纳米载体
光热治疗
药物输送
细胞毒性
癌细胞
生物相容性
靶向给药
药品
药理学
抗药性
化学
毒品携带者
纳米技术
胶体金
癌症研究
癌症
医学
材料科学
体外
纳米颗粒
生物
生物化学
内科学
微生物学
有机化学
作者
Maliheh Entezari,Ghazaleh Gholamiyan Yousef Abad,Behnaz Sedghi,Reyhaneh Ettehadi,Shafagh Asadi,Razieh Beiranvand,Negar Haratian,Seyedeh Sara Karimian,Ali Jebali,Ramin Khorrami,Mohammad Arad Zandieh,Hamidreza Saebfar,Kiavash Hushmandi,Shokooh Salimimoghadam,Mohsen Rashidi,Afshin Taheriazam,Mehrdad Hashemi,Yavuz Nuri Ertaş
标识
DOI:10.1016/j.envres.2023.115673
摘要
The application of nanoarchitectures in cancer therapy seems to be beneficial for the delivery of antitumor drugs. In recent years, attempts have been made to reverse drug resistance, one of the factors threatening the lives of cancer patients worldwide. Gold nanoparticles (GNPs) are metal nanostructures with a variety of advantageous properties, such as tunable size and shape, continuous release of chemicals, and simple surface modification. This review focuses on the application of GNPs for the delivery of chemotherapy agents in cancer therapy. Utilizing GNPs results in targeted delivery and increased intracellular accumulation. Besides, GNPs can provide a platform for the co-delivery of anticancer agents and genetic tools with chemotherapeutic compounds to exert a synergistic impact. Furthermore, GNPs can promote oxidative damage and apoptosis by triggering chemosensitivity. Due to their capacity for providing photothermal therapy, GNPs can enhance the cytotoxicity of chemotherapeutic agents against tumor cells. The pH-, redox-, and light-responsive GNPs are beneficial for drug release at the tumor site. For the selective targeting of cancer cells, surface modification of GNPs with ligands has been performed. In addition to improving cytotoxicity, GNPs can prevent the development of drug resistance in tumor cells by facilitating prolonged release and loading low concentrations of chemotherapeutics while maintaining their high antitumor activity. As described in this study, the clinical use of chemotherapeutic drug-loaded GNPs is contingent on enhancing their biocompatibility.
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