Dept. of Nutrition and Food Science, Univ. of Maryland, 0112 Skinner Bldg., College Park, MD 20742, USA.
J Food Sci. 2011 Aug;76(6):E472-8. doi: 10.1111/j.1750-3841.2011.02227.x. Epub 2011 Jun 2.
Xanthan-curdlan hydrogel complex (XCHC) has been shown capable of retaining moisture up to 5 freeze-thaw cycles (FTCs); however, moisture distribution in the complex in relation to the hydrogel composition and structure remains uncharacterized. In the present study, magnetic resonance imaging (MRI), nuclear magnetic resonance (NMR) relaxometry, rheology, and scanning electron microscopy (SEM) were used to examine the effect of water distribution and interaction with 2.0% aqueous solutions of xanthan, curdlan, and XCHC consisting of equal amounts of both polysaccharides. A gel structure with an indication of syneresis was clearly seen in the MR image of curdlan alone, whereas the distribution of protons throughout xanthan and XCHC samples remained homogeneous and showed no detectable syneresis. The three-dimensional network, indicated by frequency sweeps, of curdlan was responsible for curdlan's gel structure. The frequency sweep and slope of the storage modulus (G') of XCHC was significantly closer to curdlan with higher elasticity and less dependency upon angular frequency than xanthan alone. The reduction in XCHC dynamic moduli (G' and G″) compared to curdlan could be attributed to the formation of wavy layers instead of a fully cured three-dimensional structure. Addition of xanthan to curdlan restricted XCHC spin-spin relaxation time (T₂) to intermediate and slower exchange regimes, namely approximately 110 and 342 ms, respectively, promoting the polymer's interaction with water while inhibiting interpolymer interactions found in curdlan. A 3rd proton pool with the slowest T₂ seen in curdlan was not found in XCHC, correlating to the absence of syneresis.
The combination of texture measurements and discrete noninvasive techniques was found capable of providing insightful understanding of water distribution in a gel system. These techniques may be applied to other hydrogel complexes. The XCHC system investigated has the potential to enhance freeze-thaw stability in frozen food products by minimizing syneresis due to undesirable temperature fluctuations during distribution and consumer application.
已显示黄原胶-卡拉胶水凝胶复合物(XCHC)能够保持水分,直至经过 5 次冻融循环(FTC);然而,复合物中的水分分布与水凝胶的组成和结构仍未被描述。在本研究中,磁共振成像(MRI)、核磁共振(NMR)弛豫率、流变学和扫描电子显微镜(SEM)用于研究水分布的影响以及与 2.0%的黄原胶、卡拉胶和 XCHC 的相互作用,其中 XCHC 由等量的两种多糖组成。单独的卡拉胶的磁共振图像中清楚地显示出凝胶结构,有收缩的迹象,而黄原胶和 XCHC 样品中的质子分布保持均匀,没有可检测到的收缩。由频率扫描表示的卡拉胶的三维网络负责卡拉胶的凝胶结构。XCHC 的频率扫描和储能模量(G')斜率与卡拉胶非常接近,具有更高的弹性,并且比单独的黄原胶对角频率的依赖性更小。与卡拉胶相比,XCHC 动态模量(G'和 G″)的降低可能归因于形成波浪状层而不是完全固化的三维结构。黄原胶添加到卡拉胶中会将 XCHC 的自旋-自旋弛豫时间(T₂)限制在中间和较慢的交换范围,即分别约为 110 和 342ms,从而促进聚合物与水的相互作用,同时抑制卡拉胶中发现的聚合物间相互作用。在 XCHC 中未发现卡拉胶中最慢的 T₂的第三个质子池,这与不存在收缩相关。
纹理测量和离散非侵入技术的组合被发现能够提供对凝胶系统中水分分布的深入了解。这些技术可应用于其他水凝胶复合物。所研究的 XCHC 系统有可能通过最小化由于分配和消费者应用期间的温度波动引起的收缩,来增强冷冻食品的冻融稳定性。