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In vivo Preclinical Tumor-Specific Imaging of Superparamagnetic Iron Oxide Nanoparticles Using Magnetic Particle Imaging for Cancer Diagnosis.
Park, Sang-Jin; Han, Seung Ro; Kang, Yun Hee; Lee, Eun-Jin; Kim, Eu-Gene; Hong, Hyobong; Jeong, Jae-Chan; Lee, Myung-Shin; Lee, Seung-Hoon; Song, Dae-Yong.
Afiliação
  • Park SJ; Department of Anatomy and Neuroscience, Eulji University School of Medicine, Daejeon, Korea.
  • Han SR; Eulji Biomedical Science Research Institute, Eulji University School of Medicine, Daejeon, Korea.
  • Kang YH; Department of Microbiology and Immunology, Eulji University School of Medicine, Daejeon, Korea.
  • Lee EJ; Eulji Biomedical Science Research Institute, Eulji University School of Medicine, Daejeon, Korea.
  • Kim EG; Department of Microbiology and Immunology, Eulji University School of Medicine, Daejeon, Korea.
  • Hong H; Department of Anatomy and Neuroscience, Eulji University School of Medicine, Daejeon, Korea.
  • Jeong JC; Department of Anatomy and Neuroscience, Eulji University School of Medicine, Daejeon, Korea.
  • Lee MS; Artifcial Intelligence Research Laboratory, Electronics and Telecommunications Research Institute (ETRI), Daejeon, Korea.
  • Lee SH; Artifcial Intelligence Research Laboratory, Electronics and Telecommunications Research Institute (ETRI), Daejeon, Korea.
  • Song DY; Eulji Biomedical Science Research Institute, Eulji University School of Medicine, Daejeon, Korea.
Int J Nanomedicine ; 17: 3711-3722, 2022.
Article em En | MEDLINE | ID: mdl-36051351
ABSTRACT

Purpose:

Magnetic particle imaging (MPI) is an emerging radiation-free, non-invasive three-dimensional tomographic technology that can visualize the concentrations of superparamagnetic iron oxide nanoparticles (SPIONs). To verify the applicability of the previously proposed point-of-care testing MPI (PoCT-MPI) in medical diagnosis and therapeutics, we imaged SPIONs in animal tumor models.

Methods:

CT26 or MC38 mouse colon carcinoma cells (2 × 106 cells) were subcutaneously injected into the right flank of BALB/c mice. SPIONs were either injected directly into the tumor lesions in the intratumoral group or through tail veins in the intravenous group. CT26 and MC38 tumor models were examined both intratumorally and intravenously to confirm the biological availability of SPIONs using PoCT-MPI.

Results:

Signals were observed in the tumor lesions from day 1 to day 7. This is the first study to successfully image the pathological region and show the biodistribution of SPIONs in CT26 tumor models using the recently developed PoCT-MPI technology. Furthermore, MC38 tumor models were examined, resulting in similar images to those of the CT26 tumor model in both intratumoral and intravenous groups.

Conclusion:

The present study demonstrates the biological applicability of PoCT-MPI, which promises to be a powerful diagnostic and therapeutic technique in biomedical imaging.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas de Magnetita / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: Int J Nanomedicine Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas de Magnetita / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: Int J Nanomedicine Ano de publicação: 2022 Tipo de documento: Article