Document Type

Article

Original Publication Date

1985

Journal/Book/Conference Title

Antimicrobial Agents and Chemotherapy

Volume

27

DOI of Original Publication

10.1128/AAC.27.4.487

Comments

Originally published at http://dx.doi.org/10.1128/AAC.27.4.487

Date of Submission

October 2014

Abstract

The pharmacokinetics and protein binding of ceforanide were studied in 15 patients undergoing cholecystectomies. Each patient received ceforanide (20 mg/kg) intravenously on arrival in the operating room, after which serial blood samples were collected during the elimination phase for determination of total and free ceforanide concentrations in the serum. A high-pressure liquid chromatography assay was used, with a centrifugal filtration system for free-drug determinations. Serum concentration data for each individual were subjected to linear regression to determine the elimination rate constants (total and free drug), volumes of distribution, and systemic clearances. The mean elimination rate constants were 0.41 and 0.50 h-1 for total and free ceforanide, respectively. The mean percentage of ceforanide bound to serum protein was 87.9%. The relationship of the free ceforanide concentration to the total concentration appeared to be linear. The data were fit to double-reciprocal and half-reciprocal relationships with good agreement, showing one binding site and an association constant range of 1.6 X 10(7) to 1.9 X 10(7) at these in vivo concentrations. The mean volume of distribution and mean systemic clearance of total drug were 100 ml/kg and 45.9 ml/min per 1.73 m2, respectively. Ceforanide consistently produced higherintraoperative total drug concentrations compared with those of cefazolin and cefoxitin from similar studies.

Rights

© 1985, American Society for Microbiology

Is Part Of

Publications from the Office of the Dean of the VCU School of Pharmacy

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