Questions and Answers
What is the main target in pharmacokinetics?
Plasma/blood drug concentration between MEC and MTC
What is the theoretical framework for determining the time course of drug absorption, distribution, metabolism, and excretion?
Pharmacokinetics
What must the desired steady-state Cp be in order to be effective clinically but not toxic?
Greater than MEC and less than MTC
What does the pharmacokinetic model translate the dose into?
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What does the pharmacodynamic model convert Ce into?
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What does Cp typically correspond with in terms of drug effect?
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In the LADME scheme, what does 'Liberation' refer to?
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What are the dynamic processes reflecting following drug administration by any route?
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What is critical to the development of various drug delivery technologies?
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In case a drug is administered directly into the systemic circulation, what happens to the absorption process?
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