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Doxorubicin-loaded micelles in tumor cell-specific chemotherapy

纳米载体 胶束 阿霉素 纳米医学 药物输送 癌细胞 光热治疗 细胞毒性 抗药性 药理学 癌症研究 癌症 化学 化疗 纳米技术 医学 材料科学 生物 生物化学 纳米颗粒 体外 内科学 水溶液 物理化学 微生物学
作者
Yasir Qasim Almajidi,Mustafa M. Kadhim,Fahad Alsaikhan,Abduladheem Turki Jalil,Nidhal Hassan Sayyid,Andrés Alexis Ramírez‐Coronel,Zanko Hassan Jawhar,Jitendra Gupta,Noushin Nabavi,Wei Yu,Yavuz Nuri Ertaş
出处
期刊:Environmental Research [Elsevier]
卷期号:227: 115722-115722 被引量:31
标识
DOI:10.1016/j.envres.2023.115722
摘要

Nanomedicine is a field that combines biology and engineering to improve disease treatment, particularly in cancer therapy. One of the promising techniques utilized in this area is the use of micelles, which are nanoscale delivery systems that are known for their simple preparation, high biocompatibility, small particle size, and the ability to be functionalized. A commonly employed chemotherapy drug, Doxorubicin (DOX), is an effective inhibitor of topoisomerase II that prevents DNA replication in cancer cells. However, its efficacy is frequently limited by resistance resulting from various factors, including increased activity of drug efflux transporters, heightened oncogenic factors, and lack of targeted delivery. This review aims to highlight the potential of micelles as new nanocarriers for delivering DOX and to examine the challenges involved with employing chemotherapy to treat cancer. Micelles that respond to changes in pH, redox, and light are known as stimuli-responsive micelles, which can improve the targeted delivery of DOX and its cytotoxicity by facilitating its uptake in tumor cells. Additionally, micelles can be utilized to administer a combination of DOX and other drugs and genes to overcome drug resistance mechanisms and improve tumor suppression. Furthermore, micelles can be used in phototherapy, both photodynamic and photothermal, to promote cell death and increase DOX sensitivity in human cancers. Finally, the alteration of micelle surfaces with ligands can further enhance their targeted delivery for cancer suppression.
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