材料科学
光子上转换
纳米颗粒
纳米技术
红外线的
光动力疗法
异质结
金属有机骨架
金属
光电子学
发光
光学
物理化学
有机化学
吸附
物理
化学
冶金
作者
Jiang Xu,Jiachen Pan,Zhichao Gong,Shuxian Meng
标识
DOI:10.1021/acsami.5c10247
摘要
The short absorption wavelengths of conventional metal-organic frameworks (MOFs) severely limits their photodynamic therapy (PDT) applications due to poor tissue penetration. Integrating MOFs with upconversion nanoparticles (UCNPs) to harness their complementary advantages has emerged as a transformative strategy. Here, a near-infrared (NIR)-responsive core@shell heterostructure (UGD) was engineered integrating lanthanide-doped UCNPs (NaYF4:20%Yb,2%Er@NaYF4:20%Yb@NaNdF4) with a boron-dipyrromethene (BODIPY)-based gadolinium metal-organic framework (GD). The UCNP core converts 808 nm NIR light into green emissions (515-564 nm) through cascade energy transfer (Nd3+ → Yb3+ → Er3+), precisely activating GD photosensitizers to enable effective ROS generation in deep tissues. In vitro studies revealed comparable cytotoxicity under 505 and 808 nm irradiation, while in vivo experiments demonstrated superior tumor suppression with 808 nm light (90% volume reduction vs 65% for 505 nm). Systematic biodistribution analysis confirmed tumor-targeted accumulation and rapid metabolic clearance. The UGD platform synergizes NIR penetration depth with MOF-enhanced photosensitizer stability, offering a transformative strategy for precision photodynamic theranostics.
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