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采用毛细管电泳-电喷雾电离-质谱联用的固相萃取法鉴定迷迭香蜂蜜中的酚类化合物。

Identification of phenolic compounds in rosemary honey using solid-phase extraction by capillary electrophoresis-electrospray ionization-mass spectrometry.

作者信息

Arráez-Román D, Gómez-Caravaca A M, Gómez-Romero M, Segura-Carretero A, Fernández-Gutiérrez A

机构信息

Department of Analytical Chemistry, Faculty of Sciences, University of Granada, C/Fuentenueva s/n, E-18071 Granada, Spain.

出版信息

J Pharm Biomed Anal. 2006 Aug 28;41(5):1648-56. doi: 10.1016/j.jpba.2006.02.035. Epub 2006 Mar 30.

Abstract

Complex extracts of rosemary honey constituents often require very effective separation techniques to allow the identification of different compounds. Capillary electrophoresis (CE) coupled to mass spectrometry (MS) detection can provide structure-selective information about the analytes in such matrices and has turned out to be an attractive alternative to HPLC methods. A simple and cost-effective analytical method involving solid-phase extraction (SPE) and capillary zone electrophoresis coupled to electrospray ionization-ion trap mass spectrometry (CZE-ESI-MS) to identify and characterize phenolic compounds in rosemary honey is described. The SPE, CE and ESI-MS parameters were optimized in order to maximize the number of phenolic compounds detected and the sensitivity of their determination. All CE-ESI-MS experiments were performed with uncoated fused-silica capillaries and an alkaline volatile buffer system consisting of 100 mM NH(4)Oac with 10% of 2-propanol at pH 10. Since sheath liquids can made significant effects on the sensitivity in typical CE-ESI-MS application, the effect of type and flow rate of the sheath liquid on the sensitivity of phenolic compounds were investigated. As result, the best sensitivity was obtained with a sheath liquid containing 2-propanol/water 60:40 (v/v) and 0.1% (v/v) of triethylamine at 3 microL/min in the negative ion mode. We describe the first method for the analysis of phenolic compounds in rosemary honey at mg/L levels by using a simple SPE before CE-ESI-MS analysis.

摘要

迷迭香蜂蜜成分的复杂提取物通常需要非常有效的分离技术,以鉴定不同的化合物。毛细管电泳(CE)与质谱(MS)检测联用,可以提供有关此类基质中分析物的结构选择性信息,并且已被证明是高效液相色谱(HPLC)方法的一种有吸引力的替代方法。本文描述了一种简单且经济高效的分析方法,该方法涉及固相萃取(SPE)以及毛细管区带电泳与电喷雾电离-离子阱质谱联用(CZE-ESI-MS),用于鉴定和表征迷迭香蜂蜜中的酚类化合物。对SPE、CE和ESI-MS参数进行了优化,以最大限度地提高检测到的酚类化合物数量及其测定的灵敏度。所有CE-ESI-MS实验均使用未涂层的熔融石英毛细管和由100 mM醋酸铵与10%异丙醇组成的碱性挥发性缓冲系统,pH为10。由于鞘液在典型的CE-ESI-MS应用中会对灵敏度产生显著影响,因此研究了鞘液类型和流速对酚类化合物灵敏度的影响。结果表明,在负离子模式下,使用含60:40(v/v)异丙醇/水和0.1%(v/v)三乙胺的鞘液,流速为3 μL/min时,可获得最佳灵敏度。我们描述了第一种在CE-ESI-MS分析前使用简单SPE分析迷迭香蜂蜜中mg/L水平酚类化合物的方法。

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