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Cephalothin clearance of Staphylococcus aureus from two experimental infection sites in the presence and absence of local phagocytic cells.

Abstract
The clearance of Staphylococcus aureus from perforated peritoneal capsules which are accessible to phagocytic cells, and subcutaneous Visking chambers which exclude phagocytes, was studied simultaneously in eight rabbits implanted with both devices. Animals were treated with cephalothin, 100 mg/kg im every 8 h for sixteen doses, beginning 24 h after inoculation of the infection sites with S. aureus (cephalothin MIC 0.125 mg/l, MBC 0.5 mg/l). At the start of cephalothin, subcutaneous chambers contained a higher concentration of S. aureus (8.4 log10 cfu/ml) than peritoneal capsules (6.8 log10 cfu/ml, P less than 0.001). There was a significant bactericidal effect in subcutaneous chambers on both the third and sixth day of treatment (P less than 0.002), whereas in peritoneal capsules this did not occur until day six. The total reduction in bacterial count in subcutaneous chambers (7.0 log10 cfu/ml) was significantly greater than in capsules (4.4 log10 cfu/ml, P less than 0.002). The mean concentration of cephalothin in subcutaneous chambers (10.7 mg/l) was significantly higher than in peritoneal capsules (6.1 mg/l, P less than 0.02), but no difference in in-vitro killing of S. aureus was detected at these concentrations. We conclude that cephalothin clearance of S. aureus from a site accessible to phagocytes was delayed when compared to a phagocyte-inaccessible site.
AuthorsD N Gerding, B Bean, L R Peterson, J Moody, K Bettin
JournalThe Journal of antimicrobial chemotherapy (J Antimicrob Chemother) Vol. 20 Issue 5 Pg. 685-95 (Nov 1987) ISSN: 0305-7453 [Print] England
PMID3429371 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Cephalothin
Topics
  • Animals
  • Cephalothin (metabolism, pharmacology)
  • Female
  • Hydrogen-Ion Concentration
  • Leukocyte Count
  • Microbial Sensitivity Tests
  • Phagocytes (physiology)
  • Rabbits
  • Staphylococcal Infections (metabolism, microbiology)
  • Staphylococcus aureus (drug effects, metabolism)

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