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Questions and Answers
What is dose-dependent pharmacokinetics also termed as?
What may cause deviations from the linear pharmacokinetic profile observed with single low doses of a drug?
What happens to the pharmacokinetic parameters with the size of the administered dose in nonlinear pharmacokinetics?
What specialized processes may become saturated for drugs given at therapeutic levels?
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What may alter biliary excretion and cause non-linear pharmacokinetic behavior?
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What may cause renal nephrotoxicity and alter renal drug excretion, leading to non-linear pharmacokinetic behavior?
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Which type of kinetics transforms into a mixture of first-order and zero-order rate processes?
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What is one of the objectives of understanding non-linear pharmacokinetics?
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In linear pharmacokinetic models, what did it assume about the pharmacokinetic parameters for a drug when different doses were given?
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What are most of the processes of drug absorption, distribution, biotransformation, and excretion involving in non-linear pharmacokinetics?
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What are some causes of non-linear pharmacokinetic behavior?
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What specialized processes may become saturated for drugs given at therapeutic levels?
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What is dose-dependent pharmacokinetics also termed as?
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What happens to the pharmacokinetic parameters with the size of the administered dose in nonlinear pharmacokinetics?
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What are some causes of non-linear pharmacokinetic behavior?
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In linear pharmacokinetic models, what did it assume about the pharmacokinetic parameters for a drug when different doses were given?
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What may cause deviations from the linear pharmacokinetic profile observed with single low doses of a drug?
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What are most of the processes of drug absorption, distribution, biotransformation, and excretion involving in non-linear pharmacokinetics?
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What is one of the objectives of understanding non-linear pharmacokinetics?
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What type of kinetics do drugs exhibit when the elimination of the drug does not follow simple first-order kinetics?
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What is the term used to describe the rate constant at low plasma concentration where first-order kinetics is expected?
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What characteristic is exhibited by drugs that produce plasma drug concentrations well below the Km for all carrier-mediated enzyme systems affecting the pharmacokinetics of the drug?
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Which process may be affected by other drugs that require the same enzyme or carrier-mediated system in drugs exhibiting saturation kinetics?
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What characteristic is exhibited by drugs that demonstrate saturation kinetics regarding their elimination half-life as the dose is increased?
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What characteristic do drugs exhibit in the saturation kinetics?
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Which characteristic describes the plasma level-time curve for a drug that exhibits saturable kinetics when a large dose is given?
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What process describes the elimination of drug by a saturable enzymatic process according to Michaelis-Menten kinetics?
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At high plasma concentrations, what type of kinetics are not seen in drugs given in therapeutic doses?
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What happens to the elimination kinetics with very small doses of drugs such as salicylate and phenytoin?
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Which of the following drugs is reported to exhibit capacity limited elimination?
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What characteristic is exhibited by drugs that demonstrate saturation kinetics regarding their elimination half-life as the dose is increased?
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What type of kinetics do drugs exhibit when the elimination of the drug does not follow simple first-order kinetics?
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What process describes the elimination of drug by a saturable enzymatic process according to Michaelis-Menten kinetics?
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At high plasma concentrations, what type of kinetics are not seen in drugs given in therapeutic doses?
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What are some causes of non-linear pharmacokinetic behavior?
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Which characteristic describes the plasma level-time curve for a drug that exhibits saturable kinetics when a large dose is given?
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What specialized processes may become saturated for drugs given at therapeutic levels?
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What may cause renal nephrotoxicity and alter renal drug excretion, leading to non-linear pharmacokinetic behavior?
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What type of kinetics do drugs exhibit when the elimination of the drug does not follow simple first-order kinetics?
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What is one of the causes of non-linear pharmacokinetic behavior?
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What is dose-dependent pharmacokinetics also termed as?
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In linear pharmacokinetic models, what did it assume about the pharmacokinetic parameters for a drug when different doses were given?
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What process describes the elimination of a drug by a saturable enzymatic process according to Michaelis-Menten kinetics?
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What happens to the elimination kinetics with very small doses of drugs such as salicylate and phenytoin?
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Study Notes
Dose-Dependent Pharmacokinetics
- Also termed as nonlinear pharmacokinetics
Non-Linear Pharmacokinetic Behavior
- Caused by deviations from the linear pharmacokinetic profile observed with single low doses of a drug
- May occur due to saturation of specialized processes, such as enzymatic reactions or active transport, at therapeutic levels
- Can be altered by biliary excretion and renal nephrotoxicity
- Processes of drug absorption, distribution, biotransformation, and excretion may involve non-linear pharmacokinetics
Pharmacokinetic Parameters
- In nonlinear pharmacokinetics, parameters change with the size of the administered dose
- In linear pharmacokinetic models, parameters are assumed to remain constant with different doses
Objectives of Understanding Non-Linear Pharmacokinetics
- To predict pharmacokinetic behavior at high doses or with prolonged administration
Saturation Kinetics
- Type of kinetics that transforms into a mixture of first-order and zero-order rate processes
- Characterized by a decrease in elimination half-life as the dose is increased
- Plasma level-time curve exhibits a plateau or sigmoid shape when a large dose is given
- Process describes the elimination of drug by a saturable enzymatic process according to Michaelis-Menten kinetics
Special Cases
- Phenytoin and salicylate exhibit capacity-limited elimination, where elimination kinetics change with very small doses
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Description
Test your knowledge of dose-dependent pharmacokinetics, capacity-limited kinetics, and causes of non-linear pharmacokinetic behavior. Explore how increased doses or chronic medication can lead to deviations from the linear pharmacokinetic profile observed with single low doses.