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Clinical pharmacokinetics of carbenicillin, carfecillin, ticarcillin and BL-P 1654 in dairy cows.

Abstract
The minimal inhibitory concentrations (MIC) of carbenicillin, ticarcillin and BL-P 1654 for gram-negative udder pathogens were determined using the agar plate dilution method. The MIC of the drugs for 50% and 90% of the isolates examined ranged for Escherichia coli and Aerobacter spp. from 1.56 to 25 micrograms/ml, and for Klebsiella spp. and Pseudomonas spp. from 3.12 to 50 micrograms/ml. The Serratia spp. were relatively non-susceptible for the drugs studied (MIC greater than 50 micrograms/ml). Each drug was administered intravenously at 5 g and 15 g per cow to different groups of cows with normal and inflamed quarters of the udder. Distribution and elimination kinetic parameters calculated from serum drug level data were very similar to those of other beta-lactam antibiotics. Although drug concentrations in milk from inflamed quarters were higher than in milk from normal quarters, they were considerably below the MIC for the majority of gram-negative udder pathogens. The data suggest that parenteral treatment of gram-negative udder infections with carbenicillin, carfecillin, ticarcillin and BL-P 1654 at the dose levels used in the present study is unlikely to result in a bacteriological cure and would probably be clinically ineffective.
AuthorsJ F Nouws, G Ziv, C A Van Ginneken, T B Vree
JournalJournal of veterinary pharmacology and therapeutics (J Vet Pharmacol Ther) Vol. 7 Issue 1 Pg. 35-43 (Mar 1984) ISSN: 0140-7783 [Print] England
PMID6323731 (Publication Type: Journal Article)
Chemical References
  • Penicillins
  • BLP 1654
  • Penicillanic Acid
  • Carfecillin
  • Ticarcillin
  • Carbenicillin
Topics
  • Animals
  • Carbenicillin (analogs & derivatives, metabolism)
  • Carfecillin (metabolism)
  • Cattle
  • Enterobacteriaceae (drug effects)
  • Female
  • Kinetics
  • Mastitis, Bovine (metabolism)
  • Milk (metabolism)
  • Penicillanic Acid (metabolism)
  • Penicillin Resistance
  • Penicillins (metabolism)
  • Pseudomonas (drug effects)
  • Species Specificity
  • Ticarcillin (metabolism)

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