Kurdtabar Mehran, Mirashrafi Nazanin-Sadat, Bagheri Marandi Gholam, Ghobadifar Vahid
Department of Chemistry, Karaj Branch, Islamic Azad University, Karaj, Iran.
Department of Chemistry, Karaj Branch, Islamic Azad University, Karaj, Iran.
Int J Biol Macromol. 2024 Nov;281(Pt 4):136532. doi: 10.1016/j.ijbiomac.2024.136532. Epub 2024 Oct 13.
Hydrogels have been widely used in biomedical fields including tissue engineering, drug delivery and cell delivery and 3D cell delivery due to abundant water content in their hydrophilic three-dimensional networks and having soft tissue similar to the human body. In recent years, supramolecular hydrogels (SHG) formed by the inclusion complex between polyethylene glycol (PEG) and macrocycles such as cyclodextrin (CD) have attracted much interest due to their excellent biocompatibility and great potential in biomedical. In this research, a carboxymethyl cellulose (CMC)-based graft copolymer was prepared by using acrylic acid (AA) and maleic anhydride functionalized β-CD (β-CD-MA) as comonomers and ammonium persulfate (APS) as initiator. Then, a self-healable supramolecular hydrogel was synthesized by formation of a host-guest inclusion complex between CMC-g-poly (AA-co-β-CD-MA) as host molecule and cytosine- and guanine-modified PEG as guest molecules. The prepared hydrogel was characterized by Scanning Electron Microscope (SEM), X-Ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Nuclear magnetic resonance spectroscopy (H NMR). The thermal stability of hydrogel was also determined by thermal gravimetric (TGA) and differential scanning calorimetry (DSC) methods. In addition, the loading and release profiles of metformin hydrochloride (MH) drug as a model on hydrogel was investigated. The results indicated that the drug release from the hydrogel peaks around 360 min and aligns with the Ritger-Peppas model. The hydrogel's self-healing property was examined at ambient temperature and 37 °C. It showed 70 % healing in 1.5 h and completed recovery after 9 h.
水凝胶因其亲水性三维网络中含有大量水分且具有与人体相似的软组织,已广泛应用于生物医学领域,包括组织工程、药物递送、细胞递送和三维细胞递送。近年来,由聚乙二醇(PEG)与环糊精(CD)等大环化合物形成的包合物构成的超分子水凝胶(SHG),因其优异的生物相容性和在生物医学方面的巨大潜力而备受关注。在本研究中,以丙烯酸(AA)和马来酸酐功能化的β-环糊精(β-CD-MA)为共聚单体,过硫酸铵(APS)为引发剂,制备了一种基于羧甲基纤维素(CMC)的接枝共聚物。然后,以CMC-g-聚(AA-co-β-CD-MA)为主分子、胞嘧啶和鸟嘌呤修饰的PEG为客体分子,通过形成主客体包合物合成了一种可自愈的超分子水凝胶。通过扫描电子显微镜(SEM)、X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、核磁共振光谱(H NMR)对制备的水凝胶进行了表征。还通过热重分析(TGA)和差示扫描量热法(DSC)测定了水凝胶的热稳定性。此外,研究了作为模型药物的盐酸二甲双胍(MH)在水凝胶上的负载和释放情况。结果表明,水凝胶中药物释放的峰值出现在360分钟左右,符合Ritger-Peppas模型。在室温和37℃下考察了水凝胶的自愈性能。结果表明,该水凝胶在1.5小时内愈合70%,9小时后完全恢复。