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一种用于检测血清中河豚毒素和乌头生物碱的柱切换液相色谱/质谱/电喷雾电离方法。

A column-switching LC/MS/ESI method for detecting tetrodotoxin and Aconitum alkaloids in serum.

作者信息

Hayashida Makiko, Hayakawa Hideyuki, Wada Kentaro, Yamada Takeshi, Nihira Makoto, Ohno Youkichi

机构信息

Department of Legal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113-8602, Japan.

出版信息

Leg Med (Tokyo). 2003 Mar;5 Suppl 1:S101-4. doi: 10.1016/s1344-6223(02)00076-7.

Abstract

A liquid chromatography-mass spectrometry-electrospray ionization (LC/MS/ESI) method coupled with a column-switching technique has been developed for the determination of tetrodotoxin (TTX) and Aconitum alkaloids and their metabolites, such as aconitine, mesaconitine, hypaconitine, jesaconitine, benzoylaconine, benzoylmesaconine, benzoylhypaconine and 14-anisoylaconine, in serum. An on-column column-switching technique was employed to analyze TTX and Aconitum alkaloids and their metabolites without pretreatment of the serum. Combination of a multimode column with reversed phases and cation exchange for TTX, and use of a multimode column with reversed phases and a hydrophobic polymer column for Aconitum alkaloids and their metabolites provided successful separation and MS determination in ESI positive mode. A 100 microl serum sample was directly injected into a precolumn. For TTX monitored at m/z 320.1 in the selected ion monitoring mode, the calibration curve was linear within the range 0.1-100 ng/ml and the limit of detection was 0.1 ng/ml. For aconitine, mesaconitine, hypaconitine and jesaconitine, linear calibration curves were obtained up to 500 ng/ml and the limit of detection ranged from 0.2 to 1 ng/ml. For benzoylaconine, benzoylmesaconine, benzoylhypaconine and 14-anisoylaconine, linear calibration curves were obtained up to 500 ng/ml and the limit of detection ranged from 2 to 50 ng/ml. Recoveries from serum samples were within the range 78-119% for all the compounds studied.

摘要

已开发出一种结合柱切换技术的液相色谱-质谱-电喷雾电离(LC/MS/ESI)方法,用于测定血清中的河豚毒素(TTX)和乌头生物碱及其代谢产物,如乌头碱、中乌头碱、次乌头碱、杰斯乌头碱、苯甲酰乌头碱、苯甲酰中乌头碱、苯甲酰次乌头碱和14-茴香酰乌头碱。采用柱上柱切换技术分析TTX和乌头生物碱及其代谢产物,无需对血清进行预处理。将用于TTX的具有反相和阳离子交换功能的多模式柱,与用于乌头生物碱及其代谢产物的具有反相和疏水聚合物柱功能的多模式柱相结合,在ESI正模式下实现了成功分离和质谱测定。将100微升血清样品直接注入预柱。在选择离子监测模式下以m/z 320.1监测TTX时,校准曲线在0.1-100 ng/ml范围内呈线性,检测限为0.1 ng/ml。对于乌头碱、中乌头碱、次乌头碱和杰斯乌头碱,校准曲线在高达500 ng/ml时呈线性,检测限在0.2至1 ng/ml之间。对于苯甲酰乌头碱、苯甲酰中乌头碱、苯甲酰次乌头碱和14-茴香酰乌头碱,校准曲线在高达500 ng/ml时呈线性,检测限在2至50 ng/ml之间。所研究的所有化合物在血清样品中的回收率在78-119%范围内。

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