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建立并验证一种基于 UHPLC-MS/MS 的人血浆样品中苯巴比妥酸浓度的定量分析方法。

Development and Validation of a UHPLC-MS/MS-Based Method to Quantify Cenobamate in Human Plasma Samples.

机构信息

Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, 84081 Salerno, Italy.

University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131 Salerno, Italy.

出版信息

Molecules. 2022 Oct 28;27(21):7325. doi: 10.3390/molecules27217325.

Abstract

Cenobamate (CNB) is the newest antiseizure medication (ASM) approved by the FDA in 2019 to reduce uncontrolled partial-onset seizures in adult patients. Marketed as Xcopri in the USA or Ontozry in the EU (tablets), its mechanism of action has not been fully understood yet; however, it is known that it inhibits voltage-gated sodium channels and positively modulates the aminobutyric acid (GABA) ion channel. CNB shows 88% of oral bioavailability and is responsible for modifying the plasma concentrations of other co-administered ASMs, such as lamotrigine, carbamazepine, phenytoin, phenobarbital and the active metabolite of clobazam. It also interferes with CYP2B6 and CYP3A substrates. Nowadays, few methods are reported in the literature to quantify CNB in human plasma. The aim of this study was to develop and validate, according to the most recent guidelines, an analytical method using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS) to evaluate CNB dosage in plasma samples. Furthermore, we provided a preliminary clinical application of our methodology by evaluating the pharmacokinetic parameters of CNB in two non-adult patients. Plasma levels were monitored for two months. Preliminary data showed a linear increase in plasma CNB concentrations, in both patients, in agreement with the increase in CNB dosage. A seizure-free state was reported for both patients at the dose of 150 mg per day.

摘要

依诺肝素钠(CNB)是 2019 年美国食品药品监督管理局(FDA)批准的最新抗癫痫药物(ASM),用于减少成年患者部分性发作的癫痫发作。在美国以 Xcopri 上市,在欧盟以 Ontozry 上市(片剂),其作用机制尚未完全了解;然而,已知它抑制电压门控钠离子通道并正向调节γ-氨基丁酸(GABA)离子通道。CNB 的口服生物利用度为 88%,负责改变其他同时给药的 ASM(如拉莫三嗪、卡马西平、苯妥英、苯巴比妥和氯巴占的活性代谢物)的血浆浓度。它还干扰 CYP2B6 和 CYP3A 底物。目前,文献中报道的用于定量检测人血浆中 CNB 的方法很少。本研究旨在根据最新指南开发和验证一种使用超高效液相色谱-串联质谱(UHPLC-MS/MS)的分析方法,以评估血浆样品中 CNB 的剂量。此外,我们通过评估两名非成年患者的 CNB 药代动力学参数,对我们的方法进行了初步的临床应用。监测了两个月的血浆水平。初步数据显示,两名患者的血浆 CNB 浓度均呈线性增加,与 CNB 剂量的增加一致。两名患者在每天 150 毫克的剂量下均报告无癫痫发作状态。

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