首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of vinpocetine and its primary metabolite, apovincaminic acid, in rat plasma by liquid chromatography-tandem mass spectrometry.
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Determination of vinpocetine and its primary metabolite, apovincaminic acid, in rat plasma by liquid chromatography-tandem mass spectrometry.

机译:液相色谱-串联质谱法测定大鼠血浆中的长春西汀及其主要代谢物载脂蛋白含量。

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A precise and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for simultaneous determination of vinpocetine (VP) and its primary metabolite, apovincaminic acid (AVA), in rat plasma was developed and validated. The analytes and the internal standard-dimenhydrinate were extracted from 50 microL aliquots of rat plasma via solid-liquid extraction. Chromatographic separation was achieved in a run time of 3.5 min on a C(18) column under isocratic conditions. Detection of analytes and IS was done by tandem mass spectrometry, operating in positive ion and multiple reaction monitoring (MRM) acquisition mode. The protonated precursor to product ion transitions monitored for VP, AVA and IS were m/z 351.4-->280.2, 323.2-->280.2 and 256.2-->167.3 respectively. The method was fully validated for its sensitivity, selectivity, accuracy and precision, matrix effect, stability study and dilution integrity. A linear dynamic range of 0.5-500 ng/mL for both VP and AVA was evaluated with mean correlation coefficient (r) of 0.9970 and 0.9984 respectively. The precision of the assay (RSD%) was less than 8.55% at all concentrations levels for both VP and AVA. This method was successfully applied to a pharmacokinetic study of VP in rats after intravenous (1 mg/kg) and oral (1 mg/kg) administration.
机译:建立并验证了一种精确灵敏的液相色谱-串联质谱(LC-MS / MS)方法,该方法可同时测定大鼠血浆中的长春西汀(VP)及其主要代谢产物载脂蛋白含量(AVA)。通过固液萃取从大鼠血浆的50微升等分试样中提取分析物和内标的二羟甲基海因。在等度条件下,在C(18)色谱柱上以3.5分钟的运行时间完成了色谱分离。分析物和IS的检测是通过串联质谱法完成的,该方法以阳离子和多反应监测(MRM)采集模式运行。监测到的VP,AVA和IS的质子化前体到产物离子的跃迁分别为m / z 351.4-> 280.2、323.2-> 280.2和256.2-> 167.3。该方法的灵敏度,选择性,准确性和精密度,基质效应,稳定性研究和稀释完整性均得到了充分验证。 VP和AVA的线性动态范围为0.5-500 ng / mL,平均相关系数(r)分别为0.9970和0.9984。在VP和AVA的所有浓度水平下,测定的精密度(RSD%)均小于8.55%。该方法已成功应用于静脉(1 mg / kg)和口服(1 mg / kg)给药后大鼠VP的药代动力学研究。

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