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Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors
BACKGROUND: Late diagnosis of lung cancer is one of the leading causes of higher mortality in lung cancer patients worldwide. Significant research attention has focused on the use of magnetic resonance imaging (MRI) based nano contrast agents to efficiently locate cancer tumors for surgical removal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952886/ https://www.ncbi.nlm.nih.gov/pubmed/35337331 http://dx.doi.org/10.1186/s12951-022-01355-3 |
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author | Thangudu, Suresh Yu, Chun-Chieh Lee, Chin-Lai Liao, Min-Chiao Su, Chia-Hao |
author_facet | Thangudu, Suresh Yu, Chun-Chieh Lee, Chin-Lai Liao, Min-Chiao Su, Chia-Hao |
author_sort | Thangudu, Suresh |
collection | PubMed |
description | BACKGROUND: Late diagnosis of lung cancer is one of the leading causes of higher mortality in lung cancer patients worldwide. Significant research attention has focused on the use of magnetic resonance imaging (MRI) based nano contrast agents to efficiently locate cancer tumors for surgical removal or disease diagnostics. Although contrast agents offer significant advantages, further clinical applications require improvements in biocompatibility, biosafety and efficacy. RESULTS: To address these challenges, we fabricated ultra-fine Iron Carbonate Nanoparticles (FeCO(3) NPs) for the first time via modified literature method. Synthesized NPs exhibit ultra-fine size (~ 17 nm), good dispersibility and excellent stability in both aqueous and biological media. We evaluated the MR contrast abilities of FeCO(3) NPs and observed remarkable T2 weighted MRI contrast in a concentration dependent manner, with a transverse relaxivity (r2) value of 730.9 ± 4.8 mM(−1) S(−1)at 9.4 T. Moreover, the r2 values of present FeCO(3) NPs are respectively 1.95 and 2.3 times higher than the clinically approved contrast agents Resovist(®) and Friedx at same 9.4 T MR scanner. FeCO(3) NPs demonstrate an enhanced T2 weighted contrast for in vivo lung tumors within 5 h of post intravenous administration with no apparent systemic toxicity or induction of inflammation observed in in vivo mice models. CONCLUSION: The excellent biocompatibility and T2 weighted contrast abilities of FeCO(3) NPs suggest potential for future clinical use in early diagnosis of lung tumors. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01355-3. |
format | Online Article Text |
id | pubmed-8952886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89528862022-03-26 Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors Thangudu, Suresh Yu, Chun-Chieh Lee, Chin-Lai Liao, Min-Chiao Su, Chia-Hao J Nanobiotechnology Research BACKGROUND: Late diagnosis of lung cancer is one of the leading causes of higher mortality in lung cancer patients worldwide. Significant research attention has focused on the use of magnetic resonance imaging (MRI) based nano contrast agents to efficiently locate cancer tumors for surgical removal or disease diagnostics. Although contrast agents offer significant advantages, further clinical applications require improvements in biocompatibility, biosafety and efficacy. RESULTS: To address these challenges, we fabricated ultra-fine Iron Carbonate Nanoparticles (FeCO(3) NPs) for the first time via modified literature method. Synthesized NPs exhibit ultra-fine size (~ 17 nm), good dispersibility and excellent stability in both aqueous and biological media. We evaluated the MR contrast abilities of FeCO(3) NPs and observed remarkable T2 weighted MRI contrast in a concentration dependent manner, with a transverse relaxivity (r2) value of 730.9 ± 4.8 mM(−1) S(−1)at 9.4 T. Moreover, the r2 values of present FeCO(3) NPs are respectively 1.95 and 2.3 times higher than the clinically approved contrast agents Resovist(®) and Friedx at same 9.4 T MR scanner. FeCO(3) NPs demonstrate an enhanced T2 weighted contrast for in vivo lung tumors within 5 h of post intravenous administration with no apparent systemic toxicity or induction of inflammation observed in in vivo mice models. CONCLUSION: The excellent biocompatibility and T2 weighted contrast abilities of FeCO(3) NPs suggest potential for future clinical use in early diagnosis of lung tumors. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01355-3. BioMed Central 2022-03-25 /pmc/articles/PMC8952886/ /pubmed/35337331 http://dx.doi.org/10.1186/s12951-022-01355-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Thangudu, Suresh Yu, Chun-Chieh Lee, Chin-Lai Liao, Min-Chiao Su, Chia-Hao Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors |
title | Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors |
title_full | Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors |
title_fullStr | Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors |
title_full_unstemmed | Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors |
title_short | Magnetic, biocompatible FeCO(3) nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors |
title_sort | magnetic, biocompatible feco(3) nanoparticles for t2-weighted magnetic resonance imaging of in vivo lung tumors |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952886/ https://www.ncbi.nlm.nih.gov/pubmed/35337331 http://dx.doi.org/10.1186/s12951-022-01355-3 |
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