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<i>In vitro</i> Assessment of Tobramycin, a new Aminoglycoside with Anti-<i>Pseudomonas</i> Activity
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1973
Year
Antibacterial AgentsStaphylococcus AureusVariable SusceptibilityAntimicrobial ChemotherapyAntibiotic ResistanceDrug ResistanceAntimicrobial StewardshipAntimicrobial TherapyAntibacterial MechanismsAnti-infective AgentsAntimicrobial ResistanceHealth SciencesPseudomonas SpeciesAntimicrobial Drug DiscoveryAntibacterial AgentAntimicrobial PharmacokineticsAntimicrobial CompoundNew AminoglycosidePharmacologyClinical MicrobiologyAntimicrobial SusceptibilityAntibioticsMicrobiologyAntimicrobial AgentsAntimicrobial PharmacodynamicsMedicine
In vitro studies of tobramycin showed it to be 2- to 4-fold more active than gentamicin against Pseudomonas species. 55 of 56 strains were inhibited by 2.5 μg of tobramycin/ml. Other gram-negative bacteria showed variable susceptibility to the drug. Strains of Staphylococcus aureus were generally inhibited by, and enterococci were generally resistant to 5 μg of tobramycin/ml. The effect of serum and of NaCl in the medium were studied. Combinations of tobramycin with carbenicillin gave conflicting results when examined for synergism against Pseudomonas by two different methods. Tobramycin failed to show synergism with penicillin against enterococci.