Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), NMPA Key Laboratory for Research and Evaluation of Radiopharmaceuticals (National Medical Products Administration), Department of Nuclear Medicine, Peking University Cancer Hospital and Institute, Beijing, 100142, China.
Molecular Imaging Program at Stanford (MIPS) and Bio-X Program, Department of Radiology, School of Medicine, Stanford University, Stanford, CA, 94305, USA.
Small. 2021 May;17(21):e2100378. doi: 10.1002/smll.202100378. Epub 2021 Apr 18.
An integrated molecular probe for combined tumor-targeted multimodal imaging and therapy in the era of precision medicine requires a multiplexed platform that simultaneously has high targeting specificity, versatile conjugation capability, and biocompatibility. Here, a novel biocompatible melanin nanoprobe (PMNs-II-813) coupled with a highly specific prostate-specific membrane antigen small molecule inhibitor is developed for the targeted multimodal diagnosis and treatment of prostate cancer. The melanin nanoparticles demonstrate photoacoustic imaging and photothermal therapy (PTT) functionalities via strong near-infrared absorption. The imaging contrast agents Zr and Mn are stably conjugated to the nanoparticles for positron emission tomography (PET) and magnetic resonance imaging (MRI). Fusion PET/MRI with PMNs-II-813 enables the monitoring of treatment effects in real time and lasts for more than 1 week, demonstrating the capability for multimodal theranostics in prostate cancer. Labeling with a therapeutic radionuclide, I, simultaneously endows the nanoprobe with the capability for radioisotope therapy (RIT) and PTT under triple-modal imaging guidance. Combined PTT and RIT has an inhibitory effect on prostate cancer growth (tumor inhibition rate of ≈93% 20 days after treatment), which is significantly better than that with the single treatment. Overall, it is believed that PMNs-II-813 has potential for clinical translation to treat prostate cancer.
在精准医疗时代,用于联合肿瘤靶向多模式成像和治疗的综合分子探针需要一个同时具有高靶向特异性、多功能偶联能力和生物相容性的多路复用平台。在这里,开发了一种新型的生物相容性黑色素纳米探针 (PMNs-II-813),它与一种高度特异的前列腺特异性膜抗原小分子抑制剂偶联,用于前列腺癌的靶向多模式诊断和治疗。黑色素纳米颗粒通过强近红外吸收显示出光声成像和光热治疗 (PTT) 功能。成像造影剂 Zr 和 Mn 被稳定地结合到纳米颗粒上,用于正电子发射断层扫描 (PET) 和磁共振成像 (MRI)。PMNs-II-813 的融合 PET/MRI 能够实时监测治疗效果,持续时间超过 1 周,显示出在前列腺癌中进行多模式治疗的能力。放射性核素 I 的标记同时赋予纳米探针进行放射性同位素治疗 (RIT) 和在三重模式成像引导下的 PTT 的能力。联合 PTT 和 RIT 对前列腺癌生长具有抑制作用(治疗后 20 天肿瘤抑制率约为 93%),明显优于单一治疗。总体而言,相信 PMNs-II-813 具有治疗前列腺癌的临床转化潜力。