首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous determination of an active metabolite and open-ring metabolites by high performance liquid chromatography and pharmacokinetic studies of a penem antibiotic, FCE22891, in dogs.
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Simultaneous determination of an active metabolite and open-ring metabolites by high performance liquid chromatography and pharmacokinetic studies of a penem antibiotic, FCE22891, in dogs.

机译:通过高效液相色谱法和狗中一种Penem抗生素FCE22891的药代动力学研究,同时测定活性代谢物和开环代谢物。

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摘要

A sensitive high performance liquid chromatographic method for the simultaneous determination of an active metabolite (FCE22101) and open-ring metabolites (P1, P2) of a penem antibiotic, FCE22891, in dog plasma was developed. Plasma samples were pretreated only by ultrafiltration for the determination of the metabolites. The filtrates were directly analyzed by a reversed-phase high-performance liquid chromatographic system using a two-sided bracketing injection technique. The quantitation limits of FCE22101, P1 and P2 were 0.03, 0.1 and 0.15 microgram ml-1, respectively. Analysis of the spiked plasma samples demonstrated the good accuracy and precision of the method. The proposed method was applied to the pharmacokinetic studies of an active metabolite and open-ring metabolites after oral administration of a penem antibiotic, FCE22891, in dogs. In addition, the plasma levels of unchanged FCE22891 and the possible changes of formaldehyde and acyl-L-carnitine levels in plasma, which will be generated from the ester group of FCE22891, were also investigated.
机译:建立了一种灵敏的高效液相色谱方法,用于同时测定狗血浆中青霉素抗生素FCE22891的活性代谢物(FCE22101)和开环代谢物(P1,P2)。仅通过超滤对血浆样品进行预处理以测定代谢物。滤液通过反相高效液相色谱系统,使用两面括号注入技术直接分析。 FCE22101,P1和P2的定量限分别为0.03、0.1和0.15微克ml-1。对加标血浆样品的分析证明了该方法的良好准确性和精密度。拟议的方法应用于狗口服青霉素抗生素FCE22891后的活性代谢物和开环代谢物的药代动力学研究。另外,还研究了血浆中未改变的FCE22891的水平以及血浆中甲醛和酰基L-肉碱的可能变化,这些变化将由FCE22891的酯基产生。

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