Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan, PR China.
J Sep Sci. 2011 Nov;34(22):3123-30. doi: 10.1002/jssc.201100570. Epub 2011 Oct 14.
A novel hydrophilic polymer-coated silica sorbent has been prepared using the radical "grafting from" polymerization method through surface-bound azo initiators for hydrophilic-interaction chromatography (HILIC). The azo groups were introduced to the surface of silica gel through the reaction with amino groups on the surface of silica gel with 4,4'-azobis(4-cyanopentanoic acid chloride) (ACVC). The resultant azo-immobilized silica gel served as surface initiator to polymerize hydrophilic triol acrylamide monomer N-acryloyltris(hydroxymethyl) aminomethane (NA) in methanol to get hydrophilic polymer-coated silica sorbent. The obtained poly(NA)-coated silica (pNA-sil) was characterized by Fourier transform infrared spectroscopy (FT-IR), elemental analysis (EA), and nitrogen sorption porosimetry (NSP). Then the pNA-sil was packed into the stainless-steel column and evaluated in high-performance liquid chromatography (HPLC). Good chromatographic performance for the separation of peptides and nucleosides was obtained under HILIC mode. The results indicated that the pNA-sil stationary phase behaved as mixed-mode retention mechanisms of hydrophilic and ionic interactions. Furthermore, the pNA-sil phase was used to separate tryptic digest of β-casein and our results showed that more than 12 peptides peaks were resolved and well distributed within the elution window. Finally, the pNA-sil stationary phase was demonstrated to possess remarkable reproducibility and stability. Taken together, the pNA-sil stationary phase prepared in the current study offers a potential application in proteomics study.
一种新型亲水聚合物涂覆硅胶固定相,通过表面接枝聚合方法,利用表面结合的偶氮引发剂,用于亲水相互作用色谱(HILIC)。通过与硅胶表面氨基反应,将偶氮基团引入硅胶表面,使用 4,4'-偶氮双(4-氰戊酸)(ACVC)。所得偶氮固定化硅胶作为表面引发剂,在甲醇中聚合亲水三醇丙烯酰胺单体 N-丙烯酰基三(羟甲基)氨基甲烷(NA),得到亲水聚合物涂覆硅胶固定相。所得聚(NA)涂覆硅胶(pNA-sil)通过傅里叶变换红外光谱(FT-IR)、元素分析(EA)和氮气吸附孔隙率(NSP)进行了表征。然后将 pNA-sil 填充到不锈钢柱中,并在高效液相色谱(HPLC)中进行了评价。在 HILIC 模式下,可获得用于分离肽和核苷的良好色谱性能。结果表明,pNA-sil 固定相表现出亲水和离子相互作用的混合保留机制。此外,pNA-sil 相用于分离β-酪蛋白的胰蛋白酶消化物,我们的结果表明,在洗脱窗口内可分离出 12 个以上肽峰,且分布均匀。最后,pNA-sil 固定相表现出良好的重现性和稳定性。综上所述,本研究制备的 pNA-sil 固定相在蛋白质组学研究中具有潜在的应用价值。