Volume of distribution

In pharmacology, the volume of distribution (, also known as apparent volume of distribution or volume of dilution[1]) is 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.[2]

Roughly speaking, the , as a property of a drug, measures the degree to which it is distributed in body tissue rather than the blood plasma. Drug properties which cause high include high lipid solubility (non-polarity), low rates of ionization, or low plasma protein binding capabilities. Disease states which increase include kidney failure (due to fluid retention) and liver failure (due to altered body fluid and plasma protein binding). Conversely, dehydration may decrease .

The initial volume of distribution describes blood concentrations prior to attaining the apparent volume of distribution and uses the same formula.

  1. ^ Ward RM, Kern SE, Lugo RA (2012). "Pharmacokinetics, Pharmacodynamics, and Pharmacogenetics". Avery's Diseases of the Newborn. Elsevier. pp. 417–428. doi:10.1016/b978-1-4377-0134-0.10034-4. ISBN 978-1-4377-0134-0.
  2. ^ "Volume of distribution". sepia.unil.ch. Retrieved 19 April 2018.