Rapid determination of five common toxic alkaloids in blood by UPLC–MRM–IDA–EPI: Application to poisoning case

•An UPLC–MS/MS method was developed for qualitative and quantitative analysis of five common toxic alkaloids.•Analyses of five common alkaloids in human postmortem blood were performed.•The method could be useful for forensic toxicological analysis. Toxic alkaloids are typically found in herbal medi...

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Veröffentlicht in:Legal medicine (Tokyo, Japan) Japan), 2023-07, Vol.63, p.102267-102267, Article 102267
Hauptverfasser: Zhang, Shan, Chen, Shunqin, Zhu, Faze, Wang, Aimin, Xia, Bing, Wang, Jie, Huang, Jiang, Liu, Yubo, Luo, Peng
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Sprache:eng
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Zusammenfassung:•An UPLC–MS/MS method was developed for qualitative and quantitative analysis of five common toxic alkaloids.•Analyses of five common alkaloids in human postmortem blood were performed.•The method could be useful for forensic toxicological analysis. Toxic alkaloids are typically found in herbal medicines and have strong pharmacological effects and a broad therapeutic spectrum. On the other hand, toxic alkaloids exert toxicological activities in vivo; as such they have a narrow therapeutic window and can induce poisoning due to incorrect dose or misuse. In this view, there is an urgent need to develop a rapid and sensitive assay to detect these toxic alkaloids. This study developed a method for determining five common toxic alkaloids in blood, including brucine, strychnine, aconitine, mesaconitine, and hypaconitine using ultra-high liquid chromatography-tandem quadrupole/linear ion trap mass spectrometry (QTRAP UPLC–MS/MS). The analytes in this investigation were extracted with ether and detected using multiple reaction monitoring (MRM)-information-dependent acquisition (IDA)-enhanced product ion (EPI) scanning modes. SKF525A served as the internal standard (IS). The approach demonstrated excellent linearity, with a correlation coefficient (R) > 0.9964, and satisfactory sensitivity, with the limit of detection (LOD) of 0.31 ∼ 3.26 ng/mL and a limit of quantification (LOQ) of 1.13 ∼ 11.52 ng/mL. The extraction recovery (ER) was 78.8 ∼ 116.2%, the matrix effect (ME) was −12.3 ∼ 21.2%, and the method accuracy was 0.8 ∼ 12.8%. In addition, the intra-day precision and the inter-day precision (RSD) were 0.7% ∼ 7.4% and 0.4% ∼ 13.5%, respectively. The developed approach is sensitive and efficient, and offer significant application prospect in clinical monitoring and forensic detection of poisoning.
ISSN:1344-6223
1873-4162
DOI:10.1016/j.legalmed.2023.102267