Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, School of Biomedical Engineering, Health Science Center, Shenzhen University, Shenzhen, 518060, China.
Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, 518060, China.
Adv Mater. 2017 Sep;29(35). doi: 10.1002/adma.201701013. Epub 2017 Jul 13.
Integration of magnetic resonance imaging (MRI) and other imaging modalities is promising to furnish complementary information for accurate cancer diagnosis and imaging-guided therapy. However, most gadolinium (Gd)-chelator MR contrast agents are limited by their relatively low relaxivity and high risk of released-Gd-ions-associated toxicity. Herein, a radionuclide- Cu-labeled doxorubicin-loaded polydopamine (PDA)-gadolinium-metallofullerene core-satellite nanotheranostic agent (denoted as CDPGM) is developed for MR/photoacoustic (PA)/positron emission tomography (PET) multimodal imaging-guided combination cancer therapy. In this system, the near-infrared (NIR)-absorbing PDA acts as a platform for the assembly of different moieties; Gd N@C , a kind of gadolinium metallofullerene with three Gd ions in one carbon cage, acts as a satellite anchoring on the surface of PDA. The as-prepared CDPGM NPs show good biocompatibility, strong NIR absorption, high relaxivity (r = 14.06 mM s ), low risk of release of Gd ions, and NIR-triggered drug release. In vivo MR/PA/PET multimodal imaging confirms effective tumor accumulation of the CDPGM NPs. Moreover, upon NIR laser irradiation, the tumor is completely eliminated with combined chemo-photothermal therapy. These results suggest that the CDPGM NPs hold great promise for cancer theranostics.
磁共振成像(MRI)与其他成像方式的融合有望为准确的癌症诊断和影像引导治疗提供补充信息。然而,大多数钆(Gd)螯合物磁共振对比剂的弛豫率相对较低,且存在释放的 Gd 离子相关毒性的风险较高。在此,我们开发了一种放射性核素- Cu 标记的阿霉素负载聚多巴胺(PDA)-钆-金属富勒烯核-卫星纳米诊疗剂(记为 CDPGM),用于磁共振/光声(PA)/正电子发射断层扫描(PET)多模态成像引导联合癌症治疗。在该系统中,近红外(NIR)吸收的 PDA 作为组装不同部分的平台;Gd N@C 是一种具有三个 Gd 离子在一个碳笼中的钆金属富勒烯,作为卫星锚定在 PDA 的表面。所制备的 CDPGM NPs 具有良好的生物相容性、强的 NIR 吸收、高弛豫率(r = 14.06 mM s)、低释放 Gd 离子的风险和 NIR 触发的药物释放。体内磁共振/光声/PET 多模态成像证实了 CDPGM NPs 对肿瘤的有效积累。此外,在近红外激光照射下,联合化疗-光热治疗可完全消除肿瘤。这些结果表明,CDPGM NPs 有望用于癌症治疗。