Plasma and faecal disposition kinetic of moxidectin after oral admnistration in horses.

Citation
R. Perez et al., Plasma and faecal disposition kinetic of moxidectin after oral admnistration in horses., ARCH MED V, 33(1), 2001, pp. 77-88
Citations number
29
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
ARCHIVOS DE MEDICINA VETERINARIA
ISSN journal
0301732X → ACNP
Volume
33
Issue
1
Year of publication
2001
Pages
77 - 88
Database
ISI
SICI code
0301-732X(2001)33:1<77:PAFDKO>2.0.ZU;2-O
Abstract
A study was undertaken with the aim to study the plasma disposition kinetic and the faecal excretion profile of moxidectin after oral administration i n horses. Five mixedbred saddle horses of 416.8 +/- 49.5 kg body weight and positives to the nematodes faecal eggs count were treated with an oral gel formulation of moxidectin (Equest((R))) at doses of 0.4 mg/kg. Blood and f aecal samples were collected before and at different rimes after treatment for a period of 75 days. After solid phase extraction and derivatization sa mples were analysed by high performance liquid chromatography (HPLC). Data were analysed by a computerised kinetic analysis. The limit of quantification of the method was 0.5 ng/mL and the drug was de tected in the plasma between 30 min (33.9 +/- 17.8 ng/mL) to 75 days post a dministration (0.3 +/- 0.2 ng/mL). The analysis of pharmacokinetic paramete rs showed a short half life of absorption ( t _ ab 0.84 +/- 0.5 h) and valu es of maximum concentration (Cmax) of 68.7 +/- 24.1 ng/mL obtained at 0.117 +/- 0.07 d (Tmax). The terminal half life of elimination (t _beta) was 18. 3 +/- 3,2 d, which produces a delayed mean residence time (MRT of 19.6 +/- 4.6 d). The area under the concentration time curve was: 172.3 +/- 51.2 ng. d / mt. The mean concentration of moxidectin in faeces ranged between 423.5 +/- 570.7 ng/g at 24 h and 0.8 +/- 0.8 ng/g 75 d after treatment. The mean maximum faecal concentration (Cmax) 5204.5 +/- 916.5 ng/g was observed at 2.5 d post-treatment. It is concluded that moxidectin has a delayed period of permanency in the organism when it is administered by oral route in hors es.