Lanusse C E, Prichard R K
Institute of Parasitology, McGill University, Macdonald College, Quebec, Canada.
J Vet Pharmacol Ther. 1990 Jun;13(2):170-8. doi: 10.1111/j.1365-2885.1990.tb00765.x.
The pharmacokinetics and the profile of urine excretion of netobimin (NTB) and its metabolites were investigated after its intraruminal (i.r.) and subcutaneous (s.c.) administration to sheep at 20 mg/kg. Plasma and urine concentrations of NTB, albendazole (ABZ), albendazole sulphoxide (ABZSO) and albendazole sulphone (ABZSO2) were measured serially over a 120-h period by HPLC. NTB showed a similar pharmacokinetic profile in both treatments, being detected between 0.5 and 12 h post-treatment, but the tmax was achieved significantly earlier (P less than 0.05) after s.c. treatment. ABZ was detected in plasma only after i.r. treatment, resulting in a low area under the curve (AUC). The peak plasma concentration (Cmax) and AUC for ABZSO and ABZSO2 were significantly higher after i.r. administration of NTB. In both treatments, the ABZSO Cmax was reached earlier than the ABZSO2 Cmax. The ratio of AUC ABZSO2:ABZSO was higher following s.c. administration (1.33) than following i.r. administration (0.35). The percentages of total dose excreted in the urine as NTB, ABZ, ABZSO and ABZSO2 were 17.05 (i.r.) and 8.16 (s.c.). There was a less efficient conversion of NTB into ABZ metabolites after s.c. administration. The detection of ABZ in plasma and the high ABZSO AUC obtained after i.r. treatment may be of major importance for anthelmintic efficacy.
将20mg/kg的奈托比明(NTB)分别经瘤胃内(i.r.)和皮下(s.c.)给药于绵羊后,研究了其药代动力学以及NTB及其代谢产物的尿排泄情况。在120小时内,通过高效液相色谱法(HPLC)连续测定血浆和尿液中NTB、阿苯达唑(ABZ)、阿苯达唑亚砜(ABZSO)和阿苯达唑砜(ABZSO2)的浓度。两种给药方式下NTB的药代动力学特征相似,给药后0.5至12小时可检测到,但皮下给药后达峰时间显著更早(P小于0.05)。仅在瘤胃内给药后血浆中检测到ABZ,导致其曲线下面积(AUC)较低。瘤胃内给药NTB后,ABZSO和ABZSO2的血浆峰浓度(Cmax)和AUC显著更高。两种给药方式下,ABZSO的Cmax均早于ABZSO2的Cmax。皮下给药后ABZSO2与ABZSO的AUC比值(1.33)高于瘤胃内给药(0.35)。以NTB、ABZ、ABZSO和ABZSO2形式经尿液排泄的总剂量百分比分别为17.05(瘤胃内给药)和8.16(皮下给药)。皮下给药后NTB转化为ABZ代谢产物的效率较低。瘤胃内给药后血浆中ABZ的检测以及较高的ABZSO AUC可能对驱虫效果至关重要。