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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Microanalytical study of sub-nanoliter samples by capillary electrophoresis - mass spectrometry with 100 % injection efficiency
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Microanalytical study of sub-nanoliter samples by capillary electrophoresis - mass spectrometry with 100 % injection efficiency

机译:注射效率为100%的毛细管电泳-质谱法对纳纳以下样品进行微量分析

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摘要

A method is presented for conducting fast capillary electrophoresis (CE) with ultrasmall sample volumes (< 10 nL) and subsequent determination of target analytes by time-of-flight mass spectrometry (TOF-MS). Furthermore, an approach towards preconcentration by solvent evaporation of samples as small as 500 nL is shown. Ultrasmall samples of biologically important cyclic nucleotides (cyclic guanosine monophosphate, cyclic adenosine monophosphate, cyclic cytidine monophosphate) served as model compounds. Sample volumes as small as 500 pL were used to perform sample uptake and CE injections by capillary batch injection (CBI). This resulted in detection limits between 2 and 5 fmol. The fast rate of sample evaporation prevents the operation of nano-/subnano-liter samples under room temperature conditions. A CBI-CE-TOF-MS setup incorporating a Peltier element and a thermostat was used for the handling of very small samples. In combination with tapered fused silica injection capillaries and the high-precision guiding system of the CBI setup, nearly 100 % efficient injections of ultrasmall samples into funnelled separation capillaries could be managed. The overall system allowed for high-throughput CE separations from densely arranged sample droplets or vials with RSD of peak heights ranging from 6 to 8 % (n = 5). CE-TOF-MS separations of mixtures of cyclic nucleotides were carried out in capillaries as short as 20 cm (25 mu m ID) in less than 55 s with high separation efficiency. We report details of the setup and optimizations with respect to etching of capillaries (tapering and funnelling), sample uptake and injection as well as separation of the model compounds. Moreover, the capabilities of the experimental setup for preconcentration of target analytes by solvent evaporation are described. Preconcentration factors of up to 100 could be achieved. This approach was successfully used for the determination of the cyclic nucleotide cGMP in (spiked) human urine samples.
机译:提出了一种使用超小样品量(<10 nL)进行快速毛细管电泳(CE)并随后通过飞行时间质谱(TOF-MS)测定目标分析物的方法。此外,显示了通过溶剂蒸发小至500 nL的样品进行预浓缩的方法。具有生物学重要性的环状核苷酸(环状鸟苷单磷酸酯,环状腺苷单磷酸酯,环状胞苷单磷酸酯)的超小型样品用作模型化合物。小至500 pL的样品量用于通过毛细管批量进样(CBI)进行样品摄取和CE进样。这导致检测限在2至5 fmol之间。样品蒸发速度快,阻止了纳升/亚纳升样品在室温条件下的运行。结合了珀耳帖元件和恒温器的CBI-CE-TOF-MS设置用于处理非常小的样品。结合锥形熔融石英进样毛细管和CBI装置的高精度引导系统,可以管理将近100%的超小样品高效进样到漏斗分离毛细管中。整个系统可实现高通量的CE分离,其分离的样品小滴或样品瓶的RSD的峰高范围为6%至8%(n = 5)。 CE-TOF-MS可以在短至20 cm(25μmID)的毛细管中在不到55 s的时间内完成环状核苷酸混合物的分离,分离效率很高。我们报告了关于毛细管腐蚀(锥度和漏斗),样品摄取和进样以及模型化合物分离的设置和优化的详细信息。此外,还介绍了通过溶剂蒸发对目标分析物进行预浓缩的实验装置的功能。可以实现高达100的预浓缩系数。该方法已成功用于测定(加标)人尿液样品中的环状核苷酸cGMP。

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