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首页> 外文期刊>Journal of Zoo and Wildlife Medicine >SINGLE AND MULTIPLE-DOSE PHARMACOKINETICS OF MELOXICAM AFTER ORAL ADMINISTRATION TO THE RABBIT (ORYCTOLAGUS CUNICULUS)
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SINGLE AND MULTIPLE-DOSE PHARMACOKINETICS OF MELOXICAM AFTER ORAL ADMINISTRATION TO THE RABBIT (ORYCTOLAGUS CUNICULUS)

机译:口服美洛昔康对兔子的单次和多次剂量药代动力学

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摘要

The nonsteroidal anti-inflammatory durg (NSAID) meloxicam is a very analgesic, and antipyretic agent used in veterinary medicine. To determine the pharmacokinetics of this NSAID in rabbits following a single dose and 10-day Period of dosing, eight clinically normal, 8-mo-old New, Zealand white rabbits (Oryctolagus cuniculus) were administered 0.2 mg/kg meloxicam p.o. daily. Pharmacokinetic analysis of the meloxicam was determined via noncompartmental analysis. After oral administration, mean +/- standard deviation values for area under the curve were 1.8 +/- 0.50 and 2.1 +/- 0.55 mu g x h/ml, and maximum plasma concentrations were 0.17 +/- 0.06 and 0.24 +/- 0.07 mu g/ml for Day 1 and Day 10, respectively. The half-life was approximately 8 hr. Administration of meloxicam at a dosage of 0.2 to 0.3 mg/kg p.o. every 24 hr is suggested. Although a higher (lose may be required for optimum effects, this would require efficacy and safety studies in this species. Meloxicam administered at 0.2 mg/kg p.o. daily for 10 day was well tolerated by the rabbits.
机译:非甾体类抗炎药(Metalxicam)是一种非常镇痛的退热剂,用于兽药。为了确定此NSAID在单剂和10天给药期后在兔子中的药代动力学,将0.2 mg / kg美洛昔康p.o给药于八只临床正常,8个月大的新西兰白兔(Oryctolagus cuniculus)。日常。美洛昔康的药代动力学分析通过非房室分析确定。口服后,曲线下面积的平均+/-标准偏差值为1.8 +/- 0.50和2.1 +/- 0.55μgxh / ml,最大血浆浓度为0.17 +/- 0.06和0.24 +/- 0.07μg第1天和第10天分别为g / ml。半衰期约为8小时。口服美洛昔康的剂量为0.2至0.3 mg / kg p.o.建议每24小时一次。尽管要获得最佳效果,可能需要更高的剂量(需要减量,但是这需要对该物种进行功效和安全性研究。)兔子每天耐受以0.2 mg / kg p.o.每天服用美洛昔康10天。

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