Abstract |
In a murine model of systemic infection with methicillin-resistant Staphylococcus aureus (MRSA), J-111,225 showed an ED(50) value of 5. 83 mg/kg, which was comparable to vancomycin (ED(50) 4.84 mg/kg), whereas imipenem failed to cure infected mice (ED(50) >100 mg/kg). Against a mixed infection caused by MRSA and Pseudomonas aeruginosa, monotherapy with J-111,225 showed an ED(50) value of 7.23 mg/kg, whereas combined treatment with vancomycin plus imipenem (1:1) had an ED(50) of 20.86 mg/kg. J-111,225 showed good therapeutic efficacy against methicillin-susceptible S. aureus, penicillin-resistant Streptococcus pneumoniae, Escherichia coli, Klebsiella pneumoniae and P. aeruginosa. The unusually broad spectrum suggests that monotherapy with this novel carbapenem may be suitable for polymicrobial infections associated with MRSA.
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Authors | K Shibata, R Nagano, T Hashizume, H Morishima |
Journal | The Journal of antimicrobial chemotherapy
(J Antimicrob Chemother)
Vol. 45
Issue 3
Pg. 379-82
(Mar 2000)
ISSN: 0305-7453 [Print] England |
PMID | 10702562
(Publication Type: Journal Article)
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Chemical References |
- Anti-Bacterial Agents
- Carbapenems
- J 111225
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Topics |
- Animals
- Anti-Bacterial Agents
(pharmacokinetics, pharmacology, therapeutic use)
- Bacteria
(drug effects)
- Bacterial Infections
(drug therapy, metabolism, microbiology)
- Carbapenems
(pharmacokinetics, pharmacology, therapeutic use)
- Methicillin Resistance
- Mice
- Mice, Inbred ICR
- Microbial Sensitivity Tests
- Pseudomonas Infections
(drug therapy, microbiology)
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