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使用大孔球形硅胶作为固定相的多糖的尺寸排阻色谱分离法

SEC Separation of Polysaccharides Using Macroporous Spherical Silica Gel as a Stationary Phase.

作者信息

Krawczyk Tomasz, Zalewski Mariusz, Janeta Anna, Hodurek Paweł

机构信息

1Department of Chemical Organic Technology and Petrochemistry, Faculty of Chemistry, Silesian University of Technology, ul. Krzywoustego 4, 44-100 Gliwice, Poland.

2Wroclaw Medical University, Wybrzeże L. Pasteura 1, 50-367 Wrocław, Poland.

出版信息

Chromatographia. 2018;81(10):1365-1372. doi: 10.1007/s10337-018-3582-5. Epub 2018 Aug 6.

DOI:10.1007/s10337-018-3582-5
PMID:30294004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6153982/
Abstract

ABSTRACT

Meso- and macroporous spherical silica gels of pore sizes in the range of 60-1000 Å and 40-75 µm particle size were investigated as a stationary phase for the separation and purification of polysaccharides and poly(ethylene glycols) (PEGs) of various MWs using an aqueous mobile phase. Sephadex and Bio-Gel were used for comparison as the most common stationary phases for similar purposes. The separation of dextrans of a mean MW = 31 kDa from small molecules (NaCl) was possible with SiO with a pore size of 60-300 Å, but the observed efficiencies of a column of the same size were lower comparing with Sephadex or Bio-Gel. In the case of oxidized alginic acid only SiO of the 60 Å pore size was suitable, while Sephadex, Bio-Gel and other investigated silicas were not efficient. Sephadex and 300-1000 Å SiO offered the possibility of dividing dextrans with MW within the range of 1 MDa-10 kDa into fractions of various MWs, while Bio-Gel and 60 Å SiO were not suitable. The investigated silica gels strongly adsorbed PEGs of MW 2-20 kDa. The amount adsorbed decreased with the increase of pore size and they were not useful as a stationary phase for this class of polymers. An advantage of SiO of the investigated particle size was a very low back pressure comparing with Sephadex. A considerably lower price of silica offers time- and cost-efficient separation of polysaccharides.

摘要

摘要

研究了孔径在60 - 1000 Å范围内、粒径为40 - 75 µm的中孔和大孔球形硅胶作为固定相,用于使用水性流动相分离和纯化各种分子量的多糖和聚乙二醇(PEG)。使用葡聚糖凝胶(Sephadex)和生物凝胶(Bio - Gel)作为类似用途最常用的固定相进行比较。对于平均分子量为31 kDa的右旋糖酐与小分子(氯化钠)的分离,孔径为60 - 300 Å的硅胶是可行的,但与葡聚糖凝胶或生物凝胶相比,相同尺寸柱的观察效率较低。对于氧化海藻酸,只有孔径为60 Å的硅胶适用,而葡聚糖凝胶、生物凝胶和其他研究的硅胶效率不高。葡聚糖凝胶和孔径为300 - 1000 Å的硅胶能够将分子量在1 MDa - 10 kDa范围内的右旋糖酐分成不同分子量的级分,而生物凝胶和孔径为60 Å的硅胶不适用。所研究的硅胶强烈吸附分子量为2 - 20 kDa的PEG。吸附量随孔径增加而降低,它们不适用于这类聚合物的固定相。所研究粒径的硅胶的一个优点是与葡聚糖凝胶相比背压非常低。硅胶价格低得多,可实现多糖的高效且经济的分离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/40438d545ad6/10337_2018_3582_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/08904f7a9467/10337_2018_3582_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/6f0951686134/10337_2018_3582_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/2038a87ae367/10337_2018_3582_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/f67d2868e0ff/10337_2018_3582_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/2d9de9ead0ea/10337_2018_3582_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/40438d545ad6/10337_2018_3582_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/08904f7a9467/10337_2018_3582_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/6f0951686134/10337_2018_3582_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/2038a87ae367/10337_2018_3582_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/f67d2868e0ff/10337_2018_3582_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/2d9de9ead0ea/10337_2018_3582_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0332/6153982/40438d545ad6/10337_2018_3582_Fig6_HTML.jpg

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