• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一锅法合成 pH 敏感型 MOF 并集成葡萄糖氧化酶用于肿瘤的光动力/光热联合治疗。

One-Pot Synthesis of a pH-Sensitive MOF Integrated with Glucose Oxidase for Amplified Tumor Photodynamic/Photothermal Therapy.

机构信息

Department of Molecular Imaging, School of Medical Technology, Qiqihar Medical University, Qiqihar, Heilongjiang 161006, P.R. China.

Department of Gastroenterology of Southwest Hospital Army Medical University (Third Military Medical University), Chongqing 400038, P.R. China.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 18;16(37):49083-49091. doi: 10.1021/acsami.4c10006. Epub 2024 Sep 4.

DOI:10.1021/acsami.4c10006
PMID:39228328
Abstract

Photothermal therapy (PTT) and photodynamic therapy (PDT) provide targeted approaches to cancer treatment, but each therapy has inherent limitations such as insufficient tissue penetration, uneven heat distribution, extreme hypoxia, and overexpressed HSP90 in tumor cells. To address these issues, herein, by encapsulating the IR780 dye and glucose oxidase (GOx) enzyme within ZIF-8 nanoparticles, we created a versatile system capable of combining photodynamic and enhanced photothermal therapy. The integration of the IR780 dye facilitated the generation of reactive oxygen species and hyperthermia upon light activation, enabling dual-mode cancer cell ablation. Moreover, GOx catalyzes the decomposition of glucose into gluconic acid and hydrogen peroxide, leading to the inhibition of ATP production and downregulation of heat shock protein 90 (HSP90) expression, sensitizing cancer cells to heat-induced cytotoxicity. This synergistic combination resulted in significantly improved therapeutic outcomes. Both in vitro and in vivo results validated that the nanoplatform demonstrated superior specificity and favorable therapeutic responses. Our innovative approach represents a promising strategy for overcoming current limitations in cancer treatments and offers the potential for clinical translation in the future.

摘要

光热疗法(PTT)和光动力疗法(PDT)为癌症治疗提供了靶向方法,但每种疗法都有其内在的局限性,例如组织穿透不足、热量分布不均匀、极度缺氧以及肿瘤细胞中 HSP90 过表达。为了解决这些问题,本文通过将 IR780 染料和葡萄糖氧化酶(GOx)酶封装在 ZIF-8 纳米粒子内,创建了一种多功能系统,能够结合光动力和增强光热疗法。IR780 染料的整合促进了光激活时活性氧和高热的产生,实现了双模癌细胞消融。此外,GOx 催化葡萄糖分解为葡萄糖酸和过氧化氢,导致 ATP 产生抑制和热休克蛋白 90(HSP90)表达下调,使癌细胞对热诱导的细胞毒性敏感。这种协同组合导致治疗效果显著提高。体外和体内结果均验证了该纳米平台具有优异的特异性和良好的治疗反应。我们的创新方法代表了克服癌症治疗当前局限性的有前途的策略,并为未来的临床转化提供了潜力。

相似文献

1
One-Pot Synthesis of a pH-Sensitive MOF Integrated with Glucose Oxidase for Amplified Tumor Photodynamic/Photothermal Therapy.一锅法合成 pH 敏感型 MOF 并集成葡萄糖氧化酶用于肿瘤的光动力/光热联合治疗。
ACS Appl Mater Interfaces. 2024 Sep 18;16(37):49083-49091. doi: 10.1021/acsami.4c10006. Epub 2024 Sep 4.
2
In Vitro Synergistic Photodynamic, Photothermal, Chemodynamic, and Starvation Therapy Performance of Chlorin e6 Immobilized, Polydopamine-Coated Hollow, Porous Ceria-Based, Hypoxia-Tolerant Nanozymes Carrying a Cascade System.载级联体系的氯 e6 固载、聚多巴胺包覆的中空多孔氧化铈缺氧耐受纳米酶的体外协同光动力、光热、化学动力学和饥饿治疗性能
ACS Appl Bio Mater. 2024 May 20;7(5):2781-2793. doi: 10.1021/acsabm.3c01181. Epub 2024 Feb 21.
3
Ultrasmall iridium-encapsulated porphyrin metal-organic frameworks for enhanced photodynamic/catalytic therapy by producing reactive oxygen species storm.超小尺寸的铱包裹卟啉金属有机框架通过产生活性氧物种风暴来增强光动力/催化治疗。
J Colloid Interface Sci. 2025 Jan;677(Pt B):1022-1033. doi: 10.1016/j.jcis.2024.08.144. Epub 2024 Aug 22.
4
Synthesis of Au@MOF core-shell hybrids for enhanced photodynamic/photothermal therapy.金@MOF 核壳杂化物的合成用于增强光动力/光热治疗。
J Mater Chem B. 2021 Sep 7;9(33):6646-6657. doi: 10.1039/d1tb00800e. Epub 2021 Aug 9.
5
Zeolitic Imidazolate Framework Platform for Combinational Starvation Therapy and Oxygen Self-Sufficient Photodynamic Therapy against a Hypoxia Tumor.沸石咪唑酯骨架平台用于联合饥饿疗法和氧气自足的光动力疗法治疗缺氧肿瘤。
ACS Appl Bio Mater. 2021 May 17;4(5):4413-4421. doi: 10.1021/acsabm.1c00174. Epub 2021 Apr 15.
6
Oxygen Self-Sufficient Core-Shell Metal-Organic Framework-Based Smart Nanoplatform for Enhanced Synergistic Chemotherapy and Photodynamic Therapy.基于自给氧核壳型金属有机骨架的智能纳米平台用于增强协同化学治疗和光动力治疗。
ACS Appl Mater Interfaces. 2020 Jun 3;12(22):24662-24674. doi: 10.1021/acsami.0c08534. Epub 2020 May 22.
7
X-ray triggered scintillator versatile nanocatalytic platform for synergistic photodynamic/chemodynamic therapy.X 射线触发闪烁多功能纳米催化平台用于协同光动力/化学动力治疗。
Talanta. 2025 Jan 1;281:126886. doi: 10.1016/j.talanta.2024.126886. Epub 2024 Sep 14.
8
Synthesis of dual-stimuli responsive metal organic framework-coated iridium oxide nanocomposite functionalized with tumor targeting albumin-folate for synergistic photodynamic/photothermal cancer therapy.合成具有肿瘤靶向白蛋白-叶酸功能化的双重刺激响应型金属有机框架包覆氧化铱纳米复合材料,用于协同光动力/光热癌症治疗。
Drug Deliv. 2022 Dec;29(1):3142-3154. doi: 10.1080/10717544.2022.2127973.
9
Hyaluronic acid-based multifunctional nanoplatform for glucose deprivation-enhanced chemodynamic/photothermal synergistic cancer therapy.基于透明质酸的多功能纳米平台用于葡萄糖剥夺增强的化学动力学/光热协同癌症治疗。
Int J Biol Macromol. 2024 Aug;275(Pt 1):133428. doi: 10.1016/j.ijbiomac.2024.133428. Epub 2024 Jun 25.
10
Defect-engineered porphyrinic metal-organic framework nanoparticles for targeted multimodal cancer phototheranostics.用于靶向多模态癌症光热诊疗的缺陷工程化卟啉金属有机框架纳米颗粒
Chem Commun (Camb). 2021 Apr 22;57(33):4035-4038. doi: 10.1039/d0cc07903k.

引用本文的文献

1
Donor modulation brings all-in-one phototheranostics for NIR-II imaging-guided type-I photodynamic/photothermal synergistic cancer therapy.供体调控实现了用于近红外二区成像引导的I型光动力/光热协同癌症治疗的一体化光诊疗。
Chem Sci. 2025 Feb 4;16(12):5089-5098. doi: 10.1039/d4sc08685f. eCollection 2025 Mar 19.
2
Climate friendly MOFs synthesis for drug delivery systems by integrating AI, intelligent manufacturing, and quantum solutions in industry 6.0 sustainable approach.通过在工业6.0可持续发展方法中整合人工智能、智能制造和量子解决方案,实现用于药物递送系统的气候友好型金属有机框架合成。
Toxicol Res (Camb). 2025 Jan 22;14(1):tfaf011. doi: 10.1093/toxres/tfaf011. eCollection 2025 Feb.