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仪器对小口径柱超高效液相色谱中的分辨率和灵敏度的贡献:二极管阵列和三重四极杆质谱检测的比较。

Instrument contributions to resolution and sensitivity in ultra high performance liquid chromatography using small bore columns: comparison of diode array and triple quadrupole mass spectrometry detection.

机构信息

Agilent Technologies R&D and Marketing GmbH, Hewlett Packard-Strasse 8, 76337 Waldbronn, Germany.

Agilent Technologies Inc., 5301 Stevens Creek Blvd, Santa Clara, CA 95051-7201, USA.

出版信息

J Chromatogr A. 2015 Jan 16;1377:64-74. doi: 10.1016/j.chroma.2014.11.086. Epub 2014 Dec 9.

DOI:10.1016/j.chroma.2014.11.086
PMID:25547218
Abstract

UHPLC with DAD-UV detection or in combination with mass spectrometry (MS) has proven to be a robust and widely applicable platform for high sensitivity analyses of many types of chemical compounds. The majority of users employ narrow bore columns with 2.1mm internal diameter (ID) typically exhibiting very high efficiencies (>200,000 plates/m). This ultimately sets stringent demands upon the chromatographic system as the separation efficiency can be compromised by external contributions to dispersion caused by connection capillaries, auto-sampler and/or the detection device. Sample limited applications often use reduced column diameters down to capillary- or even nano-column format. Capillary (ID≤0.5mm) or small-bore columns (ID≤1mm) can be a good compromise between system robustness and enhanced sensitivity. Yet in this case, extra-column dispersion gains additional importance due to reduced peak volumes. To design an optimized system configuration for specific column dimensions and applications it is crucial to understand the dispersion contributions of individual extra-column components. This was subject to many studies done within our group and by others. Here, we employed a fully optimized UHPLC/UV system to investigate the contribution to peak dispersion obtained from columns ranging from capillary to narrow bore (0.3, 0.5, 1, 2.1mm) using a set of small molecules that were analyzed in gradient mode. Further UV detection was replaced by a triple quadrupole (QQQ) MS in order to evaluate its contribution to band broadening. In this context the impact of column-ID upon MS sensitivity when interfaced with an Agilent Jet Stream source was investigated. Data obtained from our test suite of compounds shows mostly mass-sensitive behavior of this advanced electrospray technology.

摘要

超高效液相色谱(UHPLC)与二极管阵列检测(DAD-UV)或与质谱(MS)联用已被证明是一种强大且广泛适用于多种类型化合物高灵敏度分析的平台。大多数用户使用内径为 2.1mm 的窄径柱,通常具有非常高的效率(>200,000 板/米)。这最终对色谱系统提出了严格的要求,因为由于连接毛细管、自动进样器和/或检测装置对外部分散的贡献,分离效率可能会受到影响。样品有限的应用通常使用减小的柱径,降至毛细管甚至纳升级别的柱径。毛细管(ID≤0.5mm)或小口径柱(ID≤1mm)在系统的稳健性和增强的灵敏度之间可以达到良好的平衡。然而,在这种情况下,由于峰体积减小,柱外分散会变得更加重要。为了针对特定的柱尺寸和应用设计优化的系统配置,了解各个柱外组件的分散贡献至关重要。这是我们小组和其他小组进行的许多研究的主题。在这里,我们使用完全优化的 UHPLC/UV 系统,使用一组在梯度模式下分析的小分子,研究了从毛细管到窄径(0.3、0.5、1、2.1mm)的柱子获得的峰分散对峰分散的贡献。进一步将紫外检测替换为三重四极杆(QQQ)MS,以评估其对带宽变宽的贡献。在这种情况下,当与安捷伦射流流源接口时,考察了柱内径对 MS 灵敏度的影响。从我们的化合物测试套件中获得的数据主要显示了这种先进的电喷雾技术的质量敏感行为。

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