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首页> 外文期刊>Analytica chimica acta >Determination of critical micelle concentrations and aggregation numbers by fluorescence correlation spectroscopy: Aggregation of a lipopolysaccharide
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Determination of critical micelle concentrations and aggregation numbers by fluorescence correlation spectroscopy: Aggregation of a lipopolysaccharide

机译:通过荧光相关光谱法确定临界胶束浓度和聚集数:脂多糖的聚集

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Fluorescence correlation spectroscopy(FCS)is often used to determine the mass or radius of a particle by using the dependence of the diffusion coefficient on the mass and shape.In this article we discuss how the particle size of aggregates can be measured by using the concentration dependence of the amplitude of the autocorrelation function(ACF)instead of the temporal decay.We titrate a solution of aggregates or micelles with a fluorescent label that possesses a high affinity for these structures and measure the changes in the amplitude of the ACF.We develop the theory describing the change of the ACF amplitude with increasing concentrations of labels and use it to fit experimental data.It is shown how this method can determine the aggregation number and critical micelle concentration of a standard detergent nonaethylene glycol monododecyl ether(C12E9)and a lipopolysaccharide(LPS: Escherichia coli 0111:B4).
机译:荧光相关光谱法(FCS)通常用于通过确定扩散系数对质量和形状的依赖性来确定颗粒的质量或半径。在本文中,我们讨论了如何通过使用浓度来测量聚集体的粒径我们用自相关函数(ACF)的振幅而不是时间衰减进行依赖。我们用具有对这些结构具有高亲和力的荧光标记滴定聚集体或胶束的溶液,并测量ACF振幅的变化。该理论描述了随着标签浓度的增加ACF振幅的变化并用于实验数据的拟合。表明了该方法如何确定标准去污剂九乙二醇单十二烷基醚(C12E9)的聚集数和临界胶束浓度。脂多糖(LPS:大肠杆菌0111:B4)。

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