Errecalde J O, Lanusse C E, Landoni M F
Cátedra de Farmacología, Facultad de Ciencias Veterinarias, Universidad Nacional de La Plata, Argentina.
Zentralbl Veterinarmed A. 1990 Apr;37(3):163-9. doi: 10.1111/j.1439-0442.1990.tb00890.x.
The pharmacokinetics and bioavailability of neomycin in sheep were investigated following intravenous, intramuscular, subcutaneous and intratracheal administration of 10 mg/kg. A rapid distribution phase (t 1/2 alpha, 3.16 min) was followed by a slower elimination phase (t1/2 beta, 1.98 h). The apparent volume of distribution was 304.69 ml/kg. Absorption half-lives were 18.62, 21.22 and 40.83 min and elimination half-lives 2.68, 2.82 and 2.55 h after IM, SC and IT administration, respectively. Bioavailabilities between 0.74 and 0.85 were obtained for the three routes of administration. Based on the bioavailability and disposition kinetics of neomycin, a twice daily IM dosage regimen should both be practical and adequate to maintain plasma neomycin concentrations within the pharmacologically active but nontoxic range.
在绵羊中静脉注射、肌肉注射、皮下注射和气管内注射10mg/kg新霉素后,对其药代动力学和生物利用度进行了研究。快速分布相(t1/2α,3.16分钟)之后是较慢的消除相(t1/2β,1.98小时)。表观分布容积为304.69ml/kg。肌肉注射、皮下注射和气管内注射后的吸收半衰期分别为18.62、21.22和40.83分钟,消除半衰期分别为2.68、2.82和2.55小时。三种给药途径的生物利用度在0.74至0.85之间。基于新霉素的生物利用度和处置动力学,每日两次的肌肉注射给药方案既实用又足以将血浆新霉素浓度维持在药理活性但无毒的范围内。