Multi-modal triggered-release sonodynamic/chemo/phototherapy synergistic nanocarriers for the treatment of colon cancer

被引:2
|
作者
Zhou, Yun [1 ]
Gao, Yueyang [1 ]
Yao, Nannan [1 ]
Lu, Guozhi [1 ]
Dong, Chuyu [2 ]
Wang, Kexin [2 ]
Zhang, Junfeng [3 ]
Sun, Jing [4 ]
Li, Ke [3 ]
Li, Xueping [1 ,3 ]
机构
[1] Xian Med Univ, Coll Clin Med, Xian, Peoples R China
[2] Xian Med Univ, Coll Clin Med 2, Xian, Peoples R China
[3] Xian Med Univ, Inst Basic & Translat Med, Translat & Res Ctr Prevent & Therapy Chron Dis, Xian Key Lab Prevent & Treatment Common Aging Dis, Xian, Peoples R China
[4] Xian Med Univ, Coll Med Technol, Xian, Peoples R China
来源
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY | 2024年 / 12卷
基金
芬兰科学院;
关键词
colon cancer; phototherapy; sonodynamic therapy; chemotherapy; muti-modal release; synergistic effect; PHOTOTHERMAL THERAPY; PHOTODYNAMIC THERAPY; SONODYNAMIC THERAPY; COLORECTAL-CANCER; ULTRASOUND; NANOPARTICLES; CAPSULES; APTAMER; OXIDE; DYE;
D O I
10.3389/fbioe.2024.1439883
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Most colon cancer patients are diagnosed at an advanced stage, with a grim prognosis. In clinical, various combination therapies have been employed to enhance the efficacy of colon cancer treatment. The essence of combined treatment is the judicious selection and combination of various treatment units. Phototherapy (PT), sonodynamic therapy (SDT), and chemotherapy are treatment modalities that rely on the active molecules to treat tumors, and have been demonstrated to synergistically enhance tumor treatment efficacy. However, the differences in the metabolism of active molecules and hypoxic microenvironment of tumors have limited the synergistic effects of the aforementioned methods. To address this significant issue, in this study, we utilized polydopamine (PDA) as the encapsulated material to form a rigid shell that contains the therapeutic molecules IR-780 and methotrexate (MTX) on the surface of perfluorohexane (PFH) microdroplets through self-assembling method to develop an SDT/chemotherapy/PT combined nanoparticles (SCP NPs). Transmission electron microscopy (TEM) revealed that the nanoparticles exhibited a hollow shell structure, with an average size of approximately 100 nm. SCP NPs have excellent stability and biocompatibility in both in vitro and in vivo. The absorption and emission spectrum of the loaded IR-780 did not exhibit any significant shift, and the photothermal temperature rose to 92 degrees C. Their ultrasonic cavitation effect was good and their cell inhibitory effect of MTX was maintained. SCP NPs can achieve multi-modal triggered release through ultrasound, laser irradiation, and pH, ensuring a simultaneous accumulation of therapeutic molecules in the tumor area and effectively alleviating tumor hypoxia. Additionally, both the near-infrared fluorescence (NIF) signal and the ultrasonic cavitation signal of the nanoparticles can be utilized for tracking and monitoring treatment efficacy. Most notably, SCP NPs exhibited outstanding synergistic treatment effects at low intervention levels, resulting in a 67% cure rate of tumors. These results provide an experimental basis for developing the new clinical treatments for colon cancer.
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页数:18
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