纳米医学
内化
光热治疗
氧化铁纳米粒子
癌细胞
纳米颗粒
化学
表皮生长因子受体
生物物理学
生物结合
配体(生物化学)
癌症研究
癌症
表皮生长因子
纳米技术
细胞
材料科学
受体
生物化学
医学
生物
内科学
作者
Barbara Freis,María de los Ángeles Ramírez,Sonia Furgiuele,Clémence Cheignon,Clémence Cheignon,Loı̈c J. Charbonnière,Céline Henoumont,Céline Kiefer,Damien Mertz,Christine Affolter-Zbaraszczuk,Florent Meyer,Mariana Tasso,Sylvie Bégin‐Colin,Mariana Tasso,Sylvie Bégin‐Colin
标识
DOI:10.1016/j.ijpharm.2023.122654
摘要
A major challenge in nanomedicine is designing nanoplatforms (NPFs) to selectively target abnormal cells to ensure early diagnosis and targeted therapy. Among developed NPFs, iron oxide nanoparticles (IONPs) are good MRI contrast agents and can be used for therapy by hyperthermia and as radio-sensitizing agents. Active targeting is a promising method for selective IONPs accumulation in cancer tissues and is generally performed by using targeting ligands (TL). Here, a TL specific for the epidermal growth factor receptor (EGFR) is bound to the surface of dendronized IONPs to produce nanostructures able to specifically recognize EGFR-positive FaDu and 93-Vu head and neck cancer cell lines. Several parameters were optimized to ensure a high coupling yield and to adequately quantify the amount of TL per nanoparticle. Nanostructures with variable amounts of TL on the surface were produced and evaluated for their potential to specifically target and be thereafter internalized by cells. Compared to the bare NPs, the presence of the TL at the surface was shown to be effective to enhance their internalization and to play a role in the total amount of iron present per cell.
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