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DOI 10.1016/j.canlet.2018.03.002

Медицинская библиотека · Cancer letters · 2018

Enhanced anti-tumor efficacy of temozolomide-loaded carboxylated poly(amido-amine) combined with photothermal/photodynamic therapy for melanoma treatment.

Tang Jianqin, Zhou Huige, Hou Xiaoyang, Wang Liming, Li Yaxi, Pang Yanyu, Chen Chunying, Jiang Guan, Liu Yanqun

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Chemotherapy is an important treatment for malignant tumors; however, its efficacy and clinical application are limited by its side effects and drug resistance properties. Chemotherapy and phototherapy exhibit synergistic anti-tumor effects. In the present study, a carboxylated poly(amido-amine) (PAMAM) with low cytotoxicity was synthesized as a delivery nanocarrier for loading chemotherapeutic drugs, temozolomide (TMZ), and fluorescent dye indocyanine green (ICG). Hyaluronic acid (HA), which targets the CD44-overexpressing cancer cells, was modified on the nanocarrier surface to enhance the selective killing of melanoma cells. Temperature effect and singlet oxygen production experiments showed that the ICG-loaded nanoparticles exhibited good capability to generate heat and singlet oxygen under near-infrared (NIR) light (808 nm) irradiation. In vivo imaging measurement confirmed that the ICG-encapsulated nanoparticle was delivered successfully and effectively accumulated in the tumor site. In vitro and in vivo experiments revealed that the joint application of TMZ- and ICG-loaded nanoparticle can kill melanoma cells and suppress growth after NIR light irradiation. Thus, HA-modified carboxylated PAMAM loaded with TMZ and ICG serves as a promising nanoplatform for melanoma treatment.

Для цитирования: Tang Jianqin, Zhou Huige, Hou Xiaoyang, Wang Liming, Li Yaxi, Pang Yanyu, Chen Chunying, Jiang Guan, Liu Yanqun. Enhanced anti-tumor efficacy of temozolomide-loaded carboxylated poly(amido-amine) combined with photothermal/photodynamic therapy for melanoma treatment.. Cancer letters. 2018. DOI: 10.1016/j.canlet.2018.03.002.

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