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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 >Development and validation of LC-MS/MS method for quantification of pseudolaric acid B from the root bark of Pseudolarix kaempferi in rat plasma: Application to a pharmacokinetic study
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Development and validation of LC-MS/MS method for quantification of pseudolaric acid B from the root bark of Pseudolarix kaempferi in rat plasma: Application to a pharmacokinetic study

机译:LC-MS / MS法测定和鉴定大鼠血浆假单胞菌根皮中假胡闹酸B的方法开发和验证:在药代动力学研究中的应用

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摘要

Pseudolaric acid B (PAB), which is the main biologically active diterpene acid of Pseudolarix kaempferi, has presented anti-fungal, anti-tumor, anti-fertility, and anti-tubulin activities. In this study, a sensitive and selective liquid chromatography tandem mass spectrometry (LC-MS/MS) method with multiple-reaction monitoring mode was employed for quantification of PAB in rat plasma. The calibration curve was linear over the range of 0.86-288 ng/mL with correlation coefficient (r) greater than 0.995 for PAB, and the lower limit of quantification was 0.86 ng/mL in rat plasma. The accuracy of PAB was between -9.1% and 7.0% relative error, and precision ranged from 1.2 to 10.6% relative standard deviation. This method was successfully applied to the pharmacokinetic studies of PAB in Sprague-Dawley rats. After single intravenous administration of 2.0, 4.0, and 8.0 mg/kg PAB to rats, the to were (16.1 +/- 5.6), (30.0 +/- 13.7),. and (27.4 +/- 5.3) min, respectively. The pharmacokinetics (C-2min, AUC) of PAB within the used dosage range were in accordance with linear pharmacokinetic characteristics. (C) 2015 Elsevier B.V. All rights reserved.
机译:拟南芥中的主要生物活性二萜酸伪laric B(PAB)具有抗真菌,抗肿瘤,抗生育和抗微管蛋白的活性。在这项研究中,采用多反应监测模式的灵敏选择性液相色谱串联质谱法(LC-MS / MS)定量大鼠血浆中的PAB。校准曲线在0.86-288 ng / mL的范围内呈线性,PAB的相关系数(r)大于0.995,在大鼠血浆中的定量下限为0.86 ng / mL。 PAB的相对误差在-9.1%至7.0%之间,相对误差在1.2至10.6%之间。该方法已成功地应用于Sprague-Dawley大鼠中PAB的药代动力学研究。在向大鼠单次静脉内注射2.0、4.0和8.0 mg / kg PAB后,to为(16.1 +/- 5.6),(30.0 +/- 13.7)。和(27.4 +/- 5.3)分钟。在所用剂量范围内,PAB的药代动力学(C-2min,AUC)与线性药代动力学特征一致。 (C)2015 Elsevier B.V.保留所有权利。

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