Senazol
Secnidazole is 5-nitroimidazole derivative, it has activity against
anaerobic bacteria and protozoa with properties similar to those of
metronidazole .
-Secnidazole enters micro–organisms by passive diffusion and
undergo activation by reduction of 5-nitro group .In anaerobic
micro –organisms such as Trichomonas, Giardia and Entamoeba
spp, this intracellular reduction occurs via the pyruvateferredoxin
oxidoreductase complex and result in concentration gradient
across the cell membrane which , in turn, enhance transport of the
parent drug into the cell. The electron affinity of the Secnidazole is
greater than that of reduced ferredoxin hence the drug interrupt the
normal electron flow.
- The mean absolute bioavailability of Secnidazole is 100% (+26%)
after oral administration of single doses of 0.5 to 2g and the
maximum plasma concentration occurs within3 hours.
- Secnidazole is rapidly, but not extensively, distributed in the body
after oral administration .
-Secnidazole crosses the placenta and can found in brest milk .
- The principle metabolite of Secnidazole RP 35843, is thought to
result from oxidation,persumably in the liver. No biological activity
has been reported for the metaboilte,
- Secnidazole does not appear to cause induction or inhibiton of
hepatic cytochrome P450 isoenzyme .
- The plasma elemination half life is about 25 hours.
- Secnidazole is mainly eleminated in urine (50% of the ingested
dose is excreted with 25 hours) .