CICS-UBI - Health Sciences Research Center, University of Beira Interior, Covilhã, Portugal.
UDI-IPG - Research Unit for Inland Development, Polytechnic Institute of Guarda, Guarda, Portugal.
J Sep Sci. 2020 Dec;43(23):4289-4304. doi: 10.1002/jssc.202000656. Epub 2020 Oct 20.
We report a high-performance liquid chromatography method development able to simultaneously determine perampanel and stiripentol, two third-generation antiepileptics whose therapeutic spectrum can potentially be extended, in several mouse matrices. A salting-out assisted liquid-liquid extraction optimized by a design of experiments approach was adopted for sample preparations. Isopropanol and magnesium sulfate were the extraction solvent and salting-out agent, respectively. Both drugs and internal standard (terbinafine) were separated using a LiChroCART Purospher Star column (C , 55 × 4 mm; 3 μm) isocratically pumped with mobile phase [1% triethylamine in water (pH 2.5) and acetonitrile (53:47, v/v)] at 1 mL/min. Stiripentol and terbinafine were detected by fluorescence at 254/372 nm and perampanel at 275/430 nm. Good linearity was demonstrated for perampanel at 1-500 ng/mL range in brain, 2-2000 ng/mL in liver and 1-2000 ng/mL in plasma and kidney (r ≥ 0.9922), and for stiripentol between 10 and 2000 ng/mL in brain and 10 and 20 000 ng/mL in the remaining matrices (r ≥ 0.9917). Precision (CV ≤ 15%) and accuracy (bias ±15%) were also verified, with obtained recovery values consistent with those predicted by the experimental design. This method was applied in preliminary pharmacokinetic studies to quantify perampanel or stiripentol after oral administration to mice, showing to be a promising bioanalytical tool to support future nonclinical in vivo pharmacokinetic studies.
我们报告了一种高效液相色谱法的开发,该方法能够同时测定两种第三代抗癫痫药物——吡仑帕奈和司替戊醇,这两种药物的治疗谱有可能得到扩展,可用于多种小鼠基质。采用实验设计方法优化了盐析辅助液液萃取法进行样品制备。异丙醇和硫酸镁分别为萃取溶剂和盐析剂。两种药物和内标(特比萘芬)均采用 LiChroCART Purospher Star 柱(C ,55×4mm;3μm)进行等度洗脱,流动相为 [1%三乙胺水溶液(pH 2.5)和乙腈(53:47,v/v)],流速为 1mL/min。司替戊醇和特比萘芬在 254/372nm 处用荧光检测,吡仑帕奈在 275/430nm 处用荧光检测。吡仑帕奈在脑、肝和血浆中的线性范围为 1-500ng/mL、2-2000ng/mL 和 1-2000ng/mL,肾中的线性范围为 1-500ng/mL(r ≥ 0.9922);司替戊醇在脑内的线性范围为 10-2000ng/mL,在其余基质中的线性范围为 10-20000ng/mL(r ≥ 0.9917)。还验证了精密度(CV≤15%)和准确度(偏差±15%),获得的回收率与实验设计预测值一致。该方法应用于初步的药代动力学研究,以定量口服给予小鼠后吡仑帕奈或司替戊醇,表明这是一种有前途的生物分析工具,可支持未来的非临床体内药代动力学研究。