Guarnizo-Herrero Víctor, Torrado-Salmerón Carlos, Torres Pabón Norma Sofía, Torrado Durán Guillermo, Morales Javier, Torrado-Santiago Santiago
Department of Pharmaceutics and Food Technology, Faculty of Pharmacy, Complutense University, Plaza Ramón y Cajal s/n, 28040 Madrid, Spain.
Department of Biomedical Science, Faculty of Pharmacy, University of Alcalá de Henares, Ctra Madrid-Barcelona Km 33,600, 28805 Madrid, Spain.
Polymers (Basel). 2021 Aug 21;13(16):2813. doi: 10.3390/polym13162813.
This study investigated the combination of different proportions of cationic chitosan and anionic carboxymethyl cellulose (CMC) for the development of polyelectrolyte complexes to be used as a carrier in a sustained-release system. Analysis via scanning electron microscopy (SEM) Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and powder X-ray diffraction (PXRD) confirmed ionic interactions occur between the chitosan and carboxymethyl cellulose chains, which increases drug entrapment. The results of the dissolution study in acetate buffer (pH 4.2) showed significant increases in the kinetic profiles of clarithromycin for low proportions of chitosan/carboxymethyl cellulose tablets, while the tablets containing only chitosan had high relaxation of chitosan chains and disintegrated rapidly. The Korsmeyer-Peppas kinetic model for the different interpolymer complexes demonstrated that the clarithromycin transport mechanism was controlled by Fickian diffusion. These results suggest that the matrix tablets with different proportions of chitosan/carboxymethyl cellulose enhanced the ionic interaction and enabled the prolonged release of clarithromycin.
本研究考察了不同比例的阳离子壳聚糖与阴离子羧甲基纤维素(CMC)组合用于开发聚电解质复合物,以作为缓释系统中的载体。通过扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)和粉末X射线衍射(PXRD)分析证实壳聚糖与羧甲基纤维素链之间发生了离子相互作用,这增加了药物包封率。在醋酸盐缓冲液(pH 4.2)中的溶出度研究结果表明,低比例壳聚糖/羧甲基纤维素片剂的克拉霉素动力学曲线有显著增加,而仅含壳聚糖的片剂壳聚糖链松弛度高且迅速崩解。不同聚合物间复合物的Korsmeyer-Peppas动力学模型表明,克拉霉素的转运机制受菲克扩散控制。这些结果表明,不同比例壳聚糖/羧甲基纤维素的基质片剂增强了离子相互作用,并实现了克拉霉素的长效释放。