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用于在线固相萃取毛细管电泳预富集肽段的开放管状C18硅胶整体微柱的制备与评价

Preparation and evaluation of open tubular C18-silica monolithic microcartridges for preconcentration of peptides by on-line solid phase extraction capillary electrophoresis.

作者信息

Ortiz-Villanueva Elena, Benavente Fernando, Giménez Estela, Yilmaz Fatma, Sanz-Nebot Victoria

机构信息

Department of Analytical Chemistry, University of Barcelona, Diagonal 645, 08028 Barcelona, Spain.

Department of Analytical Chemistry, University of Barcelona, Diagonal 645, 08028 Barcelona, Spain.

出版信息

Anal Chim Acta. 2014 Oct 10;846:51-9. doi: 10.1016/j.aca.2014.06.046. Epub 2014 Jun 28.

Abstract

In this study, C18-silica monoliths were synthesized as a porous layer in open tubular capillary columns, to be cut later into microcartridges for the analysis of neuropeptides by on-line solid-phase extraction capillary electrophoresis with UV and MS detection (SPE-CE-UV and SPE-CE-MS). First, several types of C18-silica monolithic (MtC18) microcartridges were used to analyse standard solutions of five neuropeptides (i.e. dynorphin A (1-7), substance P (7-11), endomorphin 1, methionine enkephalin and [Ala]-methionine enkephalin). The MtC18 sorbents were especially selective against endomorphin 1 and substance P (7-11)). The best results in terms of sensitivity and inter-microcartridge reproducibility were achieved with the microcartridges obtained from a 10-cm open tubular capillary column with a thin monolithic coating with large through-pores (1-5μm). Run-to-run repeatability, microcartridge durability, linearity ranges and LODs were studied by MtC18-SPE-CE-MS. As expected due to their greater selectivity, the best LOD enhancement was obtained for End1 and SP (7-11) (50 times with regard to CE-MS). Finally, the suitability of the methodology for analysing biological fluids was tested with plasma samples spiked with End1 and SP (7-11). Results obtained were promising because both neuropeptides could be detected at 0.05μgmL(-1), which was almost the same concentration level as for the standard solutions (0.01μgmL(-1)).

摘要

在本研究中,合成了C18硅胶整体柱作为开口毛细管柱中的多孔层,随后将其切割成微柱,用于通过紫外和质谱检测的在线固相萃取毛细管电泳(SPE-CE-UV和SPE-CE-MS)分析神经肽。首先,使用几种类型的C18硅胶整体柱(MtC18)微柱分析五种神经肽的标准溶液(即强啡肽A(1-7)、P物质(7-11)、内吗啡肽1、甲硫氨酸脑啡肽和[Ala]-甲硫氨酸脑啡肽)。MtC18吸附剂对内吗啡肽1和P物质(7-11)具有特别的选择性。对于从10厘米开口毛细管柱获得的具有大通孔(1-5μm)薄整体涂层的微柱,在灵敏度和微柱间重现性方面取得了最佳结果。通过MtC18-SPE-CE-MS研究了运行间重复性、微柱耐用性、线性范围和检测限。正如预期的那样,由于其更高的选择性,End1和SP(7-11)的检测限提高最为显著(相对于CE-MS提高了50倍)。最后,用添加了End1和SP(7-11)的血浆样品测试了该方法分析生物流体的适用性。获得的结果很有前景,因为两种神经肽在0.05μgmL(-1)时都能被检测到,这几乎与标准溶液(0.01μgmL(-1))的浓度水平相同。

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