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首页> 外文期刊>Pharmaceutical Chemistry Journal >Method Development for Quantitative Determination of Ormustine in Biological Fluids by High Performance Liquid Chromatography with Mass-Spectrometric Detection
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Method Development for Quantitative Determination of Ormustine in Biological Fluids by High Performance Liquid Chromatography with Mass-Spectrometric Detection

机译:高效液相色谱-质谱联用法定量测定生物流体中奥莫斯汀的方法开发

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摘要

An HPLC method over a Kromasil C18 reversed-phase column with mass spectrometric detection and EtOH:NH4OAc (10:90) mobile phase was developed for quantitative determination of the antitumor drug ormustine in biological fluids. The method enabled detection of both drug isomers, possessed sufficiently high sensitivity and specificity, and was linear over a wide range. The developed method was used to study ormustine pharmacokinetics in rabbits. It was found that the pharmacokinetics of both drug isomers after i.v. injection followed a two-compartment model. The elimination half-lives of ormustine-I were (3.5 +/- 0.2) and (109.4 +/- 22.2) min for the alpha- and beta-phases, respectively; of ormustine-II, (3.6 +/- 0.2) and (79.5 +/- 21.7) min, respectively.
机译:建立了在Kromasil C18反相色谱柱上进行质谱检测和EtOH:NH4OAc(10:90)流动相的HPLC方法,用于定量测定生物流体中的抗肿瘤药物奥姆斯汀。该方法能够检测两种药物异构体,具有足够高的灵敏度和特异性,并且在宽范围内呈线性。所开发的方法用于研究兔中的奥姆斯汀的药代动力学。发现静脉内注射后两种药物异构体的药代动力学。注射遵循两室模型。奥莫斯汀-I的消除半衰期分别为α-阶段和β-阶段的(3.5 +/- 0.2)和(109.4 +/- 22.2)min;奥莫斯汀-II分别为(3.6 +/- 0.2)分钟和(79.5 +/- 21.7)分钟。

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