4.7 Article

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

期刊

TALANTA
卷 165, 期 -, 页码 240-244

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2016.12.056

关键词

Laser-induced fluorescence; Confocal; Flow injection analysis; Narrow capillary; Hydrodynamic chromatography; DNA separation

资金

  1. National Institutes of Health [R21GM104526]
  2. Department of Energy [DE-SC0006351]
  3. Oklahoma Center for the Advancement of Science and Technology [AR14-015]
  4. U.S. Department of Energy (DOE) [DE-SC0006351] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

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 (similar to 70 fluorescein molecules or 12 yoctomole fluorescein), a wide LDR (greater than 3 orders of magnitude) and a small background signal drift (similar to 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-mu m-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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据