脂质体
阿霉素
肽
靶向治疗
胶质瘤
医学
药理学
癌症研究
化学
化疗
材料科学
纳米技术
癌症
内科学
生物化学
作者
Hongyan Li,Rong Gan,Jiadi Liu,Duling Xu,Qiyue Zhang,Haidong Tian,Huijun Guo,Haijun Wang,Zhimin Wang,Xianwu Zeng
标识
DOI:10.1016/j.mtbio.2025.101455
摘要
Ga-labeled peptide-Lipo@Dox. Lipo@Dox with peptide modification demonstrated stable Dox loading, small sizes (<40 nm), and enrichment in the tumor region of the mouse brain. Peptide-Lipo@Dox treatment inhibited the Tie-2/Akt/Foxo-1 pathway, thereby inhibiting cell invasion and migration, cell viability, and colony-forming ability of U87-MG cells. Lipo@Dox peptide modification showed a better suppression of glioma development than Lipo@Dox. Thus, the ANGPT2-specific peptides were successfully designed, and the PEGylated liposome modified with ANGPT2-specific peptide served as part of a potent delivery method for integrative glioma-targeted imaging and therapy.
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