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基于部分疏水化透明质酸的物理水凝胶中的水动力学。

Water dynamics in physical hydrogels based on partially hydrophobized hyaluronic acid.

机构信息

Dipartimento di Fisica e Scienze della Terra, Università di Parma and CNISM, Parma, Italy.

出版信息

J Phys Chem B. 2012 Nov 1;116(43):12915-21. doi: 10.1021/jp303657a. Epub 2012 Oct 23.

Abstract

The dynamics of hyaluronate-based hydrogels has been investigated by quasielastic neutron scattering (QENS). Hyaluronate (HYA) has been compared, in the same conditions of temperature and polymer concentration, to a chemically modified form, HYADD, in which the backbone has been grafted with a hexadecyl (C(16)) side-chain with a degree of substitution of about 2% (mol/mol). This modification increases the hydrophobicity of the polysaccharide and leads to a stable gel already at polymer concentration of 0.3% (w/v), yielding a viscosupplementation with less quantity of polysaccharide. The time-scale covered by our measurements probes both water and segmental biopolymer motions. In both systems, the local dynamics of the network in the ps time-scale is mostly due to local reorientational motions of side groups. Such motions are not significantly affected by the small amount of aliphatic chains forming the hydrophobic junctions in HYADD. The diffusivity of water in both HYA and HYADD coincides with that of pure water within the experimental uncertainty. This result confirms previous ones on the dynamics of water in HYA solutions and it is of relevance for biomedical applications of hyaluronate-based systems because it affects the diffusive processes of metabolites and their interaction with tissues.

摘要

通过准弹性中子散射(QENS)研究了透明质酸(HYA)基水凝胶的动力学。在相同的温度和聚合物浓度条件下,将透明质酸与化学改性形式 HYADD 进行了比较,其中主链接枝了十六烷基(C(16))侧链,取代度约为 2%(摩尔/摩尔)。这种修饰增加了多糖的疏水性,并导致在聚合物浓度为 0.3%(w/v)时即可形成稳定的凝胶,从而用更少的多糖实现了粘弹性补充。我们测量所涵盖的时间尺度同时探测了水和聚合物链段的运动。在这两种体系中,网络在 ps 时间尺度上的局部动力学主要归因于侧基的局部重取向运动。这些运动受形成 HYADD 中疏水性连接点的少量脂肪链的影响不大。水在 HYA 和 HYADD 中的扩散系数与实验不确定度内的纯水扩散系数一致。这一结果证实了先前关于 HYA 溶液中水分动力学的结果,并且与基于透明质酸的系统的生物医学应用相关,因为它会影响代谢物的扩散过程及其与组织的相互作用。

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