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通过巯基-烯点击反应将聚(3-巯丙基甲基硅氧烷)膜同时功能化和交联到乙烯基硅胶上,得到稳定键合的聚合物反相/弱阴离子交换混合模式固定相。

Stable-bond polymeric reversed-phase/weak anion-exchange mixed-mode stationary phases obtained by simultaneous functionalization and crosslinking of a poly(3-mercaptopropyl)methylsiloxane-film on vinyl silica via thiol-ene double click reaction.

机构信息

Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076 Tübingen, Germany.

Biomembranes Group, Institute of Molecular Science, Universitat de València. C/Catedrático José Beltrán 2, 46980 Paterna, Valencia, Spain.

出版信息

J Chromatogr A. 2019 May 24;1593:110-118. doi: 10.1016/j.chroma.2019.01.078. Epub 2019 Feb 1.

DOI:10.1016/j.chroma.2019.01.078
PMID:30739756
Abstract

A polymeric reversed-phase/weak anion exchange (Poly-RP/WAX) mixed-mode stationary phase has been prepared by coating of a poly(3-mercaptopropyl)methylsiloxane film on vinyl-modified silica (100 Å, 5 μm) and simultaneous in situ functionalization with N-(10-undecenoyl)-3-aminoquinuclidine as well as crosslinking to the vinyl silica surface by solventless thiol-ene double click reaction. Such bonding chemistry showed greatly enhanced stability compared to brush-type analogs with bifunctional siloxane bonding to silica. Solid-state Si-CP/MAS NMR confirmed the immobilization of the siloxane layer. pH-Dependent ζ-potential determinations revealed a high anion-exchange capacity over the entire pH range with a maximum around pH 5. Oxidation of residual thiols yielded a zwitterionic Poly-RP/WAX/SCX mixed-mode phase with sulfonic acid endcapping and shifted the still net positive surface charge to lower ζ-potentials. It allowed a faster elution of strongly retained anionic species in particular of multiply negatively charged analytes such as oligonucleotides. Chromatographic tests under RPLC and HILIC elution mode with various test substances documented the multimodal utility and complementarity in retention profiles compared to RP, HILIC and commercial mixed-mode phases.

摘要

一种聚合型反相/弱阴离子交换(Poly-RP/WAX)混合模式固定相通过在乙烯基改性硅胶(100Å,5μm)上涂覆聚(3-巯丙基)甲基硅氧烷膜,并同时原位功能化 N-(10-十一烯酰基)-3-氨基奎宁环以及通过无溶剂硫醇-烯双点击反应交联到乙烯基硅胶表面来制备。与双官能硅氧烷键合到硅胶的刷型类似物相比,这种键合化学表现出大大增强的稳定性。固态 Si-CP/MAS NMR 证实了硅氧烷层的固定化。pH 值依赖性 ζ-电位测定表明,在整个 pH 范围内具有高的阴离子交换容量,在 pH 5 左右达到最大值。残留硫醇的氧化生成了带有磺酸封端的两性离子 Poly-RP/WAX/SCX 混合模式相,并将仍然带正电荷的表面电荷转移到较低的 ζ-电位。这使得强保留的阴离子物质,特别是多电荷分析物如寡核苷酸,能够更快地洗脱。与 RP、HILIC 和商业混合模式相相比,各种测试物质在 RPLC 和 HILIC 洗脱模式下的色谱测试记录了多模式的实用性和保留谱的互补性。

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引用本文的文献

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