Jiang Xu, Pan Jiachen, Gong Zhichao, Meng Shuxian
School of Chemical Engineering and Technology, Tianjin University, Tianjin 300354, P. R. China.
ACS Appl Mater Interfaces. 2025 Jul 23;17(29):41816-41824. doi: 10.1021/acsami.5c10247. Epub 2025 Jul 13.
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 (NaYF:20%Yb,2%Er@NaYF:20%Yb@NaNdF) 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 (Nd → Yb → Er), 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.
传统金属有机框架材料(MOFs)的短吸收波长由于组织穿透性差,严重限制了其在光动力疗法(PDT)中的应用。将MOFs与上转换纳米颗粒(UCNPs)结合以发挥它们的互补优势,已成为一种变革性策略。在此,设计了一种近红外(NIR)响应的核壳异质结构(UGD),它将镧系元素掺杂的UCNPs(NaYF:20%Yb,2%Er@NaYF:20%Yb@NaNdF)与基于硼二吡咯亚甲基(BODIPY)的钆金属有机框架(GD)整合在一起。UCNP核通过级联能量转移(Nd→Yb→Er)将808 nm近红外光转换为绿色发射光(515 - 564 nm),精确激活GD光敏剂,从而在深部组织中有效产生活性氧(ROS)。体外研究表明,在505和808 nm照射下细胞毒性相当,而体内实验表明,808 nm光具有更强的肿瘤抑制效果(体积缩小90%,而505 nm光为65%)。系统的生物分布分析证实了肿瘤靶向积累和快速代谢清除。UGD平台将近红外穿透深度与MOF增强的光敏剂稳定性相结合,为精确光动力诊疗提供了一种变革性策略。