Zheng Heming, An Guanghui, Yang Xiaohui, Huang Lei, Wang Nannan, Zhu Yanqiu
State Key Laboratory of Featured Metal Materials and Life-Cycle Safety for Composite Structures, MOE Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, and School of Resources, Environment and Materials, Guangxi University, Nanning 530004, China.
Department of Radiation Oncology, Guangxi Medical University Cancer Hospital, Cancer Institute of Guangxi Zhuang Autonomous Region, Nanning 530021, China.
Pharmaceuticals (Basel). 2024 Jun 20;17(6):812. doi: 10.3390/ph17060812.
Efforts have been made to improve the therapeutic efficiency of tumor treatments, and metal-organic frameworks (MOFs) have shown excellent potential in tumor therapy. Monotherapy for the treatment of tumors has limited effects due to the limitation of response conditions and inevitable multidrug resistance, which seriously affect the clinical therapeutic effect. In this study, we chose to construct a multiple cascade synergistic tumor drug delivery system MIL-101(Fe)-DOX-TCPP-MnO@PDA-Ag (MDTM@P-Ag) using MOFs as drug carriers. Under near-infrared (NIR) laser irradiation, 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin (TCPP) and Ag NPs loaded on MDTM@P-Ag can be activated to generate cytotoxic reactive oxygen species (ROS) and achieve photothermal conversion, thus effectively inducing the apoptosis of tumor cells and achieving a combined photodynamic/photothermal therapy. Once released at the tumor site, manganese dioxide (MnO) can catalyze the decomposition of hydrogen peroxide (HO) in the acidic microenvironment of the tumor to generate oxygen (O) and alleviate the hypoxic environment of the tumor. Fe/Mn will mediate a Fenton/Fenton-like reaction to generate cytotoxic hydroxyl radicals (·OH), while depleting the high concentration of glutathione (GSH) in the tumor, thus enhancing the chemodynamic therapeutic effect. The successful preparation of the tumor drug delivery system and its good synergistic chemodynamic/photodynamic/photothermal therapeutic effect in tumor treatment can be demonstrated by the experimental results of material characterization, performance testing and in vitro experiments.
人们一直在努力提高肿瘤治疗的疗效,金属有机框架材料(MOFs)在肿瘤治疗中显示出了巨大的潜力。由于反应条件的限制和不可避免的多药耐药性,肿瘤的单一疗法效果有限,严重影响了临床治疗效果。在本研究中,我们选择以MOFs为药物载体构建一种多重级联协同肿瘤药物递送系统MIL-101(Fe)-DOX-TCPP-MnO@PDA-Ag(MDTM@P-Ag)。在近红外(NIR)激光照射下,负载在MDTM@P-Ag上的5,10,15,20-四(4-羧基苯基)卟啉(TCPP)和银纳米颗粒(Ag NPs)可被激活产生活性细胞毒性氧物种(ROS)并实现光热转换,从而有效诱导肿瘤细胞凋亡并实现光动力/光热联合治疗。一旦在肿瘤部位释放,二氧化锰(MnO)可在肿瘤的酸性微环境中催化过氧化氢(H₂O₂)分解产生氧气(O₂),缓解肿瘤的缺氧环境。铁/锰将介导芬顿/类芬顿反应产生活性细胞毒性羟基自由基(·OH),同时消耗肿瘤中高浓度的谷胱甘肽(GSH),从而增强化学动力学治疗效果。材料表征、性能测试和体外实验的结果证明了肿瘤药物递送系统的成功制备及其在肿瘤治疗中良好的化学动力学/光动力/光热协同治疗效果。