Arafa H M, Hamada F M, Elmazar M M, Nau H
Institut für Toxikologie und Embryopharmakologie, Freie Universität Berlin, Germany.
J Chromatogr A. 1996 Apr 5;729(1-2):125-36. doi: 10.1016/0021-9673(95)00980-9.
A fully automated reversed-phase HPLC method was developed for the quantitative assay of three retinoids (Am-580, CD-2019 and CD-437) which selectively activate the retinoic acid receptors RAR alpha, RAR beta and RAR gamma, respectively. Mouse plasma, embryo and maternal tissues were prepared for injection by on-line solid-phase extraction (SPE) and valve-switching techniques. Following automatic injection, the sample was loaded on preconditioned disposable cartridges, cleaned-up and then transferred onto the analytical column to be eluted in the backflush mode, separated by gradient elution and detected by UV, while a new cartridge was concomitantly conditioned. The overall recovery was quantitative allowing for external standardization. The calibration curves were linear in all biological samples tested so far, with a correlation coefficient (r) >0.99. The intra-day precision was < or = 7.8% (n = 5-6) and the inter-day variability was < or = 9.4% (n = 3). The lower limit of detection was 2.5 ng/ml or ng/g for CD-2019 and CD-437, and 5 ng/ml for Am-580 with a S/N ratio of 5 using a sample weight of 25 microliters or mg. The method is now in routine use in our laboratory for the assessment of the pharmacokinetic profiles of these retinoids. The small sample size required, the simple sample preparation and the rapid analysis with high degree of automation make this method convenient for microanalysis of biological samples both in animal and human studies.
建立了一种全自动反相高效液相色谱法,用于定量测定三种维甲酸(Am-580、CD-2019和CD-437),它们分别选择性激活维甲酸受体RARα、RARβ和RARγ。通过在线固相萃取(SPE)和阀切换技术制备小鼠血浆、胚胎和母体组织用于进样。自动进样后,将样品加载到预处理的一次性小柱上,进行净化,然后转移到分析柱上,以反冲模式洗脱,通过梯度洗脱分离并通过紫外检测,同时一个新的小柱进行同步预处理。总体回收率为定量,可进行外标法测定。到目前为止,在所有测试的生物样品中校准曲线均呈线性,相关系数(r)>0.99。日内精密度<或=7.8%(n = 5 - 6),日间变异<或=9.4%(n = 3)。对于CD-2019和CD-437,检测下限为2.5 ng/ml或ng/g,对于Am-580为5 ng/ml,使用25微升或毫克的样品重量时信噪比为5。该方法目前在我们实验室常规用于评估这些维甲酸的药代动力学特征。所需样品量小、样品制备简单且具有高度自动化的快速分析,使得该方法在动物和人体研究中对生物样品的微量分析都很方便。