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In Vitro Adsorption and in Vivo Pharmacokinetic Interaction between Doxycycline and Frequently Used Mycotoxin Binders in Broiler Chickens

机译:强力霉素与肉鸡常用霉菌毒素结合剂的体外吸附和体内药代动力学相互作用

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摘要

Mycotoxin binders are readily mixed in feeds to prevent uptake of mycotoxins by the animal. Concerns were raised for nonspecific binding with orally administered veterinary drugs by the European Food Safety Authority in 2010. This paper describes the screening for in vitro adsorption of doxycycline-a broad-spectrum tetracycline antibiotic-to six different binders that were able to bind >75% of the doxycycline. Next, an in vivo pharmacokinetic interaction study of doxycycline with two of the binders, which demonstrated significant in vitro binding, was performed in broiler chickens using an oral bolus model. It was shown that two montmorillonite-based binders were able to lower the area under the plasma concentration-time curve of doxycycline by >60% compared to the control group. These results may indicate a possible risk for reduced efficacy of doxycycline when used concomitantly with montmorillonite-based mycotoxin binders.
机译:霉菌毒素粘合剂很容易与饲料混合,以防止动物摄取霉菌毒素。欧洲食品安全局于2010年提出了与口服兽药非特异性结合的担忧。本文描述了多西环素(一种广谱四环素抗生素)在六种能够结合> 75的结合剂上的体外吸附筛选。多西环素的百分比。接下来,使用口服推注模型在肉鸡中进行了强力霉素与两种结合剂的体内药代动力学相互作用研究,该研究证明了显着的体外结合。结果表明,与对照组相比,两种基于蒙脱石的粘合剂能够将多西环素的血浆浓度-时间曲线下的面积降低> 60%。这些结果可能表明,与基于蒙脱石的霉菌毒素粘合剂同时使用时,强力霉素的疗效可能会降低。

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