School of Pharmaceutical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
Anal Bioanal Chem. 2014 Jan;406(2):421-9. doi: 10.1007/s00216-013-7378-z. Epub 2013 Oct 3.
A small and very simple electromembrane extraction probe (EME-probe) was developed and coupled directly to electrospray ionization mass spectrometry (ESI-MS), and this system was used to monitor in real time in vitro metabolism by rat liver microsomes of drug substances from a small reaction (incubation) chamber (37 °C). The drug-related substances were continuously extracted from the 1.0 mL metabolic reaction mixture and into the EME-probe by an electrical potential of 2.5 V. The extraction probe consisted of a 1-mm long and 350-μm ID thin supported liquid membrane (SLM) of 2-nitrophenyl octyl ether. The drugs and formed metabolites where extracted through the SLM and directly into a 3 μL min(-1) flow of 60 mM HCOOH inside the probe serving as the acceptor solution. The acceptor solution was directed into the ESI-MS-system, and the MS continuously monitored the drug-related substances extracted by the EME-probe. The extraction efficiency of the EME-probe was dependant on the applied electrical potential and the length of the SLM, and these parameters as well as the volume of the reaction chamber were set to the values mentioned above to avoid serious depletion from the reaction chamber (soft extraction). Soft extraction was mandatory in order not to affect the reaction kinetics by sample composition changes induced by the EME-probe. The EME-probe/MS-system was used to establish kinetic profiles for the in vitro metabolism of promethazine, amitriptyline and imipramine as model substances.
开发了一种小型且非常简单的电膜萃取探头(EME 探头),并将其直接与电喷雾电离质谱(ESI-MS)耦合,该系统用于实时监测大鼠肝微粒体在小反应(孵育)室(37°C)中对药物物质的体外代谢。通过 2.5 V 的电势,将与药物相关的物质从 1.0 mL 代谢反应混合物中连续提取到 EME 探头中。萃取探头由 1 毫米长和 350-μm ID 的 2-硝基苯基辛基醚薄支撑液膜(SLM)组成。药物和形成的代谢物通过 SLM 被提取,并直接进入探针内 3 μL min(-1) 的 60 mM HCOOH 流动作为接受溶液。接受溶液被引导进入 ESI-MS 系统,MS 连续监测 EME 探头提取的与药物相关的物质。EME 探头的萃取效率取决于所施加的电势和 SLM 的长度,这些参数以及反应室的体积被设置为上述值,以避免因探针引起的样品组成变化而严重耗尽反应室(软萃取)。软萃取是必需的,以免通过 EME 探头引起的样品组成变化影响反应动力学。EME 探头/MS 系统用于建立普罗米嗪、阿米替林和丙咪嗪作为模型物质的体外代谢动力学谱。