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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 >Validated LC-MS/MS assay for quantitative determination of deoxypodophyllotoxin in rat plasma and its application in pharmacokinetic study
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Validated LC-MS/MS assay for quantitative determination of deoxypodophyllotoxin in rat plasma and its application in pharmacokinetic study

机译:用于定量测定大鼠血浆中脱氧氧基毒素的定量测定的验证的LC-MS / MS测定及其在药代动力学研究中的应用

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摘要

A rapid and sensitive liquid chromatography/tandem mass spectrometry method was developed and validated for the quantification of deoxypodophyllotoxin (DPT) concentration in rat plasma with diazepam as internal standard (IS). DPT and IS were extracted with ethyl acetate, and the chromatographic separation was accomplished by using a Waters Symmetry C18 analytical column (2.1mm×150mm, 5μm) with a mobile phase consisting of acetonitrile and deionized water (70:30, v:v) containing 0.1% formic acid at a flow rate of 0.2mL/min. Multiple Reaction Monitoring (MRM), using electrospray ionization in positive ion mode, was employed to quantitatively detect DPT and IS. The monitored transitions were set at m/z 399.05-231.00 and m/z 285.00-154.00 for DPT and IS, respectively. The calibration curve was linear over the concentration range of 7.8-1000ng/mL (R2≥0.9999). The intra- and inter-day precision values were less than 7%. Similarly, the mean intra- and inter-day accuracy were found to be within -2.8% to 1.9% of the interval, with all samples locating within general assay acceptability criteria for QC samples according to FDA guidelines. This method was further and successfully applied in the pharmacokinetics study of DPT in rat.
机译:开发了一种快速敏感的液相色谱/串联质谱法,并验证了大鼠等离子体中的脱氧氧基毒素(DPT)浓度,用DiazePAM作为内标(是)。 DPT和用乙酸乙酯萃取,通过使用由乙腈和去离子水的流动相(70:30,V:V)组成的流动相,通过使用水域对称C18分析柱(2.1mm×150mm,5μm)来完成色谱分离。以0.2ml / min的流速含有0.1%的甲酸。使用在正离子模式下使用电喷雾电离的多反应监测(MRM)来定量检测DPT。监控的过渡设置为M / Z 399.05-231.00和M / Z 285.00-154.00,分别为DPT,并且分别为M / Z 285.00-154.00。校准曲线在7.8-1000ng / ml的浓度范围内是线性的(R2≥0.9999)。内部和日间精密值小于7%。同样,发现平均值和日间准确度在间隔中的-2.8%至1.9%内,所有样品都在普通测定中定位的QC样品的可接受性标准,根据FDA指南。进一步且成功地应用于大鼠DPT的药代动力学研究。

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