Absorption and Distribution of Toltrazuril and Toltrazuril Sulfone in Plasma, Intestinal Tissues and Content of Piglets after Oral or Intramuscular Administration
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
PubMed
34577103
PubMed Central
PMC8468611
DOI
10.3390/molecules26185633
PII: molecules26185633
Knihovny.cz E-zdroje
- Klíčová slova
- Isospora suis, anticoccidials, coccidiosis, pharmacokinetics, prevention, swine, tissue distribution,
- MeSH
- aplikace orální MeSH
- ileum metabolismus MeSH
- injekce intramuskulární MeSH
- jejunum metabolismus MeSH
- kokcidiostatika aplikace a dávkování metabolismus farmakokinetika MeSH
- kokcidióza prevence a kontrola veterinární MeSH
- nemoci prasat prevence a kontrola MeSH
- prasata MeSH
- střevní sliznice metabolismus MeSH
- sulfony aplikace a dávkování metabolismus farmakokinetika MeSH
- tělesná hmotnost účinky léků MeSH
- triaziny aplikace a dávkování metabolismus farmakokinetika MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- kokcidiostatika MeSH
- sulfony MeSH
- toltrazuril MeSH Prohlížeč
- triaziny MeSH
Piglet coccidiosis due to Cystoisospora suis is a major cause of diarrhea and poor growth worldwide. It can effectively be controlled by application of toltrazuril (TZ), and oral formulations have been licensed for many years. Recently, the first parenteral formulation containing TZ in combination with iron (gleptoferron) was registered in the EU for the prevention of coccidiosis and iron deficiency anemia, conditions in suckling piglets requiring routine preventive measures. This study evaluated the absorption and distribution of TZ and its main metabolite, toltrazuril sulfone (TZ-SO2), in blood and intestinal tissues after single oral (20 mg/kg) or single intramuscular (45 mg/piglet) application of TZ. Fifty-six piglets were randomly allocated to the two treatment groups. Animals were sacrificed 1-, 5-, 13-, and 24-days post-treatment and TZ and TZ-SO2 levels were determined in blood, jejunal tissue, ileal tissue, and mixed jejunal and ileal content (IC) by high performance liquid chromatography (HPLC). Intramuscular application resulted in significantly higher and more sustained concentrations of both compounds in plasma, intestinal tissue, and IC. Higher concentrations after oral dosing were only observed one day after application of TZ in jejunum and IC. Toltrazuril was quickly metabolized to TZ-SO2 with maximum concentrations on day 13 for both applications. Remarkably, TZ and TZ-SO2 accumulated in the jejunum, the primary predilection site of C. suis, independently of the administration route, which is key to their antiparasitic effect.
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