首页> 外文期刊>International journal of analytical chemistry >An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study
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An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study

机译:一种LC-MS / MS方法,用于同时测定大鼠血浆中皮质Periplocae的毒性和活性成分及其在药代动力学研究中的应用

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A sensitive and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated to simultaneously determine the toxic and other active components including isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of cortex periplocae extract to rats. Plasma samples were prepared by protein precipitation with methanol. All compounds were separated on a C18 column with gradient elution using acetonitrile and formic acid aqueous solution (0.1%, v/v) as the mobile phase at a flow rate of 0.3 mL/min. The detection of all compounds was accomplished by multiple-reaction monitoring (MRM) in the positive electrospray ionization mode. The LC-MS/MS method exhibited good linearity for five analytes. The lower limit of quantification (LLOQ) was 0.48 ng/mL for scopoletin, periplogenin, and periplocymarin; 2.4 ng/mL for isovanillin and periplocin. The extraction recoveries of all compounds were more than 90% and the RSDs were below 10%. It was found that the absorption of scopoletin and periplocin was rapid in vivo after oral administration of cortex periplocae extract. Furthermore, periplocymarin possessed abundant plasma exposure. The results demonstrated that the validated method was efficiently applied for the pharmacokinetic studies of isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of cortex periplocae extract.
机译:开发并验证了一种敏感和简单的液相色谱 - 串联质谱(LC-MS / MS)方法,以同时测定毒性和其他活性成分,包括胰岛素蛋白,Scopoletin,Periplocin,Periplogenin和Periplocymarin的口服施用皮层Periplocae提取物老鼠。通过蛋白质沉淀用甲醇制备等离子体样品。将所有化合物在C18柱上分离,使用乙腈和甲酸水溶液(0.1%,v / v)作为流动率,以0.3ml / min的流速,以梯度洗脱。通过阳性电喷雾电离模式中的多反应监测(MRM)完成所有化合物的检测。 LC-MS / MS方法表现出五种分析物的良好线性。用于微型素,胰岛素原和细胞素素的量化(LLOQ)的下限为0.48ng / ml;对于异维蛋白和Periplocin 2.4ng / ml。所有化合物的提取回收率大于90%,RSD低于10%。发现在口服施用皮层Periplocae提取物后体内缓慢的缓解素和Periplocin的吸收。此外,Periplocymarin具有丰富的血浆暴露。结果表明,香加皮提取物的口服给药之后的验证的方法被有效应用于异香草醛,东莨菪亭的药代动力学研究,杠柳,杠柳苷,和periplocymarin。

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