Q. The principle of prodrug design is known as chemical formulation.

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Q. A drug which gets bio-transformed rapidly is known as a hard drug.

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Q. Which of the following will be a pharmaceutical application of prodrugs?

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Q. Which of the following will be the pharmacokinetic application of prodrugs?

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Q. How improvement of a drug in case of taste is done?

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Q. A liquid with high vapour pressure has a strong odour.

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Q. Which one of the following will be an example of changing the physical form of the drug to get a prodrug?

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Q. No drug cause damage to the gastric mucosa.

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Q. Which of the following reduces the pain of injection?

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Q. Which one of these is the best way to preserve drugs for intravenous use?

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Q. Why carbenicillin cannot be given orally?

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Q. Why lipophilic drugs are absorbed easily?

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Q. Which of the following is not a disadvantage of site-specific drug delivery?

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Q. Which of the following will not be a limitation for prodrug design?

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Q. How to prevent hepatic first-pass metabolism for corticosteroids?

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Q. Which one of the following is the principal organ for drug excretion?

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Q. Compounds excreted in bile is classified into 3 categories. Which one of the following does not come under the categories?

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Q. What is the molecular weight cut off for biliary excretion?

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Q. What is the equation for biliary clearance?

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Q. For a certain drug, the bile flow rate is 0.7 ml/mm, the biliary drug concentration is 2g/ml and the plasma drug concentration is 0.8g/ml. What will be the bile clearance?

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