Rossi S, Ferrari F, Bonferoni M C, Caramella C
Department of Pharmaceutical Chemistry, University of Pavia, V.le Taramelli, 12, 27100 Pavia, Italy.
Eur J Pharm Sci. 2001 Feb;12(4):479-85. doi: 10.1016/s0928-0987(00)00194-9.
The aim of the present work was to investigate the influence of polymer concentration and polymer:mucin weight ratio on chitosan--mucin interaction, assessed by means of viscosimetric measurements. Two hydration media, distilled water and 0.1 M HCl, were used. Chitosan solutions were prepared at concentrations greater than the characteristic entanglement concentration and mixed with increasing amounts of porcine gastric mucin. Viscosity measurements were performed on the polymer--mucin mixtures and on polymer and mucin solutions having the same concentrations as in the mixtures. The flow curves were fitted according to a modified form of Cheng--Evans equation in order to obtain the relevant model parameters: low shear viscosity eta(0) and high shear viscosity eta(infinity), indexes of the sample structure at rest and upon high shear, respectively. The formation of chitosan--mucin interaction products was determined on the basis of the changes in eta(0) and eta(infinity) of the mixtures as a function of polymer:mucin weight ratio. Rheological synergism parameter was also calculated. The results obtained suggest that two different types of rheological interaction occur between chitosan and mucin in both media, depending on polymer concentration and polymer:mucin weight ratio: one is characterized by a minimum in viscosity and occurs at higher polymer:mucin weight ratio, the other one produces a positive rheological synergism and is observed in presence of an excess of mucin. Only the last one causes a 'strengthening' of the mucoadhesive interface and it is responsible for the mucoadhesive joint. This hypothesis is confirmed by tensile stress measurements performed on HCS solutions in presence of mucin dispersions at different concentrations.
本研究的目的是通过粘度测量来研究聚合物浓度和聚合物与粘蛋白的重量比对壳聚糖与粘蛋白相互作用的影响。使用了两种水合介质,即蒸馏水和0.1M盐酸。制备了浓度高于特征缠结浓度的壳聚糖溶液,并与越来越多的猪胃粘蛋白混合。对聚合物-粘蛋白混合物以及与混合物浓度相同的聚合物和粘蛋白溶液进行粘度测量。根据Cheng-Evans方程的修正形式拟合流动曲线,以获得相关模型参数:低剪切粘度η(0)和高剪切粘度η(∞),分别为样品静止时和高剪切时结构的指标。根据混合物的η(0)和η(∞)随聚合物与粘蛋白重量比的变化来确定壳聚糖-粘蛋白相互作用产物的形成。还计算了流变协同参数。所得结果表明,在两种介质中,壳聚糖和粘蛋白之间存在两种不同类型的流变相互作用,这取决于聚合物浓度和聚合物与粘蛋白的重量比:一种以粘度最小值为特征,发生在较高的聚合物与粘蛋白重量比时,另一种产生正的流变协同作用,在粘蛋白过量时观察到。只有最后一种会导致粘膜粘附界面的“强化”,并负责粘膜粘附连接。在不同浓度的粘蛋白分散体存在下对壳聚糖溶液进行拉伸应力测量,证实了这一假设。