Thymoquinone Glucuronide Conjugated Magnetic Nanoparticle for Bimodal Imaging and Treatment of Cancer as a Novel Theranostic Platform

Author:

İnce İskender1ORCID,Müftüler Zümrüt Biber1,Medine E.İlker1,Güldü Özge Kozguş1,Takan Gökhan1,Ergönül Ayşegül2,Parlak Yasemin3,Yıldırım Yeliz4,Çakar Burcu5,Bilgin Elvan Sayit3,Aras Ömer6,Göker Erdem5,Ünak Perihan1ORCID

Affiliation:

1. Ege University, Department of Nuclear Application, Institute of Nuclear Sciences, Izmir, Turkey

2. Ege University, Faculty of Medicine Department of Chest Surgery, Izmir, Turkey

3. Celal Bayar University, Faculty of Medicine Department of Nuclear Medicine, Manisa, Turkey

4. Ege University, Center for Drug R&D and Pharmacokinetic Applications (ARGEFAR), Izmir, Turkey

5. Ege University Faculty of Medicine, Division of Medical Oncology, Izmir, Turkey

6. Memorial Sloan Kettering Cancer Center, Department of Radiology, New York, United States

Abstract

Background: Theranostic oncology combines therapy and diagnosis and is a new field of medicine that specifically targets the disease by using targeted molecules to destroy the cancerous cells without damaging the surrounding healthy tissues. Objective: We aimed to develop a tool that exploits enzymatic TQ release from glucuronide (G) for the imaging and treatment of lung cancer. We added magnetic nanoparticles (MNP) to enable magnetic hyperthermia and MRI, as well as 131I to enable SPECT imaging and radionuclide therapy. Methods: A glucuronide derivative of thymoquinone (TQG) was enzymatically synthesized and conjugated with the synthesized MNP and then radioiodinated with 131I. New Zealand white rabbits were used in SPECT and MRI studies, while tumor modeling studies were performed on 6–7- week-old nude mice utilized with bioluminescence imaging. Results: Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) spectra confirmed the expected structures of TQG. The dimensions of nanoparticles were below 10 nm and they had rather polyhedral shapes. Nanoparticles were radioiodinated with 131I with over 95% yield. In imaging studies, in xenograft models, tumor volume was significantly reduced in TQGMNP-treated mice but not in non-treated mice. Among mice treated intravenously with TQGMNP, xenograft tumor models disappeared after 10 and 15 days, respectively. Conclusion: Our findings suggest that TQGMNP in solid, semi-solid and liquid formulations can be developed using different radiolabeling nuclides for applications in multimodality imaging (SPECT and MRI). By altering the characteristics of radionuclides, TQGMNP may ultimately be used not only for diagnosis but also for the treatment of various cancers as an in vitro diagnostic kit for the diagnosis of beta glucuronidase-rich cancers.

Funder

NIH/ NCI Cancer Center

Turkish Scientific Research Council- Health Sciences Research Support Group

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmacology,Radiology Nuclear Medicine and imaging

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. An Overview of In Vivo Imaging Techniques;Recent Progress in Pharmaceutical Nanobiotechnology: A Medical Perspective;2023-12-27

2. Methods for Radiolabeling Nanoparticles (Part 3): Therapeutic Use;Biomolecules;2023-08-12

3. Radionuclide-based theranostics — a promising strategy for lung cancer;European Journal of Nuclear Medicine and Molecular Imaging;2023-03-16

4. Transforming Nuclear Medicine with Nanoradiopharmaceuticals;ACS Nano;2022-03-16

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