Ke Yuyong, Gonthier Renaud, Labrie Fernand
EndoCeutics Inc., 2795 Laurier Blvd, Suite 500, Quebec City, QC G1V 4M7, Canada.
EndoCeutics Inc., 2795 Laurier Blvd, Suite 500, Quebec City, QC G1V 4M7, Canada.
Steroids. 2017 Feb;118:25-31. doi: 10.1016/j.steroids.2016.11.007. Epub 2016 Nov 29.
The concentrations of allopregnanolone (Allopreg), pregnenolone (Preg) and androsterone (ADT) are very low in the circulation, especially in postmenopausal women, resulting in a considerable challenge for their accurate measurements in serum or plasma. In this report, a sensitive and reliable LC-MS/MS assay method has been developed using a simple sample preparation and the 1-Amino-4-methylpiperazine (AMP) derivatization procedure. A 5pg/ml (0.1pg on column) of low limit of quantitation has been achieved for Allopreg, Preg and ADT, with a sensitivity comparable to data obtained with the commercial reagent. The major benefit of this reagent is to limit the matrix effect since the excess amount of reagent can be removed during the reaction. Multiple reaction monitoring (MRM) from the derivatization of AMP not only increases the detection of these compounds but also provides a good resolution for Allopreg, Preg and ADT from interferences, especially for Allopreg from its isomers. Within the calibration range of 5pg/ml to 2000pg/ml, a good linearity was obtained with R>0.99 where the weighing factor is 1/X. Bias and coefficients of variance are within 15% for all QC levels. The matrix effect has been evaluated, well meeting the acceptance criteria according to the FDA guidelines. With this method, the concentrations of Allopreg, Preg and ADT in postmenopausal serum are in the range of 6.4-53.6pg/ml, 16.2-68.0pg/ml and 23.9-114.0pg/ml, respectively, while the ranges in premenopausal serum are 8.2-701.5pg/ml, 31.2-135.2pg/ml and 47.8-310.0pg/ml, respectively.
别孕烯醇酮(Allopreg)、孕烯醇酮(Preg)和雄酮(ADT)在循环系统中的浓度非常低,尤其是在绝经后女性中,这给在血清或血浆中准确测量它们带来了相当大的挑战。在本报告中,已开发出一种灵敏且可靠的液相色谱-串联质谱(LC-MS/MS)检测方法,该方法采用简单的样品制备和1-氨基-4-甲基哌嗪(AMP)衍生化程序。Allopreg、Preg和ADT的定量下限达到5pg/ml(柱上0.1pg),灵敏度与使用商业试剂获得的数据相当。该试剂的主要优点是限制基质效应,因为过量的试剂可在反应过程中去除。AMP衍生化后的多反应监测(MRM)不仅提高了这些化合物的检测能力,还为Allopreg、Preg和ADT与干扰物提供了良好的分离度,特别是Allopreg与其异构体的分离。在校准范围5pg/ml至2000pg/ml内,获得了良好的线性关系,R>0.99,加权因子为1/X。所有质量控制水平的偏差和变异系数均在15%以内。已评估了基质效应,完全符合美国食品药品监督管理局(FDA)指南的验收标准。采用该方法,绝经后血清中Allopreg、Preg和ADT的浓度分别在6.4 - 53.6pg/ml、16.2 - 68.0pg/ml和23.9 - 114.0pg/ml范围内,而绝经前血清中的范围分别为8.2 - 701.5pg/ml、31.2 - 135.2pg/ml和47.8 - 310.0pg/ml。