β-Cyclodextrin-cholic acid-hyaluronic acid polymer coated Fe3O4-graphene oxide nanohybrids as local chemo-photothermal synergistic agents for enhanced liver tumor therapy

光热治疗 胆酸 透明质酸 纳米载体 体内 胆汁酸 肝癌 化学 纳米技术 癌细胞 月桂酸 材料科学 癌症 癌症研究 生物物理学 药物输送 肝细胞癌 生物化学 医学 脂肪酸 内科学 生物技术 解剖 生物
作者
Chaochao Wen,Rina Cheng,Tao Gong,Yu Huang,Dan Li,Xu‐Hua Zhao,Baofeng Yu,Dan Su,Zhiling Song,Wenting Liang
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier]
卷期号:199: 111510-111510 被引量:42
标识
DOI:10.1016/j.colsurfb.2020.111510
摘要

Synergistic photochemical therapy with high performance and weak side effects is of great importance in hepatocellular carcinoma (HCC) treatment, therefore ingenious construct of nano-based therapy agents with accurate drug delivery and high photothermal conversion efficiency is of critical to the cancer therapy. Herein, an organic-inorganic hybrid nanomaterial ([email protected]) has been constructed successfully by coating the β-cyclodextrin-cholic acid-hyaluronic acid polymer (CD-CA-HA) onto the Fe3O4-graphene oxide (MGO). The [email protected] revealed satisfactory multiple-targeted features including the cholic acid supplied hepatic-target, CD44-receptor target of hyaluronic acid and magnetic target of Fe3O4. Meanwhile, the hydrophobic antitumor drug camptothecin (CPT) was easily loaded by [email protected] to form the [email protected]/CPT nanocomposite, and the maximum theoretical adsorption capacity can reach 847.4 mg/g. Based on the facile photothermal response of MGO, the near-infrared radiation (808 nm) induced local hyperthermia was directly generated the apoptosis of tumor cells while triggered the release of CPT. Comparing with other kinds of cancer cells and normal hepatocyte cells, this PCT system provides a significant inhibitory effect for the liver cancer cells in vitro. Furthermore, the synergistic photochemical therapy presented the strong antitumor effect (the tumor inhibition rate > 90 %) in vivo. Thus, this study provided a promising multiple-targeted nanocarrier for chemo-photothermal combination therapy of liver cancer.

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