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口服给药后,雷复尼特在哺乳和断奶羔羊体内的药代动力学。

Pharmacokinetics of rafoxanide in suckling and weaned lambs following oral administration.

作者信息

Swan G E, Mülders M S

机构信息

Department of Pharmacology and Toxicology, Faculty of Veterinary Science, University of Pretoria, Onderstepoort, Republic of South Africa.

出版信息

J S Afr Vet Assoc. 1993 Jun;64(2):67-70.

PMID:8410945
Abstract

The pharmacokinetics of rafoxanide administered orally at 15 mg kg-1 were compared in suckling lambs (n = 8), aged 5-8 weeks and weaned lambs (n = 8), aged 21-22 weeks. A significant difference (p < 0.0001) in area under the curve (AUC) and maximum plasma concentrations (Cmax) were observed between the different age groups. The bioavailability, as measured by AUC and Cmax, was 2.5-3 times greater in the suckling lambs compared to the weaned lambs. No significant differences (p > 0.05) in time to maximum plasma concentrations (Tmax), distribution half-life (T1/2 alpha), elimination half-life (T1/2 beta) and mean residence time (MRT) were observed. It was concluded that the pharmacokinetic differences observed between suckling and weaned lambs may result in an increased susceptibility of suckling lambs to the toxic effects of rafoxanide. Lambs younger than 8 weeks, should preferably not be treated with rafoxanide, or the dose must be reduced.

摘要

对5至8周龄的哺乳羔羊(n = 8)和21至22周龄的断奶羔羊(n = 8)口服15 mg kg-1雷复尼特的药代动力学进行了比较。不同年龄组之间的曲线下面积(AUC)和最大血浆浓度(Cmax)存在显著差异(p < 0.0001)。与断奶羔羊相比,哺乳羔羊通过AUC和Cmax测量的生物利用度高2.5至3倍。在达到最大血浆浓度的时间(Tmax)、分布半衰期(T1/2α)、消除半衰期(T1/2β)和平均驻留时间(MRT)方面未观察到显著差异(p > 0.05)。得出的结论是,在哺乳羔羊和断奶羔羊之间观察到的药代动力学差异可能导致哺乳羔羊对雷复尼特毒性作用的易感性增加。8周龄以下的羔羊最好不要用雷复尼特治疗,或者必须降低剂量。

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