4.8 Article

Anchoring Group-Mediated Radiolabeling of Inorganic Nanoparticles-A Universal Method for Constructing Nuclear Medicine Imaging Nanoprobes

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 7, 页码 8838-8846

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c23907

关键词

radiolabeling; nanoprobes; nuclear medicine; multimodality imaging; nanomedicine

资金

  1. National Key Research and Development Program of China [2018YFA0208800]
  2. National Natural Science Foundation of China [82130059, 82172003, 81720108024]
  3. Nature Science Foundation of Jiangsu Higher Education Institutions of China [20KJA150006]
  4. Natural Science Foundation of Jiangsu Province [BK20191418]
  5. Suzhou Key Industry Technology Innovation Projects [SYG202036]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

向作者/读者索取更多资源

This study demonstrates the universality of a simple and efficient radiolabeling method, LAGMERAL, for constructing radioactive nanoprobes. The method utilizes a diphosphonate-polyethylene glycol (DP-PEG) group on the surface of inorganic nanoparticles for efficient radiolabeling. The resulting nanoprobes exhibit high radiolabeling stability and biocompatibility, making them promising for sensitive tumor diagnosis. This research highlights the importance and potential of LAGMERAL in nuclear medicine imaging.
Nuclear medicine imaging has aroused great interest in the design and synthesis of versatile radioactive nanoprobes, while most of the methods developed for radiolabeling nanoprobes are difficult to satisfy the criteria of clinical translation, including easy operation, mild labeling conditions, high efficiency, and high radiolabeling stability. Herein, we demonstrated the universality of a simple but efficient radiolabeling method recently developed for constructing nuclear imaging nanoprobes, that is, ligand anchoring group-mediated radiolabeling (LAGMERAL). In this method, a diphosphonate-polyethylene glycol (DP-PEG) decorating on the surface of inorganic nanoparticles plays an essential role. In principle, owing to the strong binding affinity to a great variety of metal ions, it can not only endow the underlying nanoparticles containing metal ions including some main group metal ions, transition metal ions, and lanthanide metal ions with excellent colloidal stability and biocompatibility but also enable efficient radiolabeling through the diphosphonate group. Based on this assumption, inorganic nanoparticles such as Fe3O4 nanoparticles, NaGdF4:Yb,Tm nanoparticles, and Cu2-xS nanoparticles, as representatives of functional inorganic nanoparticles suitable for different imaging modalities including magnetic resonance imaging (MRI), upconversion luminescence imaging (UCL), and photoacoustic imaging (PAI), respectively, were chosen to be radiolabeled with different kinds of radionuclides such as SPECT nuclides (e.g., (99)mTc), PET nuclides (e.g., Ga-68), and therapeutic SPECT nuclides (e.g., Lu-177) to demonstrate the reliability of the LAGMERAL approach. The experimental results showed that the obtained nanoprobes exhibited high radiolabeling stability, and the whole radiolabeling process had negligible impacts on the physical and chemical properties of the initial nanoparticles. Through passive targeting SPECT/MRI of glioma tumor, active targeting SPECT/UCL of colorectal cancer, and SPECT/PAI of lymphatic metastasis, the outstanding potentials of the resulting radioactive nanoprobes for sensitive tumor diagnosis were demonstrated, manifesting the feasibility and efficiency of LAGMERAL.

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