Pharmacology: Volume of Distribution Flashcards

1
Q

processes that define time of drug in body

A
  • absorption
  • distribution
  • metabolism
  • clearance
  • collectively terminated pharmacokinetics
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2
Q

a “normal” person has how much water in their body

A
  • 45 L
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3
Q

breakdown of water in body

A
  • 30L in cells
  • 12 L in interstitial space
  • 3 L in plasma
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4
Q

how do most drugs reach their target sites if target is a receptor on outer cell surface

A
  • by traveling through the blood

- traverse endothelial cell layer to enter interstitial space

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5
Q

how do drugs reach their target sites if target molecule is intracellular?

A
  • by traveling through the blood
  • traverse endothelial cell layer to enter interstitial space
  • the drug will cross cellular plasma membrane to enter intracellular water compartment
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6
Q

which drugs are 100% absorbed?

A
  • IV drugs
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7
Q

volume of distribution

A
  • volume of total body water into which a drug partitions following distribution
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8
Q

at what Kg do we assume measurement for Vd?

A
  • 75 kg
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9
Q

if Vd is given as a ratio?

A
  • does not change per person

- but if given as liters, go back and get the ratio if you have to take it to different kilograms.

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10
Q

what drug freely moves across membranes

A
  • ethanol
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11
Q

acidic and basic drugs with low Vds

A
  • often associated with albumin and with alpha-1-acid glycoprotein
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12
Q

hydrophobic drugs with low Vds

A
  • found in plasma

- often associated with lipoproteins or globulins

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13
Q

average amount of total body water in each kilogram of body weight?

A
  • 0.6 L/kg
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14
Q

what reduces overall water content

A
  • increased body fat percentage

- older age

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15
Q

what increases overall water content

A
  • lower body fat percentage (athletes)

- young age

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16
Q

Vd formula

A

Vd = Q
Cp

Q = dose (in mg)
Cp = plasma concentration (mg/L)
17
Q

Vd higher than 45L?

A
  • the less drug that remains in the plasma, the higher the Vd will be.
18
Q

determines the pharmacokinetics of drug distribution

A
  • plasma protein binding
  • charge state
  • presence of drug transport molecules
  • drug solubility in different tissues
  • pH trapping
19
Q

drugs with a Vd of approximately 0.6 L/kg found

A
  • likely to be distributed all throughout body water compartments
20
Q

drugs with Vds higher than 0.6 L/kg

A
  • drawn out of plasma due to preferential accumulation in other tissues