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LC-ESI-MS-MS Determination of Rat Plasma Protein Binding of Major Flavonoids of Flos Lonicerae Japonicae by Centrifugal Ultrafiltration

机译:离心超滤-LC-ESI-MS-MS法测定金银花中主要类黄酮的大鼠血浆蛋白结合

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Centrifugal ultrafiltration (CU) and a fast liquid chromatography with electrospray ionization tandem mass spectrometric (LC-ESI-MS-MS) method have been developed for drug-protein binding analysis of four flavonoids of Flos Lonicerae Japonicae (FLJ). A rapid separation of free drug from the plasma was achieved by CU and the simultaneous analysis of four flavonoids of FLJ in rat plasma was by fast LC-ESI-MS-MS. The chromatographic analytical time decreased to 6.5 min without sacrificing resolution using a 4.6 mm × 50 mm, 1.8 μm particle size reverse phase column and MS–MS mode performed for multiple reaction monitoring (MRM). The protein binding rates of four flavonoids were in the range of 66.8 ± 7.4 to 81.3 ± 5.1% after oral administration of the flavonoid fraction of FLJ. All values were almost similar to 70.0% at 30, 45 and 80 min. Its result suggests that these flavonoids in rat plasma perform high protein binding rates and present a stable binding in a longer time. Meanwhile, it reveals that the elimination of these flavonoids may be relatively moderate in the body, the performance of a certain degree of accumulation may be speculated and make further impacts on the pharmacokinetic parameters.
机译:已经开发了离心超滤(CU)和带电喷雾电离串联质谱(LC-ESI-MS-MS)方法的快速液相色谱法,用于对金银花(FLJ)的四种类黄酮进行药物-蛋白质结合分析。通过CU快速分离血浆中的游离药物,并通过快速LC-ESI-MS-MS同时分析大鼠血浆中FLJ的四种黄酮。使用4.6 mm×50 mm,1.8μm粒径的反相色谱柱和用于多反应监测(MRM)的MS-MS模式,色谱分析时间缩短至6.5分钟,而不会牺牲分离度。口服FLJ的类黄酮部分后,四种类黄酮的蛋白结合率在66.8±7.4至81.3±5.1%的范围内。在30、45和80分钟时,所有值几乎都接近70.0%。其结果表明,大鼠血浆中的这些类黄酮具有较高的蛋白质结合率,并在较长的时间内呈现出稳定的结合。同时,它揭示了这些类黄酮在体内的消除可能相对适度,推测了一定程度的蓄积性能,并进一步影响了药代动力学参数。

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