Chemistry Reference and  Research
           
 
Periodic Table
- standard table
- large table
 
Chemical Elements
- by name
- by symbol
- by atomic number
 
Chemical Properties
 
Chemical Reactions
 
Organic Chemistry
 
Branches of Chemistry
Analytical chemistry
Biochemistry
Computational Chemistry
Electrochemistry
Environmental chemistry
Geochemistry
Inorganic chemistry
Materials science
Medicinal chemistry
Nuclear chemistry
Organic chemistry
Pharmacology
Physical chemistry
Polymer chemistry
Supramolecular Chemistry
Thermochemistry

Volume of distribution

The volume of distribution (VD) is a pharmacological term used to quantify the distribution of a drug throughout the body after oral or intravenous dosing. It is defined as the volume in which the amount of drug would need to be uniformly distributed to produce the observed blood concentration. It is given by the equation:


{V_{D}} = \frac{total \ amount \ of \ drug \ in \ the \ body}{drug \ blood \ concentration}


The VD is not a real volume; it is more a reflection of how a drug will distribute throughout the body depending on several physicochemical properties, e.g. solubility, charge, size, etc. The VD may also be used to determine how readily a drug will displace into the body tissue compartments relative to the blood:

{V_{D}} = {V_{P}} + {V_{T}} \left(\frac{fu}{fu_{t}}\right)

Where:

VP = plasma volume

VT = apparent tissue volume

fu = fraction unbound in plasma

fuT = fraction unbound in tissue


Some examples:

Warfarin VD = 8L Reflects a high degree of plasma protein binding

Theophylline VD = 30L Represents distribution in total body water

Chloroquine VD = 15000L Shows highly lipophilic molecules which sequester into total body fat

01-04-2007 01:16:19
The contents of this article are licensed from Wikipedia.org under the GNU Free Documentation License. How to see transparent copy