Shikonin-Loaded Hollow Fe-MOF Nanoparticles for Enhanced Microwave Thermal Therapy

被引:8
|
作者
Chen, Lufeng [1 ]
Zhao, Dongming [1 ,2 ]
Ren, Xiangling [3 ,4 ]
Ren, Jun [3 ,4 ]
Meng, Xianwei [3 ,4 ]
Fu, Changhui [3 ,4 ]
Li, Xianfeng [1 ,2 ]
机构
[1] Shanxi Med Univ, Clin Med Sch & Hosp 1 1, Dept Radiat Oncol, Taiyuan 030001, Peoples R China
[2] Shanxi Med Univ, Basic Med Sch, Dept Pathol, Taiyuan 030001, Peoples R China
[3] Chinese Acad Sci, Tech Inst Phys & Chem, Lab Controllable Preparat & Applicat Nanomat, Beijing 100190, Peoples R China
[4] Chinese Acad Sci, Tech Inst Phys & Chem, CAS Key Lab Cryogen, Beijing 100190, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
shikonin; delivery nanosystem; microwave hyperthermia; microwave dynamic therapy; cancer therapy; metal-organic framework; PYRUVATE-KINASE M2; CANCER CELLS; TUMOR-THERAPY; HYPERTHERMIA; GLYCOLYSIS; CARCINOMA; NECROPTOSIS; GENERATION; INHIBITION; CAPACITY;
D O I
10.1021/acsbiomaterials.3c00644
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Microwave (MW) thermal therapy has been widely used for the treatment of cancer in clinics, but it still shows limited efficacy and a high recurrence rate owing to non-selective heat delivery and thermo-resistance. Regulating glycolysis shows great promise to improve MW thermal therapy since glycolysis plays an important role in thermoresistance, progression, metabolism, and recurrence. Herein, we developed a delivery nanosystem of shikonin (SK)- loaded and hyaluronic acid (HA)-modified hollow Fe-MOF (HFM), HFM@SK@ HA, as an efficient glycolysis-meditated agent to improve the efficacy of MW thermal therapy. The HFM@SK@HA nanosystem shows a high SK loading capacity of 31.7 wt %. The loaded SK can be effectively released from the HFM@SK@HA under the stimulation of an acidic tumor microenvironment and MW irradiation, overcoming the intrinsically low solubility and severe toxicity of SK. We also find that the HFM@SK@HA can not only greatly improve the heating effect of MW in the tumor site but also mediate MW-enhancing dynamic therapy efficiency by catalyzing the endogenous H2O2 to generate reactive oxygen species (ROS). As such, the MW irradiation treatment in the presence of HFM@SK@HA in vitro enables a highly improved anti-tumor efficacy due to the combined effect of released SK and generated ROS on inhibiting glycolysis in cancer cells. Our in vivo experiments show that the tumor inhibition rate is up to 94.75% +/- 3.63% with no obvious recurrence during the 2 weeks after treatment. This work provides a new strategy for improving the efficacy of MW thermal therapy.
引用
收藏
页码:5405 / 5417
页数:13
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