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无交联剂时壳聚糖在水溶液中凝胶化的流变学研究

Rheometric study of the gelation of chitosan in aqueous solution without cross-linking agent.

作者信息

Montembault Alexandra, Viton Christophe, Domard Alain

机构信息

Laboratoires Genevrier, 280 rue de Goa, Z.I. Les Trois Moulins, 06901 Sophia-Antipolis, France.

出版信息

Biomacromolecules. 2005 Mar-Apr;6(2):653-62. doi: 10.1021/bm049593m.

Abstract

A new process of formation of chitosan physical hydrogels in aqueous solution, without any organic solvent or cross-linking additive, was studied. The three conditions required for the physical gelation were an initial polymer concentration over C*, a critical value of the balance between hydrophilic and hydrophobic interactions, and a physicochemical perturbation responsible for a bidimensional percolating mechanism. The time necessary to reach the gel point was determined by rheometry, and gelations were compared according to different initial conditions. Thus, we investigated the influence of the polymer concentration and the degree of acetylation (DA) of chitosan on gelation. The number of junctions per unit volume at the gel point varied with the initial polymer concentration, i.e., the initial number of chain entanglements per unit volume or the number of gel precursors. The time to reach the gel point decreased with both higher DAs and concentrations. For a chitosan of DA = 36.7%, a second critical initial concentration close to 1.8% (w/w) was observed. Above this concentration, the decrease of the time to reach the gel point was higher and fewer additional junctions had to be formed to induce gelation. To optimize these physical hydrogels, to be used for cartilage regeneration, their final rheological properties were studied as a function of their degree of acetylation and their polymer concentration. Our results allowed us to define the most appropriate gel for the targeted application corresponding to a final concentration of chitosan in the gel of near 1.5% (w/w) and a DA close to 40%.

摘要

研究了一种在水溶液中形成壳聚糖物理水凝胶的新方法,该方法无需任何有机溶剂或交联添加剂。物理凝胶化所需的三个条件是:初始聚合物浓度超过临界值C*、亲水和疏水相互作用之间平衡的临界值,以及负责二维渗流机制的物理化学扰动。通过流变学测定达到凝胶点所需的时间,并根据不同的初始条件比较凝胶化情况。因此,我们研究了壳聚糖的聚合物浓度和乙酰化程度(DA)对凝胶化的影响。凝胶点处单位体积的连接点数随初始聚合物浓度而变化,即单位体积内链缠结的初始数量或凝胶前体的数量。达到凝胶点的时间随DA和浓度的增加而减少。对于DA = 36.7%的壳聚糖,观察到第二个临界初始浓度接近1.8%(w/w)。高于此浓度,达到凝胶点的时间减少得更多,并且诱导凝胶化所需形成的额外连接点更少。为了优化这些用于软骨再生的物理水凝胶,研究了它们的最终流变性质与乙酰化程度和聚合物浓度的关系。我们的结果使我们能够确定最适合目标应用的凝胶,其对应于凝胶中壳聚糖的最终浓度接近1.5%(w/w)且DA接近40%。

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