Faculty of Chemistry, Khajeh Nasir Toosi University, Tehran, Iran.
Faculty of Chemistry, Shahid Beheshti University, Tehran, Iran.
Int J Biol Macromol. 2021 Jun 30;181:937-944. doi: 10.1016/j.ijbiomac.2021.04.092. Epub 2021 Apr 18.
For stopping long-time harmful bacterial infection, designing a drug carrier with a highly prolonged release profile is a promising approach that is of interest to different biomedical areas. The subject of this work is to synthesis a novel carrier system through coordination of MIL-88(Fe) to carboxymethyl cellulose (CMC) for enhancing interaction between drug and carrier. We established an ultrasound-assisted synthetic method for in situ synthesis of MIL-88(Fe) in the presence of CMC resulting in CMC/MIL-88(Fe) composite. The CMC/MIL-88(Fe) was loaded with a high amount of Tetracycline (TC) by immersion of carrier to the TC aqueous solution. The release profile in the simulated physiological conditions, pH 7.4, revealed a low initial burst release followed by a sustained and prolonged release over 384 h. The in vitro cytotoxicity of CMC/MIL-88(Fe) against Human skin fibroblast (HFF-1) cells was calculated by MTT assay and showed a good cytocompatibility. The antibacterial activity was found for TC-loaded CMC/MIL-88(Fe) toward both E. coli and S. aureus with MIC 64 mg·ml.
为了阻止长期有害细菌感染,设计一种具有高度延长释放特性的药物载体是一种很有前途的方法,引起了不同生物医学领域的关注。本工作的主题是通过 MIL-88(Fe)与羧甲基纤维素(CMC)的配位合成一种新型载体系统,以增强药物与载体之间的相互作用。我们建立了一种超声辅助的原位合成方法,在 CMC 的存在下合成 MIL-88(Fe),得到 CMC/MIL-88(Fe)复合材料。通过将载体浸入四环素(TC)水溶液中,CMC/MIL-88(Fe)可以负载大量的 TC。在模拟生理条件下(pH7.4)的释放曲线显示出低的初始突释,随后是持续和延长的释放超过 384 小时。通过 MTT 测定法计算 CMC/MIL-88(Fe)对人皮肤成纤维细胞(HFF-1)的体外细胞毒性,显示出良好的细胞相容性。发现负载 TC 的 CMC/MIL-88(Fe)对大肠杆菌和金黄色葡萄球菌均具有抗菌活性,MIC 为 64mg·ml。