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基于 MOF(铁)的复合材料作为一种用于化学-光动力肿瘤治疗的独特纳米平台。

MOF(Fe)-derived composites as a unique nanoplatform for chemo-photodynamic tumor therapy.

机构信息

Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science and Engineering, Hubei University, Wuhan, Hubei, 430062, China.

Division of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430022, P. R. China.

出版信息

J Mater Chem B. 2022 Nov 3;10(42):8760-8770. doi: 10.1039/d2tb01691e.

Abstract

Fe-based metal-organic frameworks (MOFs) can be used for chemodynamic therapy (CDT) for tumors due to their unique Fenton-like effects and porous and biodegradable nature. The adsorption and transport of small molecule drugs by their structure has attracted much attention. Herein, MnO@NH-MIL101(Fe)@Ce6-F127 nanoparticles (MNMCF NPs) were synthesized using a facile solvothermal strategy. The small molecule photosensitizer Ce6 was adsorbed by MOFs to improve the biocompatibility of Ce6 and give it high bioavailability when injected intravenously. When the MNMCF NPs reached the tumor site, Fe-based MOFs exhibited Fenton-like properties, producing ˙OH and showing CDT effects. MnO could specifically respond to produce O in a tumor microenvironment, thereby improving the tumor hypoxia state and enhancing the efficacy of photodynamic therapy (PDT) by Ce6. Both the and experiments showed that the MNMCF-guided CDT/PDT combination therapy could effectively ablate tumors without the drawbacks of poor tolerability and potential long-term side effects. Therefore, the prepared MNMCF NPs can be used as promising candidates for synergistic CDT/PDT tumor therapy.

摘要

基于铁的金属-有机骨架(MOFs)由于其独特的类 Fenton 效应、多孔和可生物降解的特性,可用于肿瘤的化学动力学治疗(CDT)。其结构对小分子药物的吸附和传输引起了广泛关注。在此,采用简便的溶剂热策略合成了 MnO@NH-MIL101(Fe)@Ce6-F127 纳米粒子(MNMCF NPs)。小分子光敏剂 Ce6 通过 MOFs 吸附,提高了 Ce6 的生物相容性,使其在静脉注射时具有较高的生物利用度。当 MNMCF NPs 到达肿瘤部位时,基于铁的 MOFs 表现出类 Fenton 特性,产生˙OH 并表现出 CDT 效应。MnO 可以特异性地响应,在肿瘤微环境中产生 O2,从而改善肿瘤缺氧状态,增强 Ce6 的光动力治疗(PDT)效果。和实验均表明,MNMCF 引导的 CDT/PDT 联合治疗能够有效地消融肿瘤,而没有耐受性差和潜在长期副作用的缺点。因此,所制备的 MNMCF NPs 可作为协同 CDT/PDT 肿瘤治疗的有前途的候选物。

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