National Engineering Research Centre for Biomaterials, Sichuan University, Chengdu 610064, P. R. China.
J Mater Chem B. 2021 Feb 25;9(7):1846-1857. doi: 10.1039/d0tb02725a.
Based on widely used photoacoustic imaging (PAI) and photothermal properties of polydopamine (PDA), a multifunctional Gd-PDA-Ce6@Gd-MOF (GPCG) nanosystem with a core-shell structure and strong imaging ability was constructed. Benefitting from the metal-organic framework (MOF) structure, GPCG nanoparticles (NPs) showed enhanced magnetic resonance imaging (MRI) ability with high relaxation rates (r1 = 13.72 mM-1 s-1 and r2 = 216.14 mM-1 s-1). The MRI effect of Gd ions combined with the PAI effect of PDA, giving GPCG NPs a dual-modal imaging ability. The core, mainly composed of PDA and photodynamic photosensitizer chlorin e6 (Ce6), achieved photothermal/photodynamic therapy (PTT/PDT) synergistic performance. Besides, to overcome the unexpected release of Ce6, the MOF shell realized pH-sensitive release and a high local concentration. Through in vivo studies, we concluded that GPCG NPs show a good inhibitory effect on tumor growth. In conclusion, we successfully obtained a GPCG theranostic nanoplatform and paved the way for subsequent design of imaging guided therapeutic nanostructures based on metal-doped PDA.
基于聚多巴胺(PDA)广泛应用的光声成像(PAI)和光热特性,构建了具有核壳结构和强成像能力的多功能 Gd-PDA-Ce6@Gd-MOF(GPCG)纳米系统。受益于金属-有机骨架(MOF)结构,GPCG 纳米颗粒(NPs)表现出增强的磁共振成像(MRI)能力,具有高弛豫率(r1 = 13.72 mM-1 s-1 和 r2 = 216.14 mM-1 s-1)。Gd 离子的 MRI 效应与 PDA 的 PAI 效应相结合,赋予 GPCG NPs 双模式成像能力。核心主要由 PDA 和光动力光敏剂氯代卟啉 e6(Ce6)组成,实现了光热/光动力治疗(PTT/PDT)协同性能。此外,为了克服 Ce6 的意外释放,MOF 壳实现了 pH 敏感释放和局部高浓度。通过体内研究,我们得出结论,GPCG NPs 对肿瘤生长具有良好的抑制作用。总之,我们成功获得了 GPCG 治疗性纳米平台,并为随后设计基于金属掺杂 PDA 的成像引导治疗性纳米结构铺平了道路。