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评价在高压下运行的填充亚 2µm 颗粒的水相体积排阻色谱柱的颗粒和床层完整性。

Evaluation of particle and bed integrity of aqueous size-exclusion columns packed with sub-2 µm particles operated at high pressure.

机构信息

Vrije Universiteit Brussel (VUB), Department of Chemical Engineering, Pleinlaan 2, B-1050, Brussels, Belgium.

Vrije Universiteit Brussel (VUB), Department of Chemical Engineering, Pleinlaan 2, B-1050, Brussels, Belgium.

出版信息

J Chromatogr A. 2020 Jun 21;1621:461064. doi: 10.1016/j.chroma.2020.461064. Epub 2020 Apr 11.

DOI:10.1016/j.chroma.2020.461064
PMID:32336499
Abstract

The performance of columns packed with 1.7 µm particles for aqueous size-exclusion chromatography was assessed at high-pressure conditions and linked to particle- and column-bed integrity. Decreasing the particle size from 3.5 µm to 1.7 µm increases the resolution due to the improved mass-transfer characteristics, allowing to significantly speed-up analysis without compromising the selectivity. A sub-minute separation of intact proteins was realized on a 4.6 mm i.d × 75 mm long column packed with 1.7 µm SEC particles applying a flow rate of 1.8 mL/min, corresponding to a column pressure of 530 bar. Ultra-high pressure operation (exceeding manufacturer's recommendations) resulted in peak deformation, a shift towards earlier retention times, and an alteration in selectivity. To gain insights in the mechanisms of column deterioration, short 30 mm long columns were operated at UHPLC conditions, maximizing the pressure drop over individual particles. This resulted in the presence of fractured particles situated at the column outlet, as verified by scanning electron micrographs. Mercury-intrusion porosimetry and argon-adsorption measurements did not reveal significant differences in intraparticle volume between particle batches sampled before and after pressure stress testing. As particles at the column outlet fracture (but not collapse) at high pressure operation, a void was formed at the column inlet. The degradation of the separation performance appeared to be the result of a decrease in interparticle pore volume.

摘要

在高压条件下评估了填充 1.7μm 颗粒的色谱柱在水相尺寸排阻色谱中的性能,并将其与颗粒和柱床完整性联系起来。将粒径从 3.5μm 减小到 1.7μm 会由于改进的传质特性而提高分辨率,从而能够在不影响选择性的情况下显著加快分析速度。在 4.6mm ID×75mm 长的色谱柱上,采用 1.8mL/min 的流速(相当于 530bar 的柱压),填充 1.7μm SEC 颗粒,可实现完整蛋白质的亚分钟分离。超高压力操作(超过制造商的建议)会导致峰变形、保留时间提前以及选择性改变。为了深入了解柱恶化的机制,在超高效液相色谱条件下运行短的 30mm 长柱,使单个颗粒上的压降最大化。这导致在柱出口处存在断裂的颗粒,这通过扫描电子显微镜图像得到了验证。汞侵入孔隙率和氩吸附测量没有显示出在压力应力测试前后采样的颗粒批次之间的颗粒内体积有显著差异。由于在高压操作下,柱出口处的颗粒会断裂(但不会塌陷),因此在柱入口处形成了一个空隙。分离性能的退化似乎是由于颗粒间孔体积的减少所致。

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