Kawaguchi Migaku, Eyama Sakae, Takatsu Akiko
Bio-Medical Standard Section, National Metrology Institute of Japan (NMIJ), National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Umezono, Tsukuba, Ibaraki 305-8563, Japan.
Bio-Medical Standard Section, National Metrology Institute of Japan (NMIJ), National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Umezono, Tsukuba, Ibaraki 305-8563, Japan.
J Pharm Biomed Anal. 2014 Aug 5;96:220-3. doi: 10.1016/j.jpba.2014.03.015. Epub 2014 Apr 3.
A candidate reference measurement procedure involving automated isotope dilution coupled with liquid chromatography-tandem mass spectrometry (ID-LC-MS/MS) with on-line dilution and solid phase extraction (SPE) has been developed and critically evaluated. We constructed the LC-MS/MS with on-line dilution and SPE system. An isotopically labelled internal standard, cortisol-d4, was added to serum sample. After equilibration, the methanol was added to the sample, and deproteination was performed. Then, the sample was applied to the LC-MS/MS system. The limit of detection (LOD) and limit of quantification (LOQ) were 0.2 and 1ngg(-1), respectively. Excellent precision was obtained with within-day variation (RSD) of 1.9% for ID-LC-MS/MS analysis (n=6). This method, which demonstrates simple, easy, good accuracy, high precision, and is free from interferences from structural analogues, qualifies as a reference measurement procedure.
已开发并严格评估了一种候选参考测量程序,该程序涉及自动同位素稀释结合液相色谱 - 串联质谱法(ID-LC-MS/MS)以及在线稀释和固相萃取(SPE)。我们构建了具有在线稀释和SPE系统的LC-MS/MS。将同位素标记的内标皮质醇 - d4添加到血清样品中。平衡后,向样品中加入甲醇并进行去蛋白处理。然后,将样品应用于LC-MS/MS系统。检测限(LOD)和定量限(LOQ)分别为0.2和1ng g(-1)。ID-LC-MS/MS分析的日内变异(RSD)为1.9%(n = 6),获得了出色的精密度。该方法简单、易行、准确度高、精密度高且不受结构类似物的干扰,符合参考测量程序的要求。