Literature DB >> 6464778

Pharmacokinetics and metabolism of sulphadiazine in neonatal and young pigs.

C Friis, N Gyrd-Hansen, P Nielsen, C E Olsen, F Rasmussen.   

Abstract

The pharmacokinetics of sulphadiazine was studied in newborn, 1 week, and 8 weeks old piglets after intravenous administration of 60 mg/kg. Kinetic parameters were calculated using a two compartment open model. Steady state volume of distribution averaged 0.62, 0.56, and 0.48 1/kg at birth, 1 week, and 8 weeks, respectively. Elimination half-life decreased from 455 min. at birth to 322 min. at 1 week and 157 min. at 8 weeks leading to a rise in body clearance from 0.99 to 2.20 ml/min./kg during the same age period. Urinary excretion data indicated that the increase in body clearance reflects maturational changes in both renal function and metabolic capacity. Although renal clearance increased several times more than metabolic clearance, metabolism remained the main contributor to elimination of SDZ at all ages. Metabolism of SDZ involves two important pathways - acetylation and aromatic hydroxylation; the former being well developed at birth, while the latter increased markedly during the age period studied.

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Year:  1984        PMID: 6464778     DOI: 10.1111/j.1600-0773.1984.tb01937.x

Source DB:  PubMed          Journal:  Acta Pharmacol Toxicol (Copenh)        ISSN: 0001-6683


  2 in total

1.  A comparison of some of the pharmacokinetic parameters of three commercial sulphadiazine/trimethoprim combined preparations given orally to pigs.

Authors:  N E Søli; T Framstad; E Skjerve; S Sohlberg; S A Odegaard
Journal:  Vet Res Commun       Date:  1990       Impact factor: 2.459

2.  Study of treatment of congenital Toxoplasma gondii infection in rhesus monkeys with pyrimethamine and sulfadiazine.

Authors:  E Schoondermark-van de Ven; J Galama; T Vree; W Camps; I Baars; T Eskes; J Meuwissen; W Melchers
Journal:  Antimicrob Agents Chemother       Date:  1995-01       Impact factor: 5.191

  2 in total

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