Q. Which drugs results in distortion of double stranded DNA structure?

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Q. Which one of the following factors related to protein-drug binding is not related to drugs?

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Q. Which one of the following factor related to protein-drug binding is not related to drug interactions with the binding site?

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Q. Which of the following factors for protein drug binding is a drug interaction factor?

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Q. Which drugs bind to HSA easily?

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Q. Which drugs easily bind to adipose tissue?

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Q. Which drug easily bind to AAG?

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Q. The extent of drug-protein binding can change with both changes in protein and drug concentration.

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Q. In the equation X= Vd C, what does X stands for?

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Q. Only unbound or free drug is capable of being eliminated.

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Q. Penicillin has short plasma half-life although it can bind to plasma protein rigidly.

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Q. Displacement interactions are significant in the case of drugs which are more than 95% bound.

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Q. Which of the following is a correct method to find the fraction of unbound drug in plasma? Given where Cu is the concentration of unbound drug and C is total plasma drug concentration.

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Q. What kind of graph is shown in the picture?

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Q. What kind of graph is shown in the picture?

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Q. What kind of graph is shown in the picture?

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