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低分子肝素在聚阳离子聚丙烯酰胺基质中的聚焦。

Focusing of low-molecular-mass heparins in polycationic polyacrylamide matrices.

机构信息

Cleardirection Ltd., 4 Pekeris St., Rehovot 76702, Israel.

出版信息

Anal Chem. 2009 Aug 15;81(16):6966-71. doi: 10.1021/ac901050q.

Abstract

A novel method for separation of low-molecular-mass heparins is reported here, on the basis of migrating the polyanionic heparins in a polycationic polyacrylamide gel, made by incorporating a gradient of positively charged monomers (the Immobilines used for creating immobilized pH gradients) into the neutral polyacrylamide backbone. Separations can be operated either in linear or nonlinear gradients of positive charges, thus modulating at whim the separation power. This allows the polydisperse heparins to reach a steady-state position along the migration path and condense (focus) in an environment inducing charge neutralization. It is shown that the separations obtained are a complex function of both size and charge distribution along the oligosaccharide chains. This novel methodology represents a marked improvement over existing techniques and appears to hold promise for applications in screening of commercial lots of heparins, also in view of possible presence of contaminants, such as those recently detected in imported heparins.

摘要

本文报道了一种新型的低分子肝素分离方法,基于在带有正电荷单体梯度的聚阳离子聚丙烯酰胺凝胶中迁移阴离子肝素,该单体梯度是通过将中性聚丙烯酰胺主链中的正电荷单体(用于创建固定 pH 梯度的 Immobilines)进行梯度混合而形成的。分离可以在线性或非线性的正电荷梯度中进行,从而随意调节分离能力。这使得多分散肝素能够在迁移路径上达到稳定状态,并在诱导电荷中和的环境中浓缩(聚焦)。结果表明,所得到的分离是沿着寡糖链的大小和电荷分布的复杂函数。与现有技术相比,这种新方法有了显著的改进,并且似乎有望在筛选肝素的商业批次方面得到应用,同时也考虑到可能存在污染物,如最近在进口肝素中检测到的那些污染物。

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