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制备用于蛋白质吸附的超高孔琼脂糖珠:CaCO3 颗粒含量的影响。

Fabrication of superporous agarose beads for protein adsorption: effect of CaCO3 granules content.

机构信息

Department of Biochemical Engineering and Key Laboratory of Systems Bioengineering of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Weijin Road No. 92, Nankai District, Tianjin 300072, China.

出版信息

J Chromatogr A. 2010 Sep 10;1217(37):5808-16. doi: 10.1016/j.chroma.2010.07.046. Epub 2010 Jul 22.

DOI:10.1016/j.chroma.2010.07.046
PMID:20691973
Abstract

Agarose gels were fabricated by water-in-oil emulsification with the addition of CaCO(3) granules at 8-16 wt%. Thus agarose beads of different superporosities were produced after dissolving the solid porogen. The superporous agarose (SA) and homogeneous agarose gels were double cross-linked and modified with diethylaminoethyl chloride to produce anion exchangers. We have proposed to use a superporous replica (porous titania microspheres) to examine the superporous structure and pore size distribution of the soft gel. The replica was prepared with the agarose gel entrapping CaCO(3) granules by a sol-gel-templating method. It was found that the superpores created by CaCO(3) granules were uniformly distributed and ranged from 0.95 microm to 1.33 microm. The physical properties of the gels were significantly affected by the porogen content. Importantly, by increasing the solid porogen to 12 wt%, the bed permeability and effective porosity increased about 48% and 33%, respectively. Further increase in the porogen to 16 wt% led to a decrease of the mechanical strength. With increasing superpores in the beads, the dynamic adsorption capacity of the packed columns increased obviously at 305-916 cm/h. Besides, the column efficiency changed less with increasing flow velocity up to 1200 cm/h. It was concluded that the use of 12 wt% CaCO(3) granules in agarose solution was beneficial for the fabrication of the SA gel with good mechanical stability and promising performance for protein chromatography.

摘要

琼脂糖凝胶通过油包水乳液法制备,添加 8-16wt%的碳酸钙颗粒。因此,在溶解固体致孔剂后,得到了具有不同超高孔隙率的琼脂糖珠。超多孔琼脂糖(SA)和均一的琼脂糖凝胶经过双交联和二乙氨基乙基氯修饰,制成阴离子交换剂。我们建议使用超多孔复制体(多孔二氧化钛微球)来检查软凝胶的超多孔结构和孔径分布。复制体是通过溶胶-凝胶模板法用琼脂糖凝胶包埋碳酸钙颗粒制备的。结果发现,碳酸钙颗粒形成的超孔均匀分布,孔径范围为 0.95 微米至 1.33 微米。致孔剂含量显著影响凝胶的物理性质。重要的是,通过将固体致孔剂增加到 12wt%,床层渗透率和有效孔隙率分别增加了约 48%和 33%。进一步增加致孔剂至 16wt%会导致机械强度降低。随着珠内超孔的增加,填充柱的动态吸附容量明显增加,达到 305-916cm/h。此外,在流速增加到 1200cm/h 时,柱效率变化不大。因此,在琼脂糖溶液中使用 12wt%的碳酸钙颗粒有利于制备具有良好机械稳定性和蛋白质色谱性能的 SA 凝胶。

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