage form affects drug release.

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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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