University of Oklahoma, Department of Chemistry and Biochemistry, Norman, OK 73019, USA.
Department of Chemistry, Lanzhou University, Lanzhou, Gansu 730000, China.
Talanta. 2017 Apr 1;165:240-244. doi: 10.1016/j.talanta.2016.12.056. Epub 2016 Dec 23.
Laser-induced fluorescence (LIF) detectors for low-micrometer and sub-micrometer capillary on-column detection are not commercially available. In this paper, we describe in details how to construct a confocal LIF detector to address this issue. We characterize the detector by determining its limit of detection (LOD), linear dynamic range (LDR) and background signal drift; a very low LOD (70 fluorescein molecules or 12 yoctomole fluorescein), a wide LDR (greater than 3 orders of magnitude) and a small background signal drift (1.2-fold of the root mean square noise) are obtained. For detecting analytes inside a low-micrometer and sub-micrometer capillary, proper alignment is essential. We present a simple protocol to align the capillary with the optical system and use the position-lock capability of a translation stage to fix the capillary in position during the experiment. To demonstrate the feasibility of using this detector for narrow capillary systems, we build a 2-μm-i.d. capillary flow injection analysis (FIA) system using the newly developed LIF prototype as a detector and obtain an FIA LOD of 14 zeptomole fluorescein. We also separate a DNA ladder sample by bare narrow capillary - hydrodynamic chromatography and use the LIF prototype to monitor the resolved DNA fragments. We obtain not only well-resolved peaks but also the quantitative information of all DNA fragments.
用于微柱和亚微柱柱上检测的激光诱导荧光(LIF)检测器在商业上不可用。本文详细介绍了如何构建共焦 LIF 检测器来解决这个问题。我们通过确定其检测限(LOD)、线性动态范围(LDR)和背景信号漂移来表征检测器;获得了非常低的 LOD(70 个荧光素分子或 12 个飞摩尔荧光素)、宽的 LDR(大于 3 个数量级)和小的背景信号漂移(1.2 倍的均方根噪声)。对于检测微柱和亚微柱内的分析物,正确的对准是必不可少的。我们提出了一种简单的协议来对准毛细管和光学系统,并使用平移台的位置锁定功能在实验过程中固定毛细管的位置。为了证明使用这种检测器进行窄毛细管系统的可行性,我们使用新开发的 LIF 原型作为检测器构建了 2-μm-i.d.毛细管流动注射分析(FIA)系统,并获得了 14 飞摩尔荧光素的 FIA LOD。我们还通过裸窄毛细管 - 水动力色谱分离 DNA 梯样,并使用 LIF 原型监测分离的 DNA 片段。我们不仅获得了良好分离的峰,还获得了所有 DNA 片段的定量信息。