In vitro evaluation of Ro 13-9904.
AUTOR(ES)
Hinkle, A M
RESUMO
The in vitro activity of a new investigational cephalosporin, Ro 13-9904, was compared with those of four cephalosporins (cephalothin, cefamandole, cefoxitin, and moxalactam), five semisynthetic penicillins (mezlocillin, piperacillin, carbenicillin, ticarcillin, and azlocillin), and the aminoglycoside tobramycin. Ro 13-9904 inhibited 75% of all isolates of Enterobacteriaceae at a concentration of 6.25 micrograms/ml, including Enterobacter spp., Serratia marcescens, and indole-positive Proteus spp. Ro 13-9904 was only minimally active against Pseudomonas aeruginosa and enterococci. There was no significant change (greater than or equal to 2 dilutions) in drug activity when tested in various pH and media. A significant inoculum effect occurred when the size of the inoculum was increased from a concentration of 10(5) to 10(7) organisms per ml.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=284051Documentos Relacionados
- In vitro susceptibility of Salmonella to various antimicrobial agents, including a new cephalosporin, Ro 13-9904.
- Comparative in vitro studies of Ro 13-9904, a new cephalosporin derivative.
- Ceftriaxone (Ro 13-9904) therapy of serious infection.
- In vitro activity of Ro 13-9904, a new beta-lactamase-stable cephalosporin.
- Pharmacokinetics of Ro 13-9904, a broad-spectrum cephalosporin.