3) Pharmacokinetics/Dosing Schedule Flashcards

1
Q

Major processes involved in pharmacokinetics

A
  • Absorption
  • Distribution
  • Metabolism
  • WElimination
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2
Q

Apparent volume of distribution (Vd)

A
  • The theoretical volume that would be necessary to contain the total amount of an administered drug at the same concentration that it is observed in the blood plasma
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3
Q

Volume of distribution (Vd) is an important indicator of

A
  • The extent of drug distribution into body fluids and tissues
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4
Q

A large volume of distribution usually indicates

A
  • The drug distributes extensively into body tissues and fluids
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5
Q

Clearance (Cl)

A
  • The ratio of the rate of elimination of a drug to the concentration of the drug in the plasma or blood
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6
Q

Biodisposition

A
  • The processes of drug absorption, distribution, and elimination
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7
Q

Effective drug concentration

A
  • The concentration of a drug at the receptor site
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8
Q

Half life t1/2

A
  • The time required for the amount of drug in the body or blood to fall by 50% of its Cmax
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9
Q

Area under the curve (AUC)

A
  • The graphic area under a plot of drug concentration versus time after a single dose or during a single dosing interval
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10
Q

Bioavailability (F)

A
  • The fraction (or percentage) of the administered dose of drug that reaches the systemic circulation
  • Defined as unity (or 100%) in the case of intravenous administration
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11
Q

Drug extraction

A
  • The extraction of drug from the circulation by the liver is equal to blood flow (Q) times the difference between entering and leaving drug concentration, ie, Q × (Ci – Co).
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12
Q

Therapeutic window

A
  • The safe range between the minimum therapeutic concentration (determines the trough) and the minimum toxic concentration of a drug (determines the peak)
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13
Q

Dose regimen

A
  • Plan for drug administration over a period of time
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14
Q

To maintain the plasma concentration within a specified range over long periods of therapy

A
  • A schedule of maintenance doses is used
  • If it is necessary to achieve the target plasma level rapidly, a loading dose may be used to “load” the Vd with the drug
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15
Q

Maintenance dosage

A
  • Dose required for regular administration to maintain a target plasma level
  • Dosing rate = (CL x desired plasma concentration)/bioavailability
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16
Q

Loading dose

A
  • Dose required to achieve a specific plasma drug concentration level (Cp) with a single administration
  • Loading dose = (Vd x desired plasma concentration)/bioavailability