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Questions and Answers
Quelle est la formule pour calculer t1/2 dans une infusion proportionnelle?
Quelle est la formule pour calculer t1/2 dans une infusion proportionnelle?
Quel est l'exemple de médicament cité dans le texte pour illustrer la nécessité d'une concentration plasmatique stable?
Quel est l'exemple de médicament cité dans le texte pour illustrer la nécessité d'une concentration plasmatique stable?
Quel est l'impact du volume de distribution sur la concentration à l'état d'équilibre?
Quel est l'impact du volume de distribution sur la concentration à l'état d'équilibre?
Quel est l'impact du volume de distribution sur le temps nécessaire pour atteindre l'état d'équilibre?
Quel est l'impact du volume de distribution sur le temps nécessaire pour atteindre l'état d'équilibre?
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Qu'est-ce que la biodisponibilité?
Qu'est-ce que la biodisponibilité?
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Qu'est-ce que la bioéquivalence considère?
Qu'est-ce que la bioéquivalence considère?
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Quand se produisent les cinétiques non linéaires?
Quand se produisent les cinétiques non linéaires?
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Les cinétiques non linéaires ont-elles un état d'équilibre?
Les cinétiques non linéaires ont-elles un état d'équilibre?
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À quoi sert la dose de charge?
À quoi sert la dose de charge?
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Study Notes
- The text discusses the need for drugs to have stable plasma concentrations.
- The drug should be active at low plasma concentrations.
- The example given is the fentanyl patch.
- The speed of passage depends on something that is not specified in the text.
- The formula for calculating t1/2 in proportional infusion is 0.693 Vd/Kél.
- In bolus injection, less than 1% of the Ci remains in the blood after 7 half-lives.
- In continuous administration, steady state is reached after 4 half-lives.
- At the start, more medication is injected than eliminated.
- At steady state, medication elimination and injection are equal.
- Changing the medication concentration affects administration.
- The steady state concentration is the administration rate divided by clearance.
- The volume of distribution does not affect the steady state concentration.
- The volume of distribution impacts the time to reach the steady state.
- Two-compartment models have a central and peripheral compartment.
- Biodisponibility is the fraction of the dose that reaches the systemic circulation.
- Bioequivalence considers AUC, Cmax, and Tmax.
- Non-linear kinetics are rare and occur when metabolism is saturated.
- Non-linear kinetics do not have a steady state.
- The dose of charge can be used to reach the steady state faster.
- The steady state concentration is proportional to the dose given.
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Description
Test your knowledge on pharmacokinetics with this quiz! From understanding the importance of stable plasma concentrations to the formula for calculating t1/2 in proportional infusion, this quiz covers key concepts in drug administration. You'll also learn about the impact of volume of distribution, two-compartment models, and non-linear kinetics on drug administration. Sharpen your skills and see how much you know about pharmacokinetics!