Pharmacokinetics of marbofloxacin in Japanese quails (Coturnix japonica) after different routes of administration.
Journal of American Science. 2015, 11(4): 136-142. • 2015
معلومات البحث
المؤلفون
Mohamed Aboubakr and Abdelazem Mohamed Abdelazem
الكلمات المفتاحية
pharmacokinetics, quail. marbofloxacin
المجلة العلمية
Journal of American Science. 2015, 11(4): 136-142.
الناشر
Not Available
المجلد
11
العدد
4
الصفحات
136-142
publication.type
International
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
In this study the disposition kinetics and plasma availability of marbofloxacin in Japanese quails after
single intravenous (IV), intramuscular (IM) and oral (PO) administrations of 5 mg/kg BW were investigated.
Following IV injection, elimination half-life (t1/2β), mean value of distribution at steady state (Vdss), total body
clearance (Cltot) and mean residence time (MRT) of marbofloxacin were 4.03 h, 1.24 l/kg, 0.19 l/h/kg and 5.89 h,
respectively. Following IM and PO administration of marbofloxacin at the same dose, the peak plasma concentration
(Cmax) were 3.86 and 3.59 μg/ml, respectively, which was obtained at 1.58 and 1.60 h, the time to peak concentration
(tmax) for both routes. Elimination half-lives (t1/2el) were 6.70 and 6.19 h, respectively, and mean absorption time
(MAT) was 1.79 and 1.19 h, respectively. The systemic bioavailability following IM and PO administration were
98.72 and 87.94%, respectively. In vitro protein binding percent was 26.38%. Analysis of pharmacokinetic data
obtained in this study reveals that a dosage of 5 mg/kg BW given by IM or PO routes every 24 h in Japanese quails
might be recommended for a successful clinical effect in quails.
single intravenous (IV), intramuscular (IM) and oral (PO) administrations of 5 mg/kg BW were investigated.
Following IV injection, elimination half-life (t1/2β), mean value of distribution at steady state (Vdss), total body
clearance (Cltot) and mean residence time (MRT) of marbofloxacin were 4.03 h, 1.24 l/kg, 0.19 l/h/kg and 5.89 h,
respectively. Following IM and PO administration of marbofloxacin at the same dose, the peak plasma concentration
(Cmax) were 3.86 and 3.59 μg/ml, respectively, which was obtained at 1.58 and 1.60 h, the time to peak concentration
(tmax) for both routes. Elimination half-lives (t1/2el) were 6.70 and 6.19 h, respectively, and mean absorption time
(MAT) was 1.79 and 1.19 h, respectively. The systemic bioavailability following IM and PO administration were
98.72 and 87.94%, respectively. In vitro protein binding percent was 26.38%. Analysis of pharmacokinetic data
obtained in this study reveals that a dosage of 5 mg/kg BW given by IM or PO routes every 24 h in Japanese quails
might be recommended for a successful clinical effect in quails.
أعضاء هيئة التدريس - جامعة بنها