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Pharmacokinetics of oral cefcanel daloxate hydrochloride in healthy volunteers and patients with various degrees of impaired renal function.

Abstract
Cefcanel daloxate hydrochloride is a new oral cephalosporin prodrug. It is a double cephem ester of cefcanel, which is the active principle released in the body after uptake of an intermediate cephem mono ester. The present study investigated the pharmacokinetics of cefcanel following a single oral dose of cefcanel daloxate hydrochloride 300 mg to healthy volunteers and to patients with various degrees of stable renal insufficiency. Twenty individuals from 21 to 74 years of age received a single oral dose of cefcanel daloxate hydrochloride together with an i.v. bolus injection of iohexol for a simultaneous assessment of glomerular filtration rate (GFR). The concentrations of cefcanel and iohexol in plasma and urine were measured using high performance liquid chromatography. Cefcanel renal clearance and fraction excreted in the urine were linearly correlated with renal function and thus, logarithmic increases in plasma area under the concentration versus time curve and plasma elimination half-life were seen with decreasing GFR. Although steady state kinetics were not performed our findings suggest that a dosage reduction is not necessary even in pre-uraemic patients.
AuthorsB Edwall, L Slettevold, E Thurmann-Nielsen, R Walstad, A Torrång, K Dahl
JournalThe Journal of antimicrobial chemotherapy (J Antimicrob Chemother) Vol. 33 Issue 2 Pg. 281-8 (Feb 1994) ISSN: 0305-7453 [Print] England
PMID8182009 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Cephalosporins
  • Prodrugs
  • Iohexol
  • cefcanel daloxate
Topics
  • Administration, Oral
  • Adult
  • Aged
  • Cephalosporins (administration & dosage, pharmacokinetics)
  • Chromatography, High Pressure Liquid
  • Female
  • Glomerular Filtration Rate
  • Half-Life
  • Humans
  • Iohexol (metabolism)
  • Male
  • Metabolic Clearance Rate
  • Middle Aged
  • Prodrugs (administration & dosage, pharmacokinetics)
  • Renal Insufficiency (metabolism)

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