Biodegradable mesoporous nanocomposites with dual-targeting function for enhanced anti-tumor therapy

被引:35
作者
Gao, Shan [1 ,2 ]
Liu, Yuli [3 ]
Liu, Meng [2 ]
Yang, Dongjuan [3 ]
Zhang, Mingming [3 ]
Shi, Kai [1 ]
机构
[1] Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin 300350, Peoples R China
[2] Shandong Univ, Sch Pharmaceut Sci, Dept Pharmaceut, Jinan 250012, Shandong, Peoples R China
[3] Shenyang Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, Shenyang 117004, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Tumor-associated macrophages; Biodegradable; Ordered mesoporous nanocomposites; Indocyanine green; Photothermal therapy; Photodynamic therapy; TUMOR-ASSOCIATED MACROPHAGES; INDOCYANINE GREEN; SILICA NANOPARTICLES; GOLD NANOCLUSTERS; DELIVERY; NANOSPHERES; ACID; DRUG; NANOPROBES; ACTIVATION;
D O I
10.1016/j.jconrel.2021.11.044
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tumor-associated macrophages (TAMs), the main components of infiltrating leukocytes in tumors, often play a key role in promoting cancer development and progression. The tumor-specific microenvironment forces the phenotype of tumor-infiltrating to evolve in a direction favorable to tumor development, that is, the generation of M2-like TAMs. Consequently, the dual intervention of cancer cells and tumor microenvironment has become a research hotspot in the field of tumor immunotherapy. In this contribution, we developed pH-sensitive meso-porous calcium silicate nanocomposites (MCNs) encapsulated with indocyanine green (ICG) to enable the effective combination of photothermal therapy (PTT) and photodynamic therapy (PDT) triggered by the 808 nm near-infrared (NIR) light. The mannose and hyaluronic acid-grafted MCNs specifically targeted TAMs and tumor cells and promoted cell apoptosis both in vitro and in vivo. This paper revealed that irradiation of ICG loaded MCNs with NIR can produce a potent hyperthermia and induce abundant intracellular singlet oxygen generation in the target cells. These results suggest that the novel nanoplatform is believed to facilitate the delivery of chemotherapeutic agents to the tumor microenvironment (TME) to enhance the effects of tumor treatment.
引用
收藏
页码:383 / 398
页数:16
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