生物安全
磁共振成像
黑磷
表面改性
纳米技术
化学
材料科学
核磁共振
生物医学工程
医学
病理
放射科
光电子学
物理化学
物理
作者
Xiao Huang,Yuanyuan Zhao,Miao Zhou,Yun Guo,Haiyun Wang,Yuanyuan Chen,Jian Peng
标识
DOI:10.1002/advs.202503654
摘要
Abstract Despite the critical role of contrast‐enhanced magnetic resonance imaging (MRI) in clinical diagnostics, current contrast agents face dual challenges: metallic formulations provoke biosafety concerns while organic radicals exhibit transient imaging windows. To overcome these limitations, a radical‐engineered 2D black phosphorus (2D BP) nanoplatform is reported through atomic‐scale conjugation of aminoferrocene, creating a stable complex with enhanced electron spin resonance, named FcP. The covalent coupling strategy establishes persistent T 2 ‐weighted contrast capability. Subsequent hyaluronic acid (HA) functionalization endows the HA‐FcP system with CD44‐specific targeting, achieving 1.7‐fold higher plaque accumulation than non‐targeted counterparts in apolipoprotein E‐deficient models. Remarkably, this nanostructure enables continuous MRI visualization of atherosclerotic lesions for 120 h post‐injection. Systematic biosafety evaluation demonstrates >90% cell viability and normal hematological parameters. This work pioneers a new paradigm for MRI contrast agents through spin state manipulation of 2D materials, providing a translational platform for precision cardiovascular diagnostics.
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