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Modeling the drug release from ionic and covalent co-cross-linked chitosan hydrogels

机译:从离子和共价联合壳聚糖水凝胶中造型药物释放

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We propose a model for drug release from co-cross-linked chitosan hydrogels undergoing by surface erosion. The matrix degradation is modeled as an empirical nth order reaction, and the drug release occurs due to diffusion combined with surface erosion. The erosion is described by a moving front represented by a coordinate transformation method. The model reformulated after scaling is fitted to experimental data using the least squares criterion where the Dynamic Optimization problem enclosing the model is solved applying a sequential algorithm. In this study we consider the diffusion of cisplatin in co-cross-linked chitosan hydrogels where the cross-linkers are glycerol phosphate disodium salt and genipin. The release medium is phosphate-buffered saline (PBS) with lysozyme in concentrations similar to those available in human serum. The increase of cross-linker load reduces the diffusion rate, and increases the amount of drug retained in the matrix.
机译:我们提出了一种由遭受表面侵蚀的共交联壳聚糖水凝胶的药物释放模型。基质降解被建模为经验性第n阶反应,并且由于扩散与表面腐蚀结合而发生药物释放。通过由坐标变换方法表示的移动前部描述侵蚀。在缩放后重新制定的模型适用于使用最小二乘标准的实验数据,其中求解封闭模型的动态优化问题,应用顺序算法。在这项研究中,我们认为顺铂在共传送的壳聚糖水凝胶中的扩散,其中交联剂是甘油磷酸二钠盐和Genipin。释放培养基是磷酸盐缓冲盐水(PBS),其浓度与人血清中可用的浓度相似。交联剂负荷的增加降低了扩散速率,并增加了在基质中保留的药物量。

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