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A clinical evaluation of the pharmacokinetics and pharmacodynamics of intravenous alfaxalone in cyclodextrin in male and female rats following a loading dose and constant rate infusion

机译:负荷剂量和恒速输注后雄性和雌性大鼠中静脉注射紫杉醇在环糊精中的药代动力学和药效学的临床评价

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摘要

Objective: To characterise, as a clinical study, the pharmacokinetics and pharmacodynamics and describe the hypnotic effect of the neurosteroid alfaxalone (3α-hydroxy-5 α-pregnane-11, 20-dione) formulated with 2-hydroxypropyl-β-cyclodextrin in male and female rats.\udStudy design: Prospective, experimental laboratory study.\udAnimals: Twelve (six male and six female) adult, aged matched Sprague Dawley rats.\udMethods: Surgery and instrumentation was performed under isoflurane anaesthesia in an oxygen/nitrous oxide mixture (1:2) and local anaesthetic infiltration. All animals received a loading dose (1.67 mg kg -1 minute -1) for 2.5 minutes followed by a constant rate infusion (0.75 mg kg -1 minute -1) for 120 minutes of alfaxalone. Isoflurane and nitrous oxide was discontinued 2.5 minutes after the alfaxalone infusion started. Cardiorespiratory variables (heart rate, respiratory rate, arterial blood pressure, end tidal carbon dioxide tension) and clinical signs of anaesthetic depth were evaluated throughout anaesthesia. Carotid artery blood samples were collected at strategic time points for blood gas analysis, haematology and biochemistry and plasma concentrations of alfaxalone. Plasma samples were assayed using liquid chromatography-mass spectrometry (LC/MS).\udResults: There were significant differences between the sexes for plasma clearance (p = 0.0008), half-life (p = 0.0268) and mean residence time (p = 0.027). Mean arterial blood pressure was significantly higher in the male rats (p = 0.0255).\udConclusions and clinical relevance: This study confirms alfaxalone solubilized in a 2-hydroxypropyl-β-cyclodextrin provides excellent total intravenous anaesthesia in rats. Sex-based differences in pharmacokinetics and pharmacodynamics were demonstrated and must be considered when designing biomedical research models using alfaxalone.
机译:目的:以临床研究为特征,用2-羟丙基-β-环糊精配制的神经甾体依法沙酮(3α-羟基-5α-孕烷-11,20-二酮)的药代动力学和药效学对男性的催眠作用\ ud研究设计:前瞻性实验研究。\\ ud动物:十二只(六只雄性和六只雌性)成年大龄成年Sprague Dawley配对大鼠。混合物(1:2)和局部麻醉药浸润。所有动物接受负荷剂量(1.67 mg kg -1分钟-1)持续2.5分钟,然后以恒定速率输注(0.75 mg kg -1分钟-1)持续120分钟的阿法沙酮。异氟烷和一氧化二氮在开始注入阿尔法沙酮后2.5分钟终止。在整个麻醉过程中,评估了心脏呼吸变量(心率,呼吸频率,动脉血压,潮气末二氧化碳张力)和麻醉深度的临床体征。在关键时间点收集颈动脉血样,以进行血气分析,血液学和生物化学以及紫杉醇的血浆浓度。结果:两性之间的血浆清除率(p = 0.0008),半衰期(p = 0.0268)和平均停留时间(p = 0.027)。雄性大鼠的平均动脉压显着升高(p = 0.0255)。结论和临床相关性:这项研究证实,溶解在2-羟丙基-β-环糊精中的阿法沙酮可以为大鼠提供出色的全静脉麻醉。已经证明了基于性别的药代动力学和药效学差异,并且在使用阿法沙酮设计生物医学研究模型时必须考虑这些差异。

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