Sotoudegan Farzaneh, Amini Mohsen, Faizi Mehrdad, Aboofazeli Reza
Department of Pharmaceutics, School of Pharmacy & Protein Technology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Iran J Pharm Res. 2017 Spring;16(2):471-477.
A rapid, simple and reproducible HPLC method was developed and validated for the analysis of nimodipine (NM) and/or its metabolite, oxidized nimodipine (OX-NM) in rat cerebrospinal fluid (CSF) and artificial CSF. The NM and OX-NM were eluted in less than 10 min with no interferences from the endogenous CSF peaks. Analysis was carried out on a Eurospher Performance (RP-C18, 250 × 4.6 mm) column and UV detection at 236 nm. The mobile phase consisted of acetonitrile and water (70:30 v/v, respectively) with a flow rate of 1 mL/min. Limit of detection was 0.1 μg/mL for OX-NM. The calibration curve was linear over the concentration range of 0.5-10 µg/mL and analytical recovery was more than 95%. The coefficients of variation for intra-day and inter-day assays were less than 5%.
建立了一种快速、简单且可重复的高效液相色谱法,并对其进行了验证,用于分析大鼠脑脊液(CSF)和人工脑脊液中尼莫地平(NM)和/或其代谢产物氧化尼莫地平(OX-NM)。NM和OX-NM在不到10分钟内洗脱出来,没有受到内源性脑脊液峰的干扰。分析在Eurospher Performance(RP-C18,250×4.6 mm)柱上进行,在236 nm处进行紫外检测。流动相由乙腈和水(分别为70:30 v/v)组成,流速为1 mL/min。OX-NM的检测限为0.1 μg/mL。校准曲线在0.5-10 µg/mL的浓度范围内呈线性,分析回收率超过95%。日内和日间测定的变异系数均小于5%。