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J Med Microbiol ; 58(Pt 9): 1203-1206, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19528175

ABSTRACT

The alarming spread of multiple drug resistance in Staphylococcus aureus, combined with the frequent occurrence of S. aureus and Staphylococcus epidermidis in biofilm-type infections, indicates a growing need for new therapies. The experimental steroidal amide anprocide [3beta-acetoxy-17beta-(l-prolyl)amino-5alpha-androstane] significantly reduced c.f.u. ml(-1) per suture (P <0.0001) in a murine model of topical S. aureus infection. In chequerboard assays with planktonic-grown S. aureus and S. epidermidis, anprocide was synergistic with bacitracin, oxacillin, clindamycin or ceftriaxone. Anprocide was also synergistic in combination with bacitracin or oxacillin against some isolates of biofilm-grown S. aureus and S. epidermidis.


Subject(s)
Androstanes/pharmacology , Anti-Bacterial Agents/pharmacology , Biofilms , Proline/analogs & derivatives , Staphylococcus aureus/drug effects , Staphylococcus aureus/physiology , Staphylococcus epidermidis/drug effects , Staphylococcus epidermidis/physiology , Androstanes/administration & dosage , Animals , Anti-Bacterial Agents/administration & dosage , Dose-Response Relationship, Drug , Mice , Proline/administration & dosage , Proline/pharmacology , Staphylococcal Skin Infections/drug therapy , Staphylococcal Skin Infections/microbiology
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