Indication |
For the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. |
Pharmacodynamics |
Amcinonide is a topical corticosteroid. The topical
corticosteroids constitute a class of primarily synthetic steroids used
as anti-inflammatory and antipruritic agents. Amcinonide reduces or
inhibits the actions of chemicals in the body that cause inflammation,
redness, and swelling. The mechanism of anti-inflammatory activity of
the topical corticosteroids is unclear. Various laboratory methods,
including vasoconstrictor assays, are used to compare and predict
potencies and/or clinical efficacies of the topical corticosteroids.
There is some evidence to suggest that a recognizable correlation exists
between vasoconstrictor potency and therapeutic efficacy in man. When
in an ointment form, amcinonide also helps the skin maintain moisture. |
Mechanism of action |
The mechanism of the anti-inflammatory activity of the topical
steroids, in general, is unclear. However, corticosteroids are thought
to act by the induction of phospholipase A2 inhibitory proteins,
collectively called lipocortins. It is postulated that these proteins
control the biosynthesis of potent mediators of inflammation such as
prostaglandins and leukotrienes by inhibiting the release of their
common precursor, arachidonic acid. Arachidonic acid is released from
membrane phospholipids by phospholipase A2. Amcinonide has affinity for
the glucocorticoid receptor. It has weak affinity for the progesterone
receptor, and virtually no affinity for the mineralocorticoid, estrogen,
or androgen receptors. |
Absorption |
Topical corticosteroids can be absorbed from normal intact skin.
Inflammation and/or other disease processes in the skin increase
percutaneous absorption. |
Volume of distribution |
Not Available |
Protein binding |
Not Available |
Metabolism |
Once absorbed through the skin, topical corticosteroids are
handled through pharmacokinetic pathways similar to systemically
administered corticosteroids. Corticosteroids are metabolized primarily
in the liver and are then excreted by the kidneys. |
Route of elimination |
Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys.
Some of the topical corticosteroids and their metabolites are also excreted into the bile. |
Half life |
Not Available |
Clearance |
Not Available |
Toxicity |
Results from acute toxicity studies do not indicate that any risk
of acute intoxication is to be expected following a single dermal
application of an overdose (application over a large area under
conditions favorable to absorption) or inadvertent oral ingestion. |