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Investigation of the adsorption of PEG1500-12-acyloxystearate surfactants onto phospholipid bilayers: An ellipsometry and Cryo-TEM study

机译:PEG1500-12-酰氧基硬脂酸酯表面活性剂在磷脂双层膜上的吸附研究:椭圆偏振法和低温TEM研究

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摘要

In this article we present a study of a new class of surfactants denoted as PEG1500-12-acyloxystearates, which have potential use as pharmaceutical solubilizers. These amphiphilic molecules present interesting properties with regard to cell damage effects. PEG1500-12-acyloxystearates with C-14 to C-16 acyloxy chains cause little or no damage to red blood and intestinal cells, whereas the surfactants with shorter chains, from C-8 to C-12, induce measurable damage. To start unraveling the reason why there is this rather marked dependence of the cell damage effect on surfactant chain length, we have carried out systematic studies of adsorption properties of the surfactants onto phospholipid bilayers by means of ellipsometry. The rate of incorporation of the surfactants in the lipid membrane decreases with increasing length of the acyloxy chain. Cryo-TEM images strengthen the ellipsometry results by showing that the dissolution of the phospholipid bilayer is slower for the surfactants of the series having longer chains.
机译:在本文中,我们对一类新的表面活性剂(称为PEG1500-12-酰氧基硬脂酸酯)进行了研究,该表面活性剂具有潜在的药物增溶剂用途。这些两亲分子在细胞损伤作用方面表现出令人感兴趣的性质。具有C-14至C-16酰氧基链的PEG1500-12-酰氧基硬脂酸酯对红血球和肠道细胞几乎没有或没有造成损害,而从C-8到C-12的较短链的表面活性剂则引起可测量的损害。为了弄清为什么细胞损伤作用对表面活性剂链长有这种相当显着的依赖性,我们已经通过椭偏法系统研究了表面活性剂在磷脂双层上的吸附性能。表面活性剂在脂质膜中的掺入率随酰氧基链长度的增加而降低。通过显示对于具有较长链的系列的表面活性剂,磷脂双层的溶解较慢,冷冻-TEM图像增强了椭圆测定法的结果。

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