4.7 Article

Synthesis and optimization of SiO2@SiO2 core-shell microspheres by an improved polymerization-induced colloid aggregation method for fast separation of small solutes and proteins

期刊

TALANTA
卷 207, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2019.120310

关键词

Core-shell silica microsphere; Polymerization-induced colloid aggregation; Urea-formaldehyde polymers; Fast separation; HPLC

资金

  1. National Natural Science Foundation of China of China [21874106, 21545007, 21605122]
  2. Shaanxi Provincial Science and Technology Coordinating Innovation Projects [2013SZS18-K01]
  3. Natural Science Foundation of Shaanxi Province [2018JZ2001, 2018JQ2011]
  4. Foundation of Key Laboratory in Shaanxi Province [2010JS103, 11JS097, 15JS115, 16JS116]

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Recently, superficially porous particles (SPPs) have been intensively studied and employed for highly efficient and fast separations. In this paper, the SiO2@SiO2 SPPs were synthesized by an improved polymerization-induced colloid aggregation (PICA) method using urea-formaldehyde polymer as the template. The agglomeration of silica core during modification with ureidopropyltrimethoxysilane (UPS) can not only be avoided by reflux in neutral ethanol solution, but also the secondary nucleation of the colloidal silica sol can be inhibited via optimizing the reaction conditions including pH, temperature, colloidal silica sol concentration and the reaction time. The shell thickness and pore size of SPPs can be controlled successfully by adjusting the weight ratio of silica core/colloidal silica sol and the particle size of colloidal silica sol, respectively. The SPP-C18 columns packed using octadecyltrichlorosilane (ODS) modified SPPs with different pore sizes were employed to separate small solutes and proteins. The baseline separations of 6 kinds of alkyl benzenes and 5 kinds of aromatic alcohol homologues were achieved within 4?min by the SPP-C18 column with 8?nm pore size. Compared with the commercial BEH-C18 column, more than 50,000/m of the plate number of propylbenzene was obtained, and the former provided higher column efficiency to separate small solutes than the latter. Meanwhile, 6 kinds of proteins were also separated completely within 2?min using the SPP-C18 column with 40?nm pore size. In addition, the SPP-C18 capillary column was applied to separate and identify the BSA/HeLa/mouse liver digests with capillary LC-MSMS, respectively. The results indicate that more proteins and peptides can be identified using SPP-C18 capillary column compared with commercial silica-C18 capillary column. The result demonstrates that the prepared SPP-C18 column provides higher column efficiency and the SPPs synthesized with the improved PICA method shows a great potential application for the fast separation of small solutes and proteins.

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