Avila-Salas Fabián, Rodriguez Nuñez Yeray A, Marican Adolfo, Castro Ricardo I, Villaseñor Jorge, Santos Leonardo S, Wehinger Sergio, Durán-Lara Esteban F
Centro de Nanotecnología Aplicada, Facultad de Ciencias, Universidad Mayor, Huechuraba 8580000, Región Metropolitana, Chile.
BioNanoMaterials Lab|Drug Delivery and Controlled Release, Universidad de Talca, Talca 3460000, Maule, Chile.
Polymers (Basel). 2018 Jul 23;10(7):806. doi: 10.3390/polym10070806.
This work depicts the rational development (in-silico design, synthesis, characterization and in-vitro evaluation) of polyvinyl alcohol hydrogels (PVAH) cross-linked with maleic acid (MA) and linked to γ-cyclodextrin molecules (γ-CDPVAHMA) as systems for the controlled and sustained release of nifedipine (NFD). Through computational studies, the structural blocks (PVA chain + dicarboxylic acid + γ-CD) of 20 different hydrogels were evaluated to test their interaction energies (Δ) with NFD. According to the Δ obtained, the hydrogel cross-linked with maleic acid was selected. To characterize the intermolecular interactions between NFD and γ-CDPVAHMA, molecular dynamics simulation studies were carried out. Experimentally, three hydrogel formulations with different proportions of γ-CD (2.43%, 3.61% and 4.76%) were synthesized and characterized. Both loading and release of NFD from the hydrogels were evaluated at acid and basic pH. The computational and experimental results show that γ-CDs linked to the hydrogels were able to form 1:1 inclusion complexes with NFD molecules. Finally, γ-CDPVAHMA-3 demonstrated to be the best pH-sensitive release platform for nifedipine. Its effectiveness could significantly reduce the adverse effects caused by the anticipated release of NFD in the stomach of patients.
这项工作描述了用马来酸(MA)交联并与γ-环糊精分子相连的聚乙烯醇水凝胶(PVAH,即γ-CDPVAHMA)作为硝苯地平(NFD)控释和缓释系统的合理开发(计算机辅助设计、合成、表征及体外评估)。通过计算研究,评估了20种不同水凝胶的结构单元(PVA链+二元羧酸+γ-CD)与NFD的相互作用能(Δ)。根据所得的Δ,选择了用马来酸交联的水凝胶。为了表征NFD与γ-CDPVAHMA之间的分子间相互作用,进行了分子动力学模拟研究。通过实验,合成并表征了三种不同γ-CD比例(2.43%、3.61%和4.76%)的水凝胶配方。在酸性和碱性pH条件下评估了NFD从水凝胶中的负载和释放情况。计算和实验结果表明,与水凝胶相连的γ-CD能够与NFD分子形成1:1的包合物。最后,γ-CDPVAHMA-3被证明是硝苯地平最佳的pH敏感释放平台。其有效性可显著降低患者胃部NFD预期释放所引起的不良反应。