开发并验证经 MEPS 处理的大鼠血浆样品中哌仑帕奈的 HPLC-FLD 分析方法

Ayah Nader Abu-shark, A. Shakya, Safwan M. Al-Adwan, R. Naik
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摘要

Perampanel是一种新型α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体拮抗剂,已注册用于难治性部分性癫痫发作患者(年龄≥12岁)的辅助治疗。我们开发了一种简单的高效液相色谱法荧光检测法(HPLC-FLD)来分析大鼠血浆中的 perampanel,并进行了生物分析验证。大鼠血浆(50 µL)经微萃取填充吸附剂(MEPS)处理。使用 Hypersil Gold 十八烷基硅烷色谱柱(内径 250 × 4.6 mm,粒径 5 μm)和等度洗脱分离分析物。流动相为乙腈-甲醇-水(275:275:450,v/v/v;含 50 µL 三乙胺,pH 值用正磷酸调节至 3.25)。流速为 1.25 mL/min。激发波长为 285 nm,发射波长为 430 nm。该方法的线性范围为 3.75 至 300 ng/mL。在无药大鼠血浆中的分析物洗脱过程中未发现内源性峰。批内和批间重现性研究表明,该方法的准确度和精密度均符合接受标准。结果表明,该方法简便、选择性好、重现性好,适用于小容量样品中哌仑帕奈的分析。使用 MODDE® 实验设计软件 12.5 版检测了该方法的稳健性。
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Development and Validation of HPLC-FLD Analysis of Perampanel in MEPS-Processed Rat Plasma Sample
Perampanel, a novel α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist, is registered for the adjunctive treatment of patients (aged ≥ 12 years) with refractory partial-onset seizures. A simple high-performance liquid chromatographic method fluorescence detection (HPLC-FLD) was developed to analyze perampanel in rats’ plasma and validated for bioanalytical purposes. Rats’ plasma (50 µL) was processed by microextraction packed sorbent (MEPS). The analytes were separated using a Hypersil Gold octadecyl silane column (250 × 4.6 mm internal diameter, 5 μm particle size) with isocratic elution. A mobile phase consisting of acetonitrile–methanol–water (275:275:450, v/v/v; containing 50 µL triethylamine and pH adjusted to 3.25 with orthophosphoric acid) was used in this analysis. The flow rate was 1.25 mL/min. Analytes were monitored at an excitation wavelength of 285 nm and an emission wavelength of 430 nm. The linearity range for this validated method was from 3.75 to 300 ng/mL. No endogenous peaks were found in the elution of analytes in drug-free rats’ plasma. Intra- and inter-batch reproducibility studies demonstrated accuracy and precision within the acceptance criteria. The results indicate that the present method is simple, selective, reproducible, and suitable for the analysis of perampanel in small volume samples. The robustness of the method was accessed using MODDE® design of experiments software version 12.5.
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