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一种用于低水平测定 pemafibrate 的经验证的 LC-MS/MS 方法,pemafibrate 是一种新型 SPPARMα,在血浆中。

A validated LC-MS/MS method for the low-level determination of pemafibrate, a novel SPPARMα, in plasma.

机构信息

Department of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607 8414, Japan.

出版信息

Bioanalysis. 2020 May;12(10):683-692. doi: 10.4155/bio-2020-0081. Epub 2020 Jun 3.

Abstract

Pemafibrate, a novel selective peroxisome proliferator-activated receptor-α modulator, is prescribed for patients with dyslipidemia. To investigate other potential nonlipid-related effects of pemafibrate, the sensitive and rapid quantitation method for pemafibrate was required. The developed LC-MS/MS assay method exhibited excellent accuracy, precision, sensitivity, stability, no matrix effect and high recovery. The LOQ (0.05 ng/ml) and run time (6.0 min) were superior to previous reports. The calibration curve showed good linearity over the wide concentration range (0.05-100.00 ng/ml). This validated method was successfully applied in a rat pharmacokinetic study using lower doses (0.02 or 0.10 mg/kg) than have been previously reported. This method can support gathering data for the evaluation of pemafibrate in future studies.

摘要

非诺贝特是一种新型的选择性过氧化物酶体增殖物激活受体-α调节剂,用于治疗血脂异常。为了研究非诺贝特的其他潜在非脂质相关作用,需要一种灵敏、快速的非诺贝特定量方法。所建立的 LC-MS/MS 检测方法具有良好的准确度、精密度、灵敏度、稳定性、无基质效应和高回收率。该方法的定量下限(0.05ng/ml)和运行时间(6.0 分钟)优于以往的报道。在较宽的浓度范围内(0.05-100.00ng/ml),校准曲线显示出良好的线性关系。该方法已成功应用于大鼠药代动力学研究,所用剂量(0.02 或 0.10mg/kg)低于以往报道的剂量。该方法可以支持在未来的研究中收集非诺贝特的数据。

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