Departamento de Investigación en Polímeros y Materiales, Universidad de Sonora, Blvd. Luis Encinas y Rosales S/N, Col. Centro, Hermosillo, Sonora, CP 83000, Mexico.
Departamento de Química, Facultad de Ciencias, Universidad de Navarra, C/Irunlarrea s/n, Pamplona 31080, Navarra, Spain.
Carbohydr Polym. 2018 Sep 1;195:476-485. doi: 10.1016/j.carbpol.2018.05.004. Epub 2018 May 2.
The freezing-thawing is an advantageous method to produce hydrogels without crosslinking agents. In this study chitosan-poly(vinyl alcohol) (CS-PVA) hydrogels were prepared by varying the freezing conditions and composition, which affect the final characteristics of the products. The swelling degree, morphology, porosity, and diflunisal drug loading, as well as the drug release profiles were evaluated. The hydrogel swelling ratio was found to be mainly affected by the CS content, the number of freezing cycles and the temperature. SEM micrographs and porosity data confirm that pore size increases with the chitosan content. However, the use of either lower temperatures or longer freezing times, results in higher porosity and smaller pores. The drug release times of the CS-PVA hydrogels were as long as 30 h, and according to the mathematical fitting, a simple diffusion mechanism dominates the process. Moreover, a mathematical model predicting the hydrogels physical and structural behavior is proposed.
冻融法是一种不使用交联剂制备水凝胶的有利方法。在这项研究中,通过改变冷冻条件和组成制备壳聚糖-聚乙烯醇(CS-PVA)水凝胶,这会影响产品的最终特性。评估了溶胀度、形态、孔隙率、双氯芬酸钠药物负载以及药物释放曲线。发现水凝胶的溶胀比主要受 CS 含量、冷冻循环次数和温度的影响。SEM 显微照片和孔隙率数据证实,随着壳聚糖含量的增加,孔径增大。然而,使用较低的温度或较长的冷冻时间会导致更高的孔隙率和更小的孔。CS-PVA 水凝胶的药物释放时间长达 30 小时,根据数学拟合,简单扩散机制主导了该过程。此外,还提出了一个预测水凝胶物理和结构行为的数学模型。