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Simultaneous determination of human plasma protein binding of bioactive flavonoids in Polygonum orientale by equilibrium dialysis combined with UPLC–MS/MS

机译:平衡透析与UPLC–MS / MS联用同时测定东方何首乌中生物活性类黄酮的人血浆蛋白结合

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摘要

A simple and selective ultra performance liquid chromatography–electrospray ionization tandem mass spectrometry (UPLC–ESI-MS/MS) assay was developed for the determination of the human plasma protein binding of four bioactive flavonoids (such as orientin and vitexin) in Polygonum orientale. Protein precipitation was used for sample preparation. Equilibrium dialysis technique was applied to determine the plasma protein binding under physiological conditions. The separation was achieved through a Waters C18 column with a mobile phase composed of 0.1% formic acid in acetonitrile and 0.1% aqueous formic acid using step gradient elution at a flow rate of 0.35 mL/min. A Waters ACQUITY™ TQD system was operated under the multiple reaction monitoring (MRM) mode of positive electrospray ionization. All of the recovery, precision, accuracy and stability of the method met the requirements. Good correlations (r>0.99) of the four compounds were found, which suggested that these compounds can be simultaneously determined with acceptable accuracy. Results showed that the plasma protein bindings of the four bioactive flavonoids were in the range of 74–89% over the six concentrations studied. The binding parameters containing protein binding affinity, protein binding dissociation constant, and protein binding site were studied. The maximum ability to bind with protein was also determined in the assay in order to understand the drug-protein binding of each compound better.
机译:开发了一种简单,选择性的超高效液相色谱-电喷雾电离串联质谱(UPLC-ESI-MS / MS)测定法,用于测定东方gon中四种生物活性类黄酮(如Orientin和Vitexin)与人血浆蛋白的结合。蛋白沉淀用于样品制备。应用平衡透析技术确定生理条件下血浆蛋白的结合。分离是通过沃特世C18色谱柱进行的,其中使用的流动相由0.1%的乙腈甲酸和0.1%的甲酸水溶液组成,采用逐步梯度洗脱法以0.35 mL / min的流速进行分离。 Waters ACQUITY™TQD系统在正电喷雾电离的多反应监测(MRM)模式下运行。该方法的所有回收率,精密度,准确性和稳定性均符合要求。发现这四种化合物具有良好的相关性(r> 0.99),这表明可以以可接受的准确度同时测定这些化合物。结果表明,在所研究的六个浓度下,四种生物活性类黄酮的血浆蛋白结合率在74–89%的范围内。研究了包含蛋白质结合亲和力,蛋白质结合解离常数和蛋白质结合位点的结合参数。在测定中还确定了与蛋白质结合的最大能力,以便更好地了解每种化合物的药物-蛋白质结合。

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