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给犊牛注射两种新霉素B制剂后的药代动力学变量比较。

Comparison of pharmacokinetic variables for two injectable formulations of netobimin administered to calves.

作者信息

Lanusse C E, Ranjan S, Prichard R K

机构信息

Institute of Parasitology of McGill University, Macdonald College, Ste-Anne de Bellevue, Quebec, Canada.

出版信息

Am J Vet Res. 1990 Sep;51(9):1459-63.

PMID:2396793
Abstract

In a 4 x 4 crossover-design study, pharmacokinetic variables of 2 injectable formulations of netobimin (trisamine salt solution and zwitterion suspension) were compared after SC administration in calves at dosage of 12.5 mg/kg of body weight. Netobimin parent drug was rapidly absorbed, being detected between 0.25 and 12 hours after treatment, with maximal plasma drug concentration (Cmax) values of 2.20 +/- 1.03 micrograms/ml achieved at 0.75 +/- 0.19 hour (trisamine) and 1.37 +/- 0.59 micrograms/ml at 0.81 +/- 0.18 hour (zwitterion). Netobimin area under the plasma concentration-time curve (AUC) was 7.59 +/- 3.11 micrograms.h/ml (trisamine) and 6.98 +/- 1.60 micrograms.h/ml (zwitterion). Elimination half-life (t1/2 beta) was 2.59 +/- 0.63 hours (trisamine) and 3.57 +/- 1.45 hours (zwitterion). Albendazole was not detected at any time. Albendazole sulfoxide was detected from 4 hours up to 20 hours (trisamine) and from 6 hours up to 24 hours (zwitterion) after administration of the drug. The Cmax values were 0.48 +/- 0.16 micrograms/ml and 0.46 +/- 0.26 micrograms/ml for trisamine and zwitterion formulations, respectively, achieved at time to peak drug concentration (Tmax) values of 9.50 +/- 1.41 hours (trisamine) and 11.30 +/- 1.04 hours (zwitterion). Albendazole sulfoxide AUC was 3.86 +/- 1.04 micrograms.h/ml (trisamine) and 4.40 +/- 3.24 micrograms.h/ml (zwitterion); t1/2 beta was 3.05 +/- 0.75 hours (trisamine) and 3.90 +/- 1.44 hours (zwitterion). Albendazole sulfone was detected from 4 (trisamine) or 6 hours (zwitterion) to 24 hours after treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项4×4交叉设计研究中,比较了两种注射用硝碘酚腈制剂(三胺盐溶液和两性离子悬浮液)在犊牛体内以12.5mg/kg体重皮下给药后的药代动力学变量。硝碘酚腈母体药物吸收迅速,给药后0.25至12小时可检测到,三胺盐制剂在0.75±0.19小时达到最大血浆药物浓度(Cmax)值为2.20±1.03μg/ml,两性离子悬浮液在0.81±0.18小时达到1.37±0.59μg/ml。硝碘酚腈的血浆浓度-时间曲线下面积(AUC)为7.59±3.11μg·h/ml(三胺盐)和6.98±1.60μg·h/ml(两性离子)。消除半衰期(t1/2β)为2.59±0.63小时(三胺盐)和3.57±1.45小时(两性离子)。任何时间均未检测到阿苯达唑。给药后,在4至20小时(三胺盐)和6至24小时(两性离子)检测到阿苯达唑亚砜。三胺盐制剂和两性离子悬浮液的Cmax值分别为0.48±0.16μg/ml和0.46±0.26μg/ml,分别在达峰时间(Tmax)为9.50±1.41小时(三胺盐)和11.30±1.04小时(两性离子)时达到。阿苯达唑亚砜的AUC为3.86±1.04μg·h/ml(三胺盐)和4.40±3.24μg·h/ml(两性离子);t1/2β为3.05±0.75小时(三胺盐)和3.90±1.44小时(两性离子)。给药后4小时(三胺盐)或6小时(两性离子)至24小时检测到阿苯达唑砜。(摘要截短于250字)

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