|
|
|
|
|
AzithromycinAzithromycin is the first macrolide antibiotic belonging to the azalide group. Azithromycin is derived from erythromycin by adding a nitrogen atom into the lactone ring of erythromycin A, thus making lactone ring 15-membered. Azithromycin is sold under the brand name of Zithromax and Sumamed, and is one of the world's best selling antibiotics. Azithromycin is used for the treatment of respiratory tract, soft-tissue and genitourinary infections. gcolor="#ffffff" align="center" colspan=2|
Azithromycin | | lign="center" colspan=2 style="border-bottom:3px solid gray;"|9-deoxy-9a-aza-9a-methyl-9a-homoerythromycin A | | gcolor="#efefef"| Molecular Weight | bgcolor="#dfefff"|748.88 | | gcolor="#efefef"|Empiric Formula | bgcolor="#dfefff"|C38H72N2 O12 | | gcolor="#efefef"|ATC code | bgcolor="#dfefff"|J01FA10 | | gcolor="#efefef"|Metabolism | bgcolor="#dfefff"|Liver | | gcolor="#efefef"| Pregnancy category | bgcolor="#dfefff"|B (USA)
B1 (Aus) | Etymology Azithromycin's name is derived from the azane-substituent and erythromycin. Its accurate chemical name is 2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[ (2,6-dideoxy-3-C-methyl-3-O -methyl-a-L-ribo-hexopyranosyl)oxy]-2-ethyl-3,4,10- trihydroxy-3,5,6,8,10,12,14-heptamethyl-11- [[3,4,6-trideoxy-3-(dimethylamino)-b-D- xylo-hexopyranosyl]oxy]-1-oxa-6- azacyclopentadecan-15-one. History A team of Pliva's researchers, Gabrijela Kobrehel, Gorjana Radobolja-Lazarevski and Zrinka Tamburasev led by Dr Slobodan Dokic, discovered azithromycin in 1980. It was patented in 1981, and was later found by Pfizer's scientists while going through patent documents. In 1986 Pliva and Pfizer signed a licensing agreement, which gave Pfizer exclusive rights for the sale of azithromycin in the Western Europe and United States. Pliva brought their azithromycin on the market in Central and Eastern Europe under the brand name of Sumamed in 1988, and Pfizer Zithromax in 1991. Available forms Azithromycin is commonly administered in tablet or oral suspension. It is also available for intravenous injection. Mechanism of action Azithromycin prevents bacteria from growing, by interfering with their protein synthesis. Azithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Azithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain gram-negative bacteria, particularly Hemophilus influenzae. Pharmacokinetics Unlike erythromycin, azithromycin is acid-stable and can therefore be taken orally without being protected from gastric acids. It is readily absorbed, and diffused into most tissues and phagocytes. Due to the high concentration in phagocytes, azithromycin is actively transported to the site of infection. During active phagocytosis, large concentrations of azithromycin are released. The concentration of azithromycin in the tissues can be over 50 times higher than in plasma. This is due to ion trapping and the high lipid solubility. Metabolism Azithromycin's half-life is approximately 2 days, and it's fairly resistant to metabolic inactivation. Its main elimination route is through excretion in to the biliary fluid, and some can also be eliminated through urinary excretion. Azithromycin is excreted through both of these elimination routes mainly in unchanged form. Side effects Most common side-effects are gastrointestinal; diarrhea, nausea, abdominal pain and vomiting.
|
 |
|
| Copyright 2005-2009 OnPedia.com. All Rights Reserved |
|
|