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超高效液相色谱-电感耦合等离子体质谱联用测定硫代磷酸酯寡核苷酸的新方法。

New approach to the determination phosphorothioate oligonucleotides by ultra high performance liquid chromatography coupled with inductively coupled plasma mass spectrometry.

作者信息

Studzińska Sylwia, Mounicou Sandra, Szpunar Joanna, Łobiński Ryszard, Buszewski Bogusław

机构信息

Chair of the Environmental Chemistry & Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University, 7 Gagarin St., PL-87 100 Torun, Poland.

CNRS/UPPA, Laboratoire de Chimie Analytique Bio-inorganique et Environnement, UMR 5254, Hélioparc, 2 av. Pr. Angot, F-64053 Pau, France.

出版信息

Anal Chim Acta. 2015 Jan 15;855:13-20. doi: 10.1016/j.aca.2014.12.010. Epub 2014 Dec 10.

Abstract

This text presents a novel method for the separation and detection of phosphorothioate oligonucleotides with the use of ion pair ultra high performance liquid chromatography coupled with inductively coupled plasma mass spectrometry The research showed that hexafluoroisopropanol/triethylamine based mobile phases may be successfully used when liquid chromatography is coupled with such elemental detection. However, the concentration of both HFIP and TEA influences the final result. The lower concentration of HFIP, the lower the background in ICP-MS and the greater the sensitivity. The method applied for the analysis of serum samples was based on high resolution inductively coupled plasma mass spectrometry. Utilization of this method allows determination of fifty times lower quantity of phosphorothioate oligonucleotides than in the case of quadrupole mass analyzer. Monitoring of (31)P may be used to quantify these compounds at the level of 80 μg L(-1), while simultaneous determination of sulfur is very useful for qualitative analysis. Moreover, the results presented in this paper demonstrate the practical applicability of coupling LC with ICP-MS in determining phosphorothioate oligonucleotides and their metabolites in serum within 7 min with a very good sensitivity. The method was linear in the concentration range between 0.2 and 3 mg L(-1). The limit of detection was in the range of 0.07 and 0.13 mg L(-1). Accuracy varied with concentration, but was in the range of 3%.

摘要

本文介绍了一种采用离子对超高效液相色谱与电感耦合等离子体质谱联用技术分离和检测硫代磷酸酯寡核苷酸的新方法。研究表明,当液相色谱与这种元素检测技术联用时,基于六氟异丙醇/三乙胺的流动相可成功使用。然而,六氟异丙醇和三乙胺的浓度都会影响最终结果。六氟异丙醇浓度越低,电感耦合等离子体质谱中的背景越低,灵敏度越高。用于血清样品分析的方法基于高分辨率电感耦合等离子体质谱。与四极杆质谱分析仪相比,使用该方法可测定低50倍量的硫代磷酸酯寡核苷酸。监测³¹P可用于在80 μg L⁻¹水平上对这些化合物进行定量,同时测定硫对定性分析非常有用。此外,本文给出的结果证明了液相色谱与电感耦合等离子体质谱联用在7分钟内测定血清中硫代磷酸酯寡核苷酸及其代谢物方面具有实际适用性,灵敏度非常好。该方法在0.2至3 mg L⁻¹的浓度范围内呈线性。检测限在0.07至0.13 mg L⁻¹范围内。准确度随浓度而变化,但在3%范围内。

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