Cefazolin Chemische Eigenschaften,Einsatz,Produktion Methoden
R-Sätze Betriebsanweisung:
R20/21/22:Gesundheitsschädlich beim Einatmen,Verschlucken und Berührung mit der Haut.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Beschreibung
Cefazolin has the natural acetyl side chain at C-3 replaced by a thio-linked thiadiazole ring. Although this
group is an activating leaving group, the moiety is not subject to the inactivating host hydrolysis reaction
that characterizes cephapirin. At C-7, it possesses a tetrazoylmethylene unit. Cefazolin is less irritating on
injection than its cohort in this generation of drugs and has a longer half-life than cephapirin. Its dosing
should be reduced in the presence of renal impairment. It is comparatively unstable and should be protected
from heat and light.
Chemische Eigenschaften
needles
Verwenden
Cefazolin is an antibacterial compound derived from 7-amino-cephalosporanic acid.
Definition
ChEBI: A cephalosporin compound having [(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl and (1H-tetrazol-1-ylacetyl)amino side-groups.
Antimicrobial activity
Enterobacter, Klebsiella, Providencia, Serratia spp.
and Pr. vulgaris are all resistant. B. fragilis is resistant, but
other anaerobes are susceptible.
Pharmakokinetik
Distribution
The volume of distribution is the smallest of the cephalosporins
in group 1, perhaps an indication of relative confinement
to the plasma space. It crosses inflamed synovial
membranes, but the levels achieved are well below those
of the simultaneous serum levels and entry to the CSF is
poor. In patients receiving 10 mg/kg by intravenous bolus,
mean concentrations in cancellous bone were 3.0 mg/kg
when the mean serum concentration was 33 mg/L, giving
a bone:serum ratio of 0.09. Some crosses the placenta,
but the concentrations found in the fetus and membranes
are low.
Metabolism and excretion
It is not metabolized. Around 60% of the dose is excreted
in the urine within the first 6 h, producing concentrations
in excess of 1 g/L. Excretion is depressed by probenecid.
The renal clearance is around 65 mL/min and declines in
renal failure, when the half-life may rise to 40 h, although levels
in the urine sufficient to inhibit most urinary pathogens
are still found. It is moderately well removed by hemodialysis
and less well by peritoneal dialysis.
Levels sufficient to inhibit a number of enteric organisms
likely to infect the biliary tract are found in T-tube bile (17–31
mg/L after a 1 g intravenous dose), but this is principally due
to the high serum levels of the drug and the total amounts
excreted via the bile are small.
Clinical Use
Cefazolin has been widely used in surgical prophylaxis,
especially in biliary tract (because of the moderately high
concentrations achieved in bile), orthopedic, cardiac and
gynecological surgery.
Nebenwirkungen
Side effects are those common to other cephalosporins
,including rare bleeding disorders and encephalopathy
in patients in whom impaired excretion or direct instillation
leads to very high CSF levels. Neutropenia has been
described and hypoprothrombinemic bleeding has been
attributed to the side chain.
Cefazolin Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
