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PMID: 4670437 Published · ppublish English Comparative Study Journal Article

Comparative activity of sisomicin, gentamicin, kanamycin, and tobramycin.

Antimicrobial agents and chemotherapy ·Vol. 2 ·No. 6 ·1972-12-00 ·Pages 431-7

Waitz JA, Moss EL, Drube CG, Weinstein MJ

Abstract

Gentamicin, sisomicin, tobramycin, and kanamycin were compared in parallel tests in vitro and in vivo against a variety of bacterial strains and species. A number of differences were seen in vitro, in particular: (i) the lower activity of kanamycin, (ii) the greater activity of tobramycin against Pseudomonas, (iii) the greater activity of gentamicin and sisomicin against Serratia, and (iv) the generally similar results with tobramycin, gentamicin, and sisomicin against species other than Pseudomonas and Serratia, with the ranking in order of decreasing activity being sisomicin, gentamicin, and tobramycin. Analysis of disc test results suggested that the gentamicin disc is not adequate for testing the susceptibility of all bacteria to sisomicin or tobramycin. In vivo tests did not confirm all specifics of in vitro tests; results of in vivo tests indicated that sisomicin may be the most active. It is suggested that the place of each of the antibiotics in human therapy can best be evaluated by more rigorous in vivo tests and clinical studies rather than extensive in vitro comparisons.

MeSH Terms
Aminoglycosides/pharmacology Animals Anti-Bacterial Agents/pharmacology Bacteria/drug effects Bacterial Infections/drug therapy Gentamicins/pharmacology Kanamycin/pharmacology Male Mice Microbial Sensitivity Tests
Chemicals
Aminoglycosides Anti-Bacterial Agents Gentamicins Kanamycin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Waitz J A
Moss E L
Drube C G
Weinstein M J
References (9)
9 references, click to expand
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1972-12-00
Pages
431-7
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC444335
Subset
IM
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