Pharmacokinetics of Enrofloxacin After Intravenous and Intramuscular Administration in Angora Goats

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Küçük Resim

Tarih

2001

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

CANADIAN VET MED ASSOC

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

Pharmacokinetics and bioavailability of enrofloxacin were determined after single intravenous (IV) and intramuscular (IM) administrations of 5 mg/kg body weight (BW) to 5 healthy adult Angora goats. Plasma enrofloxacin concentrations were measured by high performance liquid chromatography. Pharmacokinetics were best described by a 2-compartment open model. The elimination half-life and volume of distribution after IV and IM administrations were similar (t(1/2 beta), 4.0 to 4.7 h and V-d(ss),1.2 to 1.5 L/kg, respectively). Enrofloxacin was rapidly (t(1/2a), 0.25 h) and almost completely absorbed (F, 90%) after IM administration. Mean plasma concentrations of enrofloxacin at 24 h after IV and IM administration (0.07 and 0.09 mug/mL, respectively) were higher than the minimal inhibitory concentration (MIC) values for most pathogens. In conclusion, once-daily IV and IM administration of enrofloxacin (5 mg/kg BW) in Angora goats may be useful in treatment of infectious diseases caused by sensitive pathogens.

La phairmacocinL3tiq1e et /a biodispoiiibilite de /'enirofloxaciniefuirenit determintees sluite n liune adminiistrationi uniiiqlue par voic inztraveinielise (IV) on intramuiiiscldaire (IM) diu niedicamen t d lone dose de 5 mtg/kg de poids corporel (p.c.) d cinq chevres Angora adl iltes en sanWt. Les concentrationis plasmlatiques d'enrofloxacinefitrent miesurees par chroniatographie de hallte performance en phase liquide. Un mlodde oilvert d deuix compartimnents decrit le mieux /a pharmacocinttiqule de /'enrofloxacinie. La demni-vie d'limibinationi et le vol/nie de distriblution apres administrationi IV olu IM etaient sim ilaires et respectivenment de t ,1),, 4,0-4,7 h et Va,, 1,2-1,5 L/kg. L'enrofloxacintefit rapidemtent (t 11,71, 0,25 h) et presqlue coam plktenient (F, 90 %) absorbee apres adnministrationt IM. Les concentrations plasniatiquies moyennes d'enrofloxacine 24 hi apres admiinistrationi IV et IM etaient respectivement de 0,07 et 0,09 Lg/niL et etaient plus levees quie /a concentrationi niinimale inihibitrice de /a pll/part des mlicro-organ ismes pathogenes. En conclusioni, itnie admiinistration qluotidienne par voie IV otl IM d'enrofloxacinie n la dose de 5 mug/kg p.c. c/iez des chevres Angora polurrait s'averer lutile polur le traitemlent de nialadies infectielnses canisLes par des bacteries pat hogMnes sensibles.

Açıklama

Anahtar Kelimeler

Kaynak

Canadian Journal of Veterinary Research-revue Canadienne De Recherche Veterinaire

WoS Q Değeri

N/A

Scopus Q Değeri

Q2

Cilt

65

Sayı

1

Künye

Elmas, M., Traş, B., Kaya, S., Baş, A. L., Yazar, E., Yarsan, E., (2001). Pharmacokinetics of Enrofloxacin After Intravenous and Intramuscular Administration in Angora Goats. Canadian Journal of Veterinary Research-revue Canadienne De Recherche Veterinaire, 65(1), 64-67.