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PMID: 4202265 Published · ppublish English Clinical Trial Comparative Study Journal Article Randomized Controlled Trial

Cefoxitin, a new semi-synthetic cephamycin: an in-vitro and in-vivo comparison with cephalothin.

British medical journal ·Vol. 4 ·No. 5893 ·1973-12-15 ·Pages 653-5

Kosmidis J, Hamilton-Miller JM, Gilchrist JN, Kerry DW, Brumfitt W

Abstract

The activity of cefoxitin was compared with that of cephalothin against 229 bacterial strains. Cefoxitin was more active against most Gram-negative strains, notably against indole-producing Proteus spp., which are usually resistant to the cephalosporins. Cefoxitin was not susceptible to any significant extent to degradation by beta-lactamases produced by Gram-negative organisms. Against Gram-positive organisms, however, cefoxitin was considerably less active than cephalothin, but minimum inhibitory concentrations for Staphylococcus aureus were well within therapeutically attainable blood levels.Pharmacokinetic studies in 18 volunteers showed a higher and longer sustained antibiotic activity in serum and urine after injections of cefoxitin than after equal doses of cephalothin. Urinary recovery of cefoxitin activity was also much higher than that of cephalothin. No evidence of toxicity due to cefoxitin was found. Cefoxitin was slightly less painful after intramuscular injection than cephalothin.

MeSH Terms
Adolescent Adult Alcaligenes/drug effects Bacteroides/drug effects Carbamates/metabolism,pharmacology,toxicity Cephalosporins/metabolism,pharmacology,toxicity Cephalothin/metabolism,pharmacology Enterobacteriaceae/drug effects Enterococcus faecalis/drug effects Escherichia coli/drug effects Humans Injections, Intramuscular Injections, Intravenous Klebsiella/drug effects Male Microbial Sensitivity Tests Proteus/drug effects Proteus mirabilis/drug effects Staphylococcus/drug effects
Chemicals
Carbamates Cephalosporins Cephalothin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kosmidis J
Hamilton-Miller J M
Gilchrist J N
Kerry D W
Brumfitt W
References (6)
6 references, click to expand
  1. Semisynthetic cephalosporins via a novel acyl exchange reaction.
    J Am Chem Soc. 1972 Feb 23;94(4):1410-1 PMID: 5015670
  2. In vitro studies of cephanone, a 3-heterocyclic-thiomethyl cephalosporin derivative.
    J Antibiot (Tokyo). 1973 Mar;26(3):153-6 PMID: 4593238
  3. Cephanone: in vitro antibacterial activity and pharmacology in normal human volunteers.
    Antimicrob Agents Chemother. 1972 Oct;2(4):250-4 PMID: 4670495
  4. Cephamycins, a new family of beta-lactam antibiotics. I. Production by actinomycetes, including Streptomyces lactamdurans sp. n.
    Antimicrob Agents Chemother. 1972 Sep;2(3):122-31 PMID: 4790552
  5. Cephamycins, a new family of beta-lactam antibiotics: antibacterial activity and resistance to beta-lactamase degradation.
    Antimicrob Agents Chemother. 1973 Feb;3(2):254-61 PMID: 4790591
  6. Pharmacological and toxicological studies on cephalotin.
    Clin Med (Northfield). 1963 Jun;70:1123-38 PMID: 15445892
Article Info
Journal
British medical journal
Abbr.
Br Med J
ISSN
0007-1447
Published
1973-12-15
Pages
653-5
Language
English
Region
England
NLM ID
0372673
PMCID
PMC1587624
Subset
IM
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