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Notes in
Module 5 - Pharmacokinetics
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01/07/2024
Pharmacokinetics originate from the words "pharmakon" (drug/poison) and "kinesis" (movement). What questions are answered by this discipline?
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How is Kinetics different from dynamics?
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What are the four main processes in pharmacokinetics?
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What is elimination?
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What is disposition?
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What are the five major routes of administration?
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It is the transport of unmetabolized drug from site of administration into the plasma or circulatory system (in most cases)
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What are the three major modes of absorption?
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How is aqueous diffusion different from lipid diffusion?
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What two features are possible through carrier-mediated membrane transport?
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What four factors affect the efficacy of absorption?
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Ionized drugs are ___ while unionized drugs are ___
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Weak acids are better absorbed in ___ pH environments
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What are the ideal characteristics of a drug molecule for better absorption?
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What are the four common patient factors that affect drug absorption?
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Define distribution
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How is distribution related to efficacy and toxicity?
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What four factors affect drug distribution?
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What are the ideal characteristics of a drug with high distribution that make it easier to reach the target?
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It is the theoretical volume of fluid into which total drug administered would have to be diluted to produce the concentration in plasma
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What is the formula for Volume of distribution?
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Drugs that remain in blood have ___ Vd
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Define metabolism
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What are the two potential metabolic actions on a drug?
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How are phases of metabolism classified?
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Phase I Metabolism involves what processes?
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What is special about Cytochrome p450 enzymes?
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How are anti-epileptic and some TB medications metabolized?
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What processes are Phase II Metabolism involved with?
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What is special about glucuronidation?
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What processes are involved with Phase III Metabolism?
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Define excretion
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Passive diffusion is utilized by drugs that treat opioid overdose. How?
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Active tubular secretion is another type of excretion. What Phase of Metabolism does it primarily subserve?
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It is the amount of drug removed from the body per unit time (mg/h)
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It is the rate or flow of drug elimination of plasma volume per unit time (L/h)
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What are the four pharmacokinetic properties?
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It is the highest observed plasma drug concentration since administration of a single dose
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It is the time at maximum concentration
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It is the length of time before half the drug clears the body
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01/07/2024
It is a measure of drug exposure, usually computed by Trapezoidal Rule
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