首页> 外文期刊>Research in Veterinary Science >Pharmacokinetic study of an injectable long-acting parenteral formulation of doxycycline hyclate in calves.
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Pharmacokinetic study of an injectable long-acting parenteral formulation of doxycycline hyclate in calves.

机译:小牛强力霉素盐酸盐注射剂长效肠胃外制剂的药代动力学研究。

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摘要

Doxycycline hyclate (DOX-h) can be regarded as a time-dependant antibacterial. Hence, a parenteral long-acting formulation may be regarded as more pharmacologically sound. A poloxamer-based matrix was used to produce a long-acting injectable preparation (DOX-h-LA) and its serum concentrations vs. time profile investigated after its s.c. injection to calves. Serum concentrations profiles for such a prepartion were compared to the corresponding profiles obtained with an aqueous formulation of DOX-h injected either i.m. or i.v. in 10 calves in a crossover study at dose of 10mg/kg, with washout periods. DOX-h-LA showed the greatest values for bioavailability (602%); maximum serum concentration (C(max)) value was 1.99mug/mL with a time to reach C(max) (T(max)) of 25h and an elimination half-life of 40.81h. Considering minimum effective serum concentration of 0.5mug/mL a dose-interval of 80h can be achieved for DOX-h-LA, and only 9.7h and 17h after the i.v. or i.m. administration of DOX-h, respectively.
机译:盐酸多西环素(DOX-h)可被视为一种时间依赖性抗菌剂。因此,肠胃外长效制剂可被认为在药理学上更合理。基于泊洛沙姆的基质用于制备长效可注射制剂(DOX-h-LA),并在s.c.之后研究其血清浓度与时间的关系。注射到小腿。将这样的部分的血清浓度曲线与经腹膜内注射DOX-h的水性制剂获得的相应曲线进行比较。或i.v.在10头小牛的交叉研究中,剂量为10mg / kg,并有洗脱期。 DOX-h-LA的生物利用度最高(602%);最大血清浓度(C(max))值为1.99mug / mL,达到C(max)(T(max))的时间为25h,消除半衰期为40.81h。考虑到最低有效血清浓度为0.5mug / mL,对于DOX-h-LA可以达到80h的剂量间隔,而静脉注射后仅9.7h和17h。或我分别使用DOX-h。

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