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Pharmacokinetics and pharmacodynamics of a therapeutic dose of unfractionated heparin (200 U/kg) administered subcutaneously or intravenously to healthy dogs

机译:对健康犬皮下或静脉内给予治疗剂量的普通肝素(200 U / kg)的药代动力学和药效学

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摘要

Objectives: To evaluate the effects of 200 U/kg of sodium unfractionated heparin (UFH) on coagulation times in dogs after IV and SC administration and to compare these effects with plasma heparin concentrations assessed by its anti Xa activity. Methods: 200 U/kg of UFH were administered Intravenously (IV) and Subcutaneously (SC) to five healthy adult Beagle dogs with a wash out period of at least 3 days. Activated Partial Thromboplastin Time (APTT), Prothrombin Time (PT) and plasma anti-factor Xa (aXa) activity were determined in serial blood samples. Results: After IV injection, PT remained unchanged except for a slight increase in one dog; APTT was not measurable (> 60 s) for 45 to 90 min, then decreased regularly and returned to baseline values between 150 and 240 min. High plasma heparin concentrations were observed (C max = 4.64±1.4 aXa U/mL) and decreased according to a slightly concave-convex pattern on a semi-logarithmic curve but returned to baseline slightly more slowly (t240 to t300 min). After SC administration, APTT was moderately prolonged (mean±SD prolongation: 1.55±0.28 x APTT t0, range [1.35-2.01]) between 1 and 4 hours after administration. Plasma anti-factor Xa activity reached a maximum of 0.56±0.20 aXa U/mL, range: [0.42 - 0.9] after 132±26.8 min and this lasted for 102±26.8 min. Heparin concentrations were grossly correlated to APTT; prolongation of APTT of 120 to 160% corresponded to plasma heparin concentrations range of 0.3-0.7 aXa U/mL, considered as the therapeutic range in human medicine. Conclusions: As in human, pharmacokinetic of UFH in dogs is non linear. Administration of 200 U/kg of UFH SC in healthy dogs results in sustained plasma heparin concentrations in accordance with human recommendations for thrombosis treatment or prevention, without excessively increased bleeding risks. In these conditions, APTT can be used as a surrogate to assess plasma heparin concentrations. This has to be confirmed in diseased animals.
机译:目的:评估200 U / kg普通肝素钠(UFH)对IV和SC给药后狗的凝血时间的影响,并将这些影响与通过其抗Xa活性评估的血浆肝素浓度进行比较。方法:对五只健康的成年Beagle犬进行静脉(IV)和皮下(SC)施用200 U / kg UFH,冲洗时间至少为3天。在连续血样中测定了活化的部分凝血活酶时间(APTT),凝血酶原时间(PT)和血浆抗因子Xa(aXa)活性。结果:静脉注射后,PT保持不变,只是一只狗略有增加。 APTT在45至90分钟内无法测量(> 60 s),然后有规律地降低,并在150至240分钟之间恢复到基线值。观察到较高的血浆肝素浓度(C max = 4.64±1.4 aXa U / mL),并根据半对数曲线上的略微凹凸曲线的模式降低,但恢复到基线的速度稍慢(t240至t300 min)。 SC给药后,APTT在给药后1到4小时内有中等程度的延长(平均值±SD延长:1.55±0.28 x APTT t0,范围[1.35-2.01])。血浆抗因子Xa活性在132±26.8分钟后最高达到0.56±0.20 aXa U / mL,范围为[0.42-0.9],持续时间为102±26.8分钟。肝素浓度与APTT密切相关; APTT延长120至160%相当于血浆肝素浓度范围为0.3-0.7 aXa U / mL,被认为是人类医学的治疗范围。结论:与人类一样,狗中UFH的药代动力学是非线性的。在健康犬中给予200 U / kg UFH SC可使血浆中的肝素浓度持续升高,符合人类对血栓形成或预防的建议,而不会过度增加出血风险。在这些情况下,APTT可用作评估血浆肝素浓度的替代物。必须在患病动物中证实这一点。

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