State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China; College of Environment and Chemical Engineering, Yanshan University, Hebei 066000, China.
J Chromatogr A. 2022 Oct 11;1681:463461. doi: 10.1016/j.chroma.2022.463461. Epub 2022 Aug 31.
How to improve the performance of chromatographic media is very important in chromatography. Uniform agarose microspheres were successfully prepared using membrane emulsification method with a controllable particle size, followed by multi-step crosslinking and dextran-grafting, respectively. To obtain both fine pore structure and good pressure-resistant property, the effects of both dextran-grafting and crosslinking process were studied carefully and also, the preparation conditions were delicately adjusted. Inverse size-exclusion chromatography was used for determining the pore structure of these agarose microspheres. Uniform agarose microspheres with an average particle size of about 8 μm were obtained with regularly spherical, transparent and smooth appearance. By introducing a certain molecular weight of dextran or pentaerythritol glycidyl ether at different crosslinking steps, both the pressure-resistant and the chromatographic properties of microspheres were improved. Both the maximum flow velocity and the corresponding pressure drop increased with the decrease of the molecular weight of dextran, i.e., 99 cm/h and 3.22 MPa, respectively, using dextran T3 (3 kDa). The average pore size of agarose microspheres decreased from 6.04±0.56 nm to 2.50±0.12 nm with the increase of the molecular weight of dextran from dextran T3 (3 kDa) to dextran T100 (100 kDa), with a high resolution obtained for a certain molecular range of model proteins. Also, the pressure-resistant property was highly improved in multi-step crosslinking process, with a maximum flow velocity of 107 cm/h and a corresponding pressure drop of 3.62 MPa obtained after the whole crosslinking steps. The average pore size of agarose microspheres was 3.72±0.32, 3.90±0.21 and 3.60±0.27 nm for the introduction of pentaerythritol glycidyl ether as the crosslinking agent at different steps, respectively. These uniform dextran-grafted agarose microspheres have a finely controllable molecular range with a high resolution compared with traditional ones, which are beneficial for chromatographic selectivity. Therefore, they are very useful for high-resolution chromatography and have wide applications in downstream process.
如何提高色谱介质的性能在色谱中非常重要。本文采用膜乳化法成功制备了粒径可控的均一琼脂糖微球,然后分别进行多步交联和葡聚糖接枝。为了获得精细的孔结构和良好的耐压性能,仔细研究了葡聚糖接枝和交联过程的影响,并精心调整了制备条件。反相体积排阻色谱用于测定这些琼脂糖微球的孔结构。通过在不同的交联步骤中引入一定分子量的葡聚糖或季戊四醇缩水甘油醚,可以同时改善微球的耐压性和色谱性能。最大流速和相应的压降均随着葡聚糖分子量的降低而增加,即使用葡聚糖 T3(3 kDa)时分别为 99 cm/h 和 3.22 MPa。琼脂糖微球的平均孔径从 6.04±0.56nm 减小到 2.50±0.12nm,随着葡聚糖分子量从葡聚糖 T3(3 kDa)增加到葡聚糖 T100(100 kDa)而增加,对于特定的分子范围的模型蛋白质获得了高分辨率。此外,在多步交联过程中耐压性能得到了很大的提高,在整个交联步骤后,最大流速为 107cm/h,相应的压降为 3.62MPa。琼脂糖微球的平均孔径分别为 3.72±0.32nm、3.90±0.21nm 和 3.60±0.27nm,在不同步骤中分别使用季戊四醇缩水甘油醚作为交联剂。与传统的琼脂糖微球相比,这些均匀的葡聚糖接枝琼脂糖微球具有精细可控的分子范围和高分辨率,有利于色谱选择性。因此,它们非常适用于高分辨率色谱法,并在下游工艺中有广泛的应用。