Pharmacokinetics of Remimazolam Versus Midazolam After Intravenous Administration to Horses.

IF 1.7 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY
Masafumi Kawashima, Taisuke Kuroda, Yohei Minamijima, Yosuke Yamazaki, Hiroshi Mita, Motoi Nomura, Minoru Ohta
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引用次数: 0

Abstract

Remimazolam (RMZ) is a new short-half-life benzodiazepine used in humans. We compared the pharmacokinetics and sedative effects of RMZ with those of midazolam (MDZ) in Thoroughbred horses. Six Thoroughbreds received a single IV dose of RMZ 0.05 mg/kg or MDZ 0.05 mg/kg in a randomized crossover design. Blood samples were collected, and plasma RMZ and MDZ concentrations were measured by LC-MS/MS. Plasma concentrations were analyzed by using non-compartmental analysis and a nonlinear mixed effect model. The half-life of RMZ (0.77 ± 0.15 h) was significantly shorter than that of MDZ (3.7 ± 0.3 h). The bootstrap estimates of the parameters (mean ± SD) for RMZ and MDZ were 14.0 ± 1.1 L/kg/h and 0.45 ± 0.02 L/kg/h for clearance; 2.01 ± 0.26 L/kg and 1.31 ± 0.10 L/kg for the distribution volume of steady state. RMZ clearance was significantly higher than MDZ clearance in a comparison of post hoc values for the six horses. Wobble, observed as muscle relaxation/ataxia and a diminished stimulus response to RMZ, was observed from immediately after administration until 5 min later; the response generally disappeared after 10 min. Clinical trials will determine the place of RMZ in total intravenous anesthesia for rapid and smooth recovery in horses.

静脉给药雷马唑仑与咪达唑仑的药代动力学。
雷咪唑仑(Remimazolam, RMZ)是一种新型的短半衰期苯二氮卓类药物。我们比较了RMZ与咪达唑仑(MDZ)在纯种马体内的药代动力学和镇静作用。在随机交叉设计中,6只纯种马接受单次静脉注射rmz0.05 mg/kg或mdz0.05 mg/kg。采集血样,采用LC-MS/MS法测定血浆RMZ和MDZ浓度。血浆浓度分析采用非区室分析和非线性混合效应模型。RMZ的半衰期(0.77±0.15 h)明显短于MDZ(3.7±0.3 h)。RMZ和MDZ参数的自举估计(mean±SD)为14.0±1.1 L/kg/h,间隙为0.45±0.02 L/kg/h;稳态分布容积为2.01±0.26 L/kg, 1.31±0.10 L/kg。六匹马的RMZ清除率明显高于MDZ清除率。从给药后立即到5分钟后,观察到肌肉松弛/共济失调和RMZ刺激反应减弱的摇摆;反应一般在10分钟后消失。临床试验将确定RMZ在全静脉麻醉中的位置,以使马快速平稳恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.10
自引率
15.40%
发文量
69
审稿时长
8-16 weeks
期刊介绍: The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.
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