Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P. O. Box 2457, Riyadh 11451, Saudi Arabia.
Analyst. 2011 Feb 7;136(3):591-7. doi: 10.1039/c0an00381f. Epub 2010 Nov 16.
For the first time, a fast, high-performance liquid chromatography (HPLC) method was developed and validated for the simultaneous determination of the new ultra-short hypnotic HIE-124 and its metabolite in mice serum. Each compound, together with carbamazepine (internal standard) was extracted from the serum matrix using liquid-liquid extraction (LLE). Chromatographic resolution of the analytes was performed on a Chromolith Speed Rod monolithic silica column (100 mm × 4.6 mm i.d.) under isocratic conditions using a mobile phase of 65:35 (v/v), 20 mM phosphate buffer (pH 7.0 adjusted with phosphoric acid)-acetonitrile. The elution of the analytes were monitored at 240 nm and conducted at ambient temperature. Because of high column efficiency the mobile phase was pumped at a flow rate of 2.5 mL min(-1). The total run time of the assay was 2 min. The method was validated over the range of 60-2000 ng mL(-1) for HIE-124 and 200-1600 ng mL(-1) for the metabolite (r(2) = 0.99). The limit of detection (LOD) for HIE-124 and its metabolite were 20 ng mL(-1) and 65 ng mL(-1), respectively. The proposed method was validated in compliance with ICH guidelines, in terms of accuracy, precision, limits of detection and quantitation and other aspects of analytical validation. The developed method could be used for the trace analyses of HIE-124 and its metabolite in serum and was finally used for the pharmacokinetic study investigation of HIE-124 in mice serum.
首次建立并验证了一种快速、高效的液相色谱(HPLC)法,用于同时测定小鼠血清中的新型超短催眠药 HIE-124 及其代谢物。采用液液萃取(LLE)法从血清基质中提取各化合物和卡马西平(内标)。采用 65:35(v/v)、20 mM 磷酸盐缓冲液(用磷酸调 pH 值 7.0)-乙腈作为流动相,在 Chromolith Speed Rod 整体硅胶柱(100 mm×4.6 mm i.d.)上进行等度洗脱,在 240nm 处检测,室温下进行色谱分离。由于柱效高,将流动相以 2.5 mL min(-1)的流速泵入。分析时间为 2 min。该方法在 HIE-124 的检测范围为 60-2000ng mL(-1),代谢物的检测范围为 200-1600ng mL(-1)时,线性良好(r(2) = 0.99)。HIE-124 和代谢物的检测限(LOD)分别为 20ng mL(-1)和 65ng mL(-1)。该方法符合 ICH 指南的准确度、精密度、检测限和定量限以及分析验证的其他方面的要求。该方法可用于血清中 HIE-124 及其代谢物的痕量分析,最后用于小鼠血清中 HIE-124 的药代动力学研究。