is the maximum (or peak)
serum concentration
In chemistry, concentration is the abundance of a constituent divided by the total volume of a mixture. Several types of mathematical description can be distinguished: '' mass concentration'', '' molar concentration'', '' number concentration'', ...
that a drug achieves in a specified
compartment or test area of the body after the drug has been administered and before the administration of a second dose.
It is a standard measurement in
pharmacokinetics.
Description
is the opposite of , which is the minimum (or trough) concentration that a drug achieves after dosing. The related pharmacokinetic parameter is the time at which the is observed.
After an intravenous administration, and are closely dependent on the experimental protocol, since the concentrations are always decreasing after the dose. But after oral administration, and are dependent on the extent, and the rate of drug absorption and the disposition profile of the drug. They could be used to characterize the properties of different formulations in the same subject.
Short term drug
side effect
In medicine, a side effect is an effect of the use of a medicinal drug or other treatment, usually adverse but sometimes beneficial, that is unintended. Herbal and traditional medicines also have side effects.
A drug or procedure usually use ...
s are most likely to occur at or near the , whereas the therapeutic effect of drug with sustained duration of action usually occurs at concentrations slightly above the .
The is often measured in an effort to show
bioequivalence (BE) between a generic and innovator drug product.
According to the FDA, drug quality
bioavailability (BA) and BE rely on pharmacokinetic measurements such as
AUC and that are reflective of systemic exposure.
See also
*
Cavg (pharmacology)
*
Area under the curve (pharmacokinetics)
References
{{Reflist
Pharmacokinetic metrics