drug disposition & fate of drugs 2 Flashcards

1
Q

Defines the volume of fluid that must be processed by organs of elimination

A

volumes of distribution

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2
Q

represents the plasma concentration at the time of drug administration (usually used in intravenous administration).

A

Cp0

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3
Q

Units of Volume of distribution

A

Liters or milliliters (describing the whole animal)
Liters/kg or milliliters/kg (normalized to body weight)

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3
Q

equation of volume of distribution

A

Vd=amount of drug/drug concentration in the plasma

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4
Q

is the sum of all organ clearances

A

Total body clearance (Clt)

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4
Q

specifically refers to the volume of plasma water cleared of the drug by the liver.

A

Hepatic clearance or CLEARANCE

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5
Q

The fraction of the volume of distribution cleared per unit time.

A

Rate constant of elimination

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6
Q

The time for elimination of one half of the total amount in the body.

A

Elimination Half – Life

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7
Q

refers to the half-life of a drug.

A

T1/2

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7
Q

half-life of gentamicin

A

2 to 3 hours in individuals with normal kidney function

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8
Q

is an itital dose of drug given to shorten the time to reach the steady-state concentrations.

A

loading dose

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9
Q

When a drug is administered by any route OTHER than IV, it is rare that the entire dose is absorbed

A

Fraction of dose absorbed.

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9
Q

Two drug products are bioequivalent if the nature and extent of therapeutic
and toxic effects are equal following administration

A

true

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9
Q

Attempt to describe the actual events which control drug absorption, distribution, and elimination

A

physiologic models

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9
Q

Attempt to accurately predict the time course of drug concentrations in one
(usually blood or plasma) or two (urine as well) body fluids.

A

Mathematic Models

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9
Q

Bioavailability is a measure of how much of a drug enters the bloodstream.

A

bioavailability

9
Q

wo drug products are considered bioequivalent when they have the same therapeutic and toxic effects after administration

A

bioequivalence

9
Q

These models are used to understand drug absorption, distribution, and elimination. There are physiologic models that describe real events in the body and mathematical models that predict drug concentrations over time

A

Pharmacokinetic Models:

9
Q

drugs can distribute in different body compartments, like the central compartment , peripheral compartment , and deep compartments

A

Body compartments

9
Q

2 central compartment

A

blood
elimination organs

9
Q

3 peripheral compartments

A

muscle
subcutaneous tissue
lung

9
Q

2 deep compartments

A

fat
kidney

9
Q

In this practice, _______often simplifies drug distribution to a one-compartment model.

A

clinical monitoring

9
Q

Relationship between dose and concentration/effects is linear. If you double the dose, concentrations/effects also double.

A

dose-independent behavior

9
Q

Absorption rate decreases as dose increases.

A

dose dependent absorption

10
Q

A fraction the dose of drug is absorbed per unit time.

A

First Order

11
Q

A constant amount of drug is eliminated per time

A

zero order

12
Q
A