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具有纳摩尔检测限的共焦激光诱导荧光检测器,用于窄毛细管系统。

Confocal laser-induced fluorescence detector for narrow capillary system with yoctomole limit of detection.

机构信息

University of Oklahoma, Department of Chemistry and Biochemistry, Norman, OK 73019, USA.

Department of Chemistry, Lanzhou University, Lanzhou, Gansu 730000, China.

出版信息

Talanta. 2017 Apr 1;165:240-244. doi: 10.1016/j.talanta.2016.12.056. Epub 2016 Dec 23.

Abstract

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.

摘要

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。

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