Frommherz L, Köhler H, Brinkmann B, Lehr M, Beike J
Institute of Legal Medicine, University Hospital Münster, Roentgenstrasse 23, 48149 Münster, Germany.
Int J Legal Med. 2008 Mar;122(2):109-14. doi: 10.1007/s00414-007-0175-5. Epub 2007 Jun 14.
A method is described for liquid chromatography-mass spectrometry analysis of the cardio glycosides digoxin and digitoxin in biological samples. The method was optimized for use in the forensic field and, therefore, comprises the determination from whole blood and tissue samples. Sample cleanup by solid phase extraction (SPE) on a functionalized polymeric phase was sufficient to limit matrix suppression to <10% for all analytes. Chromatographic separation was achieved using an RP-8 column. Detection of the cardio glycosides was performed with electrospray ionization in the positive mode. The system was run in single ion monitoring mode, measuring the sodium adducts (M + Na)+ of the analyte and of the internal standard, respectively. The method was fully validated for the analysis of blood samples and was also successfully applied in forensic cases. The method was accurate and precise over a linear concentration range up to 50 ng/g blood. Lower limit of quantitation was 0.2 ng/g for digoxin and 2 ng/g for digitoxin, respectively. As deuterated analyte was used as internal standard, we also present a new microwave-enhanced method for the fast preparation of the labelled analyte within 20 min.
本文描述了一种用于生物样品中强心苷地高辛和洋地黄毒苷的液相色谱 - 质谱分析方法。该方法针对法医领域进行了优化,因此包括从全血和组织样品中进行测定。在功能化聚合物相上通过固相萃取(SPE)进行样品净化,足以将所有分析物的基质抑制限制在<10%。使用RP - 8柱实现色谱分离。强心苷的检测采用正模式电喷雾电离进行。该系统以单离子监测模式运行,分别测量分析物和内标的钠加合物(M + Na)+。该方法已针对血样分析进行了全面验证,并成功应用于法医案件。该方法在高达50 ng/g血液的线性浓度范围内准确且精密。地高辛和洋地黄毒苷的定量下限分别为0.2 ng/g和2 ng/g。由于使用氘代分析物作为内标,我们还提出了一种新的微波增强方法,可在20分钟内快速制备标记分析物。