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具有径向取向孔和定制孔径的 1.9μm 表面多孔填充材料,用于超快速分离小分子和生物分子。

1.9 μm superficially porous packing material with radially oriented pores and tailored pore size for ultra-fast separation of small molecules and biomolecules.

机构信息

National Chromatographic R. & A. Center, Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China; University of Chinese Academy of Sciences, Beijing 100039, China.

National Chromatographic R. & A. Center, Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

出版信息

J Chromatogr A. 2014 Aug 22;1356:148-56. doi: 10.1016/j.chroma.2014.06.049. Epub 2014 Jun 21.

Abstract

In this work, 1.9 μm reversed-phase packing materials with superficially porous structure were prepared to achieve the rapid and high efficient separation of peptides and proteins. The silica particles were synthesized via three steps, nonporous silica particle preparation by a modified seeded growth method, mesoporous shell formation by a one pot templated dissolution and redeposition strategy, and pore size expansion via acid-refluxing. By such a method, 1.9 μm superficially porous materials with 0.18 μm shell thickness and tailored pore diameter (10 nm, 15 nm) were obtained. After pore enlargement, the formerly dense arrays of mesoporous structure changed, the radially oriented pores dominated the superficially porous structure. The chromatographic performance of such particles was investigated after C18 derivatization. For packing materials with 1.9 μm diameter and 10 nm pore size, the column efficiency could reach 211,300 plates per m for naphthalene. To achieve the high resolution separation of peptides and proteins, particles with pore diameter of 15 nm were tailored, by which the baseline separation of 5 peptides and 5 intact proteins could be respectively achieved within 1 min, demonstrating the superiority in the high efficiency and high throughput analysis of biomolecules. Furthermore, BSA digests were well separated with peak capacity of 120 in 30 min on a 15 cm-long column. Finally, we compared our columns with a 1.7 μm Kinetex C18 column under the same conditions, our particles with 10nm pore size demonstrated similar performance for separation of the large intact proteins. Moreover, the particles with 15 nm pore size showed more symmetrical peaks for the separation of large proteins (BSA, OVA and IgG) and provided rapid separation of protein extracts from Escherichia coli in 5 min. All these results indicated that the synthesized 1.9 μm superficially porous silica packing materials would be promising in the ultra-fast and high-resolution separation of biomolecules.

摘要

在这项工作中,制备了具有反相表面多孔结构的 1.9μm 反相填充材料,以实现肽和蛋白质的快速高效分离。通过三步法合成了硅胶粒子,采用改进的种子生长法制备无孔硅胶粒子,通过一锅模板溶解和再沉淀策略形成介孔壳,然后通过酸回流进行孔径扩大。采用这种方法,获得了 1.9μm 的具有 0.18μm 壳厚和定制孔径(10nm、15nm)的表面多孔材料。孔径扩大后,以前密集排列的介孔结构发生变化,径向取向的孔主导了表面多孔结构。对经过 C18 衍生化后的这些颗粒的色谱性能进行了研究。对于直径为 1.9μm、孔径为 10nm 的填充材料,萘的柱效可达到 211,300 板/米。为了实现肽和蛋白质的高分辨率分离,定制了孔径为 15nm 的颗粒,通过这些颗粒可在 1 分钟内分别实现 5 种肽和 5 种完整蛋白质的基线分离,证明了在生物分子的高效和高通量分析方面具有优越性。此外,在 30 分钟内,在 15cm 长的柱子上可以实现 BSA 消化物的良好分离,峰容量为 120。最后,我们在相同条件下将我们的柱子与 1.7μm Kinetex C18 柱子进行了比较,结果表明,我们的 10nm 孔径颗粒在分离大的完整蛋白质方面具有相似的性能。此外,对于大蛋白质(BSA、OVA 和 IgG)的分离,15nm 孔径的颗粒显示出更对称的峰,并且可以在 5 分钟内从大肠杆菌中快速分离蛋白质提取物。所有这些结果表明,合成的 1.9μm 表面多孔硅胶填充材料有望在生物分子的超快速和高分辨率分离中发挥重要作用。

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