Lecture 1: Intro to ADME Flashcards

1
Q

ADME

A

-Absorption
-Distribution
-Metabolism
-Excretion

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2
Q

How to quantify drug effect

A

-Onset
-Duration
-Intensity

-determined by concentration vs time profile

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3
Q

Dosage form to effect

A

-release
-dissolution
-degradation
-absorption
-excretion
-distribution

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4
Q

Pharmacokinetics

A

study of ADME of xenobiotics

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5
Q

Pharmacodynamics

A

-study of EFFECTS and ACTION of xenobiotics

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6
Q

Minimum effective concentration range (MEC on graph)

A

concentration of drug that gives minimum effect

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7
Q

Duration

A

time the graph is above MEC

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8
Q

slide

A

10

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9
Q

drug disposition

A

fate of drug after entering systemic circulation

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10
Q

Pharmacotherapeutics

A

-pathophysiology
-pharmacodynamics
-pharmacokinetics

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11
Q

Routes of administration

A

-Ingestion
-Inhalation
-Dermal
-Parenteral (Injection)

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12
Q

Reduction in extent of absorption impacts

A

intensity

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13
Q

reduction in the speed of entry into systemic circulation impacts

A

onset

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14
Q

speed and extent of distribution impacted by

A

-barriers
-blood flow

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15
Q

Outcomes of metabolism

A

-active drug to inactive metabolite
-active to active
-inactive to active
-active to REactive

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16
Q

Routes of Excretion

A

-renal (primary) or Biliary to feces
-also pulmonary, salivary, mammary

17
Q

Which antibiotic would be the better choice in
a patient with renal failure?

-eliminated in bile
-eliminated in urine

A

eliminated in bile

18
Q

Why is ADME important

A

-use of preclinical models to predict ADME = lot less drug failure

19
Q

Active drug to inactive metabolite

A

phenobarbital to hydroxyphenobarbital by hydroxylation

20
Q

Active drug to active metabolite

A

procainamide to N-acetylprocainamide by acetylation

21
Q

inactive drug to active metabolite

A

codein to morphine by demthylation

22
Q

active drug t reavtive metabolite

A

-acetaminophen to reactive metabolite by

23
Q

Enteric coated aspirin

A

coating reliant on pH to dissolve
-WAIT until small intestine
= SLOWER