血管生成拟态
化学
透明质酸
自愈水凝胶
生物相容性
细胞毒性
药物输送
内吞作用
胶束
移植
血管生成
癌症研究
药理学
生物物理学
细胞
细胞生物学
生物化学
转移
生物
医学
癌症
解剖
体外
高分子化学
内科学
水溶液
有机化学
物理化学
外科
作者
Rui Kang,Mengdi Song,Zhou Fang,Kehai Liu
标识
DOI:10.1080/1061186x.2022.2115047
摘要
Vasculogenic mimicry (VM) describes the phenomenon whereby fluid-conducting vessels are formed by highly invasive tumour cells, which supply blood to tumours during their early growth stages. Single antiangiogenic agents have limited inhibitory effects on VM, therefore, a multi-pathway anti-VM strategy is required. In this study, Apatinib (Apa) was coordinated with Cu2+ to form a Cu-Apa copper complex. The latter was loaded into oligo-hyaluronic acid (HA) polymeric micelles (HA-Chol) and subsequently embedded in Astragalus polysaccharide-based in situ hydrogels (APsGels) to generate Cu-Apa/HA-Chol@APsGels. In this system, Cu-Apa exerts the combined effects of Cu2+ and Apa to inhibit VM; HA-Chol micelles achieve targeted drug delivery and enhance endocytosis efficiency; APsGels realise sustained release of the drugs to ensure an anti-VM effect. This system demonstrated improved VM inhibition with low cytotoxicity and high biocompatibility, wound healing, and transwell invasion in three-dimensional cell cultured VM. Moreover, this system significantly inhibited VM formation and melanoma growth in a mouse tumour transplantation model. This study provides an effective strategy for inhibiting VM.
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