An intelligent hypoxia-relieving chitosan-based nanoplatform for enhanced targeted chemo-sonodynamic combination therapy on lung cancer

被引:30
作者
Zhang, Peixia [1 ]
Zhang, Lu [1 ]
Wang, Jun [1 ]
Zhu, Lisheng [1 ]
Li, Ziying [1 ]
Chen, Haijun [2 ]
Gao, Yu [1 ]
机构
[1] Fuzhou Univ, Coll Chem, Canc Metastasis Alert & Prevent Ctr, Fujian Prov Key Lab Canc Metastasis Chemoprevent, Fuzhou 350108, Fujian, Peoples R China
[2] Fuzhou Univ, Fujian Prov Key Lab Canc Metastasis Chemoprevent, Fuzhou 350108, Fujian, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Non-small cell lung cancer; Chitosan; Sonodynamic therapy; Erlotinib; Perfluoroctylbromide; Hypoxia; PHOTODYNAMIC THERAPY; DRUG-DELIVERY; CO-DELIVERY; RESISTANCE; METASTASIS; ANTICANCER; ERLOTINIB; OXYGEN;
D O I
10.1016/j.carbpol.2021.118655
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The clinical efficacy of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs)-based targeted molecular therapies (TMT) is inevitably hampered by the development of acquired drug resistance in non-small cell lung cancer (NSCLC) treatment. Sonodymanic therapy (SDT) is a promising new cancer treatment approach, but its effects are restricted by tumor hypoxia. Herein, a nanoplatform fabricated by erlotinib-modified chitosan loading sonosensitizer hematoporphyrin (HP) and oxygen-storing agent perfluorooctyl bromide (PFOB), namely CEPH, was developed to deliver HP to erlotinib-sensitive cells. CEPH with ultrasound could alleviate hypoxia inside the three-dimensional multicellular tumor spheroids, suppress NSCLC cell growth under normoxic or hypoxic condition, and enhance TMT/SDT synergistic effects through elevated production of reactive oxygen species, decrease of mitochondrial membrane potential, and down-regulation of the expression of the proteins EGFR, p-EGFR, and HIF-1 alpha. Hence, CEPH could be a potential nanoplatform to improve the efficacy of oxygen dependent SDT and overcome hypoxia-induced TMT resistance for enhanced synergistic TMT/SDT.
引用
收藏
页数:13
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