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新型 AMPA 受体拮抗剂吡仑帕奈在 SD 大鼠中的药代动力学和脑内摄取研究:一种已验证的 UHPLC-QTOF-MS 方法。

Pharmacokinetics and brain uptake study of novel AMPA receptor antagonist perampanel in SD rats using a validated UHPLC-QTOF-MS method.

机构信息

Drug Metabolism and Interactions Research Lab, Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, Telangana, 500037, India.

Drug Metabolism and Interactions Research Lab, Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, Telangana, 500037, India.

出版信息

J Pharm Biomed Anal. 2018 Feb 5;149:234-241. doi: 10.1016/j.jpba.2017.11.008. Epub 2017 Nov 8.

Abstract

Perampanel (PER) is a novel AMPA receptor antagonist for antiepileptic therapy and is prospective for the treatment of other neurological disorders. A highly sensitive and rapid UHPLC-QTOF-MS method was developed for the quantification of PER in plasma/brain homogenate of SD rat with alogliptin as an internal standard (IS). Chromatographic separation was carried out on an Acquity UPLC HSS Cyano column (100mm×2.1mm, 1.8μm) using gradient mobile phase consisting of 0.1% formic acid and acetonitrile at a flow rate of 0. 4mL/min. Sample preparation was carried out by a simple protein precipitation method. The mass spectrometric analysis of target ions at [M+H]m/z 350.1288 for PER and m/z 340.1779 for IS was monitored with extracted ion chromatography. The developed analytical method meets the US-FDA and EMA bioanalytical guidelines and was found to be precise, accurate, selective and rugged. It exhibited good sensitivity (0.4ng/mL) and linearity over a range of 0.4-400ng/mL in both the bio-matrices. The method was successfully applied to pharmacokinetics and brain uptake study of PER after oral administration to SD rats. The study results showed PER has penetrated the blood-brain barrier, brain to plasma ratio (Kp) was found to be 0.62±0.05 and its rapidly eliminated from the brain.

摘要

吡仑帕奈(PER)是一种新型 AMPA 受体拮抗剂,用于抗癫痫治疗,有望用于治疗其他神经疾病。本研究建立了一种灵敏、快速的 UHPLC-QTOF-MS 法,用于测定 SD 大鼠血浆/脑匀浆中吡仑帕奈的浓度,阿格列汀为内标(IS)。色谱柱为 Acquity UPLC HSS Cyano 柱(100mm×2.1mm,1.8μm),以 0.1%甲酸-乙腈为流动相进行梯度洗脱,流速为 0.4mL/min。采用简单的蛋白沉淀法进行样品前处理。采用提取离子色谱法,对目标离子[M+H]+m/z 350.1288(PER)和 m/z 340.1779(IS)进行监测。所建立的分析方法符合美国 FDA 和欧洲 EMA 的生物分析指导原则,具有良好的准确性、精密度、选择性和耐用性。在两种生物基质中,其线性范围均为 0.4-400ng/mL,检测限为 0.4ng/mL。该方法成功应用于 SD 大鼠灌胃给予吡仑帕奈后的药代动力学和脑内分布研究。结果表明,吡仑帕奈能够透过血脑屏障,脑内药物浓度与血药浓度的比值(Kp)为 0.62±0.05,其在脑内迅速消除。

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