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肿瘤微环境响应型可生物降解纳米医学用于自增强协同化疗、光热和化学动力学治疗。

Tumor Microenvironment-Responsive Biodegradable Nanomedicine for Self-Enhanced Synergistic Chemo-, Photothermal, and Chemodynamic Therapy.

机构信息

Academy of Chinese Medical Sciences, Henan University of Chinese Medicine, Zhengzhou 450046, China.

College of Pharmacy, Henan University of Chinese Medicine, Zhengzhou 450046, China.

出版信息

ACS Appl Mater Interfaces. 2024 Oct 2;16(39):52023-52035. doi: 10.1021/acsami.4c09671. Epub 2024 Sep 20.

Abstract

The nanoscale multidrug codelivery system for synergistic therapy is an effective strategy for tumor treatment. However, the low drug delivery efficiency and poor therapeutic effects limit its application. Here, based on the coordination effect of Artemisinin (Art), quercetin (Qc), and Fe, we had constructed a safe and efficient carrier-free hyaluronic acid (HA)-modified Art-Fe-Qc nanoparticles (AFQ@HA NPs) for enhanced chemotherapy/photothermal therapy (PTT)-chemodynamic therapy (CDT) synergistic therapy, which achieved an ultrahigh drug loading efficiency and a multifunction anticancer strategy. The results showed that high drug loading was achieved based on drug coordination self-assembly, with Art and Qc contents of 38.6 and 42.7%, respectively. At the same time, based on the Qc-Fe coordination molecular network, the system had excellent photothermal conversion performance with an efficiency of 57.3% and could effectively inhibit the expression of HSP70, achieving enhanced PTT. Further, under the stimulation of excessive HO and glutathione (GSH) in the tumor microenvironment, the AFQ@HA NPs were continuously degraded, while releasing Art and Fe/Fe to achieve iron ion-enhanced CDT. The results of in vitro and in vivo experiments showed that AFQ@HA NPs could achieve chemotherapy-PTT-CDT synergistic therapy in response to tumor microenvironment by passively targeting and actively targeting tumor cells with CD44, demonstrating its excellent targeted antitumor effects.

摘要

用于协同治疗的纳米级多药共递系统是肿瘤治疗的有效策略。然而,低药物递送效率和差的治疗效果限制了其应用。在这里,基于青蒿素(Art)、槲皮素(Qc)和 Fe 的协同作用,我们构建了一种安全有效的无载体透明质酸(HA)修饰的青蒿素-Fe-Qc 纳米粒子(AFQ@HA NPs),用于增强化学疗法/光热治疗(PTT)-化学动力学治疗(CDT)协同治疗,实现了超高的药物负载效率和多功能抗癌策略。结果表明,基于药物配位自组装实现了高药物负载,Art 和 Qc 的含量分别为 38.6%和 42.7%。同时,基于 Qc-Fe 配位分子网络,该系统具有出色的光热转换性能,效率为 57.3%,可有效抑制 HSP70 的表达,实现增强的 PTT。此外,在肿瘤微环境中过量 HO 和谷胱甘肽(GSH)的刺激下,AFQ@HA NPs 不断降解,同时释放 Art 和 Fe/Fe 以实现铁离子增强的 CDT。体外和体内实验结果表明,AFQ@HA NPs 能够通过与 CD44 被动靶向和主动靶向肿瘤细胞,响应肿瘤微环境实现化疗-PTT-CDT 协同治疗,表现出优异的靶向抗肿瘤效果。

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