Department of Chemistry, Center for Self-Assembled Chemical Structures (CSACS), Université de Montréal, C.P. 6128, Succursale Centre-Ville, Montréal, QC, Canada H3C 3J7.
J Colloid Interface Sci. 2011 May 15;357(2):419-27. doi: 10.1016/j.jcis.2011.02.033. Epub 2011 Feb 17.
Curdlan, a bacterial polysaccharide, can form different types of thermogels, having the very same chemical composition, but whose structures depend on the incubation temperature. Structural characterization of 10% (w/v) low-set and high-set curdlan gels was carried out by Fourier transformed infrared (FT-IR) imaging and environmental scanning electron microscopy (eSEM) in the hydrated state. Considerable differences were observed between the two gels, the high-set one being overall more homogeneous. The self-diffusion coefficients of a series of analytes of different sizes (water, phosphate, glucose-6-phosphate, polyphosphate, polyethylene glycol, and dextran labelled with rhodamine B) were measured in aqueous solution (D(s)(sln)) and in both types of curdlan gels (D(s)(gel)) using (1)H and (31)P pulsed field gradient nuclear magnetic resonance (PFG NMR) spectroscopy. The mutual-diffusion coefficients (D(m)(gel)) of dextran in the curdlan gels were determined from release experiments based on fluorescence spectroscopy. The dependence of the relative diffusion coefficient (D(s)(gel)D(s)(sln)) on the size of the analyte, expressed by its hydrodynamic radius (R(h)), could be expressed by D(s)(gel)D(s)(sln) ∝ exp(-R(h)(0.46)), valid for both types of gels. The self-diffusion measurements for the largest investigated analytes were not compatible with a single diffusion coefficient and, therefore, were analysed using an approach based on a normal distribution of self-diffusion coefficients. In the hydrogels, broadening of the self-diffusion coefficient distribution increased as a function of the analyte size. This phenomenon was associated with the limited distance travelled by the analytes during the measurements, and it is inferred that the distribution of diffusion coefficients is representative of the distribution of local environments of the individual analyte. It was found that the structural differences observed between both types of curdlan gels are not correlated with the gel transport properties, highlighting the complexity of the relationship between structural details and transport properties in gels.
凝乳多糖是一种细菌多糖,可以形成不同类型的热凝胶,它们具有相同的化学组成,但结构取决于孵育温度。通过傅里叶变换红外(FT-IR)成像和环境扫描电子显微镜(eSEM)对 10%(w/v)低设定和高设定凝乳多糖凝胶的结构进行了表征,在水合状态下进行。观察到两种凝胶之间存在显著差异,高设定凝胶整体更均匀。使用(1)H 和(31)P 脉冲场梯度核磁共振(PFG NMR)光谱法,在水溶液(D(sln))和两种类型的凝乳多糖凝胶(D(gel))中测量了一系列不同大小的分析物(水、磷酸盐、葡萄糖-6-磷酸、多磷酸盐、聚乙二醇和用罗丹明 B 标记的葡聚糖)的自扩散系数。基于荧光光谱法,从释放实验中确定了葡聚糖在凝乳多糖凝胶中的互扩散系数(D(gel))。相对扩散系数(D(gel)D(sln))对分析物尺寸的依赖性,用其水动力半径(R(h))表示,可以表示为 D(gel)D(sln)∝exp(-R(h)(0.46)),两种凝胶均适用。对于最大的研究分析物的自扩散测量结果与单个扩散系数不兼容,因此使用基于自扩散系数正态分布的方法进行分析。在水凝胶中,随着分析物尺寸的增加,自扩散系数分布的变宽增加。这种现象与分析物在测量过程中移动的距离有限有关,并且推断扩散系数的分布代表了各个分析物的局部环境的分布。发现两种类型的凝乳多糖凝胶之间观察到的结构差异与凝胶传输性质无关,突出了结构细节与凝胶传输性质之间关系的复杂性。