David C, Millot M C, Sebille B
Laboratoire de Recherche sur les Polymères, CNRS UMR C7581, Thiais, France.
J Chromatogr B Biomed Sci Appl. 2001 Mar 25;753(1):93-9. doi: 10.1016/s0378-4347(00)00501-6.
The formation of inclusion complexes between polyethylene glycols (PEGs) bearing hydrophobic ends (naphtyl and phenyladamantyl) and beta-cyclodextrin polymers (poly beta-CD) immobilized onto silica particles was studied by high-performance liquid chromatography (HPLC). It was shown that hydrophobic interactions were involved in the retention mechanism of these compounds, since retention volumes decreased when organic solvents were added to the mobile phase while it was the contrary in the presence of salts. Moreover, the association could be reversed by adding a competitor (hydroxypropyl beta-cyclodextrin) to the mobile phase. A theoretical model permitted the evaluation of affinity constants of 1:1 complexes formed between the modified PEGs and the immobilized poly beta-CD which depended on the type of hydrophobic groups grafted to the PEG.
通过高效液相色谱法(HPLC)研究了带有疏水端(萘基和苯基金刚烷基)的聚乙二醇(PEG)与固定在硅胶颗粒上的β-环糊精聚合物(聚β-环糊精)之间包合物的形成。结果表明,这些化合物的保留机制涉及疏水相互作用,因为当向流动相中添加有机溶剂时保留体积减小,而在有盐存在时情况则相反。此外,通过向流动相中添加竞争剂(羟丙基β-环糊精)可以使这种缔合逆转。一个理论模型允许评估改性PEG与固定化聚β-环糊精之间形成的1:1配合物的亲和常数,该常数取决于接枝到PEG上的疏水基团的类型。