Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
Anal Chim Acta. 2010 Jul 19;673(2):194-9. doi: 10.1016/j.aca.2010.05.030. Epub 2010 May 27.
Microemulsion electrokinetic capillary chromatography (MEEKC) with sample stacking induced by reverse migrating pseudostationary phase (SRMP) technique in a suppressed electro-osmotic flow (EOF) strategy was investigated for analysing the new ultra-short hypnotic HIE-124 in mice serum. The proposed method utilized fused-silica capillary with a total length of 50 cm (effective length 40 cm), applied voltages for stacking and separation were 5.0 kV for 4.30 min and subsequently 25 kV, respectively, with a sample injection of 0.5 psi for 90 s. All the runs were carried out at 25 degrees C and detected at 213 nm. The optimum microemulsion background electrolyte (BGE) solution consisted of 0.8% (v/v) ethyl acetate, 6.6% (v/v) butan-2-ol, 1.0% (v/v) acetonitrile, 2.0% (w/v) sodium dodecyl sulfate (SDS), and 89.6 mL with 25 mM phosphate buffer pH 8. When this preconcentration technique was used, the sample stacking and the separation processes took place successively with changing the voltage with an intermediate polarity switching step. The proposed method was validated carefully with respect to high specificity of the method, good linearity (r=0.9994), fair wide linear concentration range (66-1500 ng mL(-1)), limit of detection and quantitation were 21.6 and 65.5 ng mL(-1), respectively. The mean relative standard deviation (RSD) of the results of intra- and inter-day precision and accuracy were less than 6.0%, and overall recovery higher than 95% of HIE-124 in mice serum. The developed method could be used for the trace analyses of HIE-124 in serum and was finally used for the pharmacokinetic study investigation of HIE-124 in mice serum.
微乳液电动毛细管色谱(MEEKC)结合反迁移伪固定相(SRMP)技术的样品堆积和抑制电渗流(EOF)策略,用于分析新型超短催眠药物 HIE-124 在小鼠血清中的含量。该方法采用熔融石英毛细管,总长度为 50cm(有效长度 40cm),堆积和分离的施加电压分别为 5.0kV 持续 4.30min 和 25kV,样品进样为 0.5psi 持续 90s。所有运行均在 25°C 下进行,在 213nm 处检测。最佳微乳液背景电解质(BGE)溶液由 0.8%(v/v)乙酸乙酯、6.6%(v/v)仲丁醇、1.0%(v/v)乙腈、2.0%(w/v)十二烷基硫酸钠(SDS)和 89.6mL 25mM 磷酸盐缓冲液 pH8 组成。当使用这种浓缩技术时,通过中间极性切换步骤改变电压,成功地进行了样品堆积和分离过程。该方法具有高特异性、良好的线性(r=0.9994)、宽线性浓度范围(66-1500ng/mL)、检测限和定量限分别为 21.6 和 65.5ng/mL。日内和日间精密度和准确度的平均相对标准偏差(RSD)小于 6.0%,HIE-124 在小鼠血清中的总回收率高于 95%。该方法可用于血清中 HIE-124 的痕量分析,并最终用于小鼠血清中 HIE-124 的药代动力学研究。