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高效液相色谱法测定马血浆中的非甾体抗炎药(如菲诺昔康)。

Determination of firocoxib in equine plasma using high performance liquid chromatography.

机构信息

University of Tennessee, Department of Comparative Medicine, College of Veterinary Medicine, 2407 River Drive, Knoxville, TN 37996, USA.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jan 15;879(2):205-8. doi: 10.1016/j.jchromb.2010.11.026. Epub 2010 Dec 3.

Abstract

A new method of analysis has been developed and validated for the determination of firocoxib, a new nonsteroidal anti-inflammatory drug (NSAID) approved for use in horses and dogs to control pain and inflammation associated with osteoarthritis. Following a liquid extraction using ethyl acetate:hexane (40:60), samples were separated by isocratic reversed-phase HPLC on a Sunfire C(18) column and quantified using UV detection at 290 nm. The mobile phase was a mixture of water with 0.025% trifluoroacetic acid and acetonitrile, with a flow-rate of 1.1 ml/min. The procedure produced a linear curve over the concentration range 5-1500 ng/ml with a lower limit of quantification of 5 ng/ml. Intra- and inter-assay variability was less than 7%. The average recovery was 98%. The method is suitable for the analysis of clinical samples from pharmacokinetic studies and can also be used for small volume sample sizes.

摘要

已开发并验证了一种新的分析方法,用于测定非甾体抗炎药(NSAID)昔布考昔的含量。昔布考昔是一种新型药物,已获准用于马和犬,用于控制与骨关节炎相关的疼痛和炎症。样品经乙酸乙酯:正己烷(40:60)液液萃取后,采用 Sunfire C(18)柱进行等度反相高效液相色谱分离,并在 290nm 处进行紫外检测定量。流动相为含 0.025%三氟乙酸的水和乙腈的混合物,流速为 1.1ml/min。该方法在 5-1500ng/ml 的浓度范围内呈线性曲线,定量下限为 5ng/ml。日内和日间变异性均小于 7%。平均回收率为 98%。该方法适用于药代动力学研究中临床样品的分析,也可用于小体积样品的分析。

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