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A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells
Despite developments in pulmonary radiotherapy, radiation-induced lung toxicity remains a problem. More sensitive lung imaging able to increase the accuracy of diagnosis and radiotherapy may help reduce this problem. Super-paramagnetic iron oxide nanoparticles are used in imaging, but without furthe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084491/ https://www.ncbi.nlm.nih.gov/pubmed/32120819 http://dx.doi.org/10.3390/ijms21051613 |
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author | Chakraborty, Amlan Royce, Simon G. Selomulya, Cordelia Plebanski, Magdalena |
author_facet | Chakraborty, Amlan Royce, Simon G. Selomulya, Cordelia Plebanski, Magdalena |
author_sort | Chakraborty, Amlan |
collection | PubMed |
description | Despite developments in pulmonary radiotherapy, radiation-induced lung toxicity remains a problem. More sensitive lung imaging able to increase the accuracy of diagnosis and radiotherapy may help reduce this problem. Super-paramagnetic iron oxide nanoparticles are used in imaging, but without further modification can cause unwanted toxicity and inflammation. Complex carbohydrate and polymer-based coatings have been used, but simpler compounds may provide additional benefits. Herein, we designed and generated super-paramagnetic iron oxide nanoparticles coated with the neutral natural dietary amino acid glycine (GSPIONs), to support non-invasive lung imaging and determined particle biodistribution, as well as understanding the impact of the interaction of these nanoparticles with lung immune cells. These GSPIONs were characterized to be crystalline, colloidally stable, with a size of 12 ± 5 nm and a hydrodynamic diameter of 84.19 ± 18 nm. Carbon, Hydrogen, Nitrogen (CHN) elemental analysis estimated approximately 20.2 × 10(3) glycine molecules present per nanoparticle. We demonstrated that it is possible to determine the biodistribution of the GSPIONs in the lung using three-dimensional (3D) ultra-short echo time magnetic resonance imaging. The GSPIONs were found to be taken up selectively by alveolar macrophages and neutrophils in the lung. In addition, the GSPIONs did not cause changes to airway resistance or induce inflammatory cytokines. Alveolar macrophages and neutrophils are critical regulators of pulmonary inflammatory diseases, including allergies, infections, asthma and chronic obstructive pulmonary disease (COPD). Therefore, pulmonary Magnetic Resonance (MR) imaging and preferential targeting of these lung resident cells by our nanoparticles offer precise imaging tools, which can be utilized to develop precision targeted radiotherapy as well as diagnostic tools for lung cancer, thereby having the potential to reduce the pulmonary complications of radiation. |
format | Online Article Text |
id | pubmed-7084491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70844912020-03-24 A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells Chakraborty, Amlan Royce, Simon G. Selomulya, Cordelia Plebanski, Magdalena Int J Mol Sci Article Despite developments in pulmonary radiotherapy, radiation-induced lung toxicity remains a problem. More sensitive lung imaging able to increase the accuracy of diagnosis and radiotherapy may help reduce this problem. Super-paramagnetic iron oxide nanoparticles are used in imaging, but without further modification can cause unwanted toxicity and inflammation. Complex carbohydrate and polymer-based coatings have been used, but simpler compounds may provide additional benefits. Herein, we designed and generated super-paramagnetic iron oxide nanoparticles coated with the neutral natural dietary amino acid glycine (GSPIONs), to support non-invasive lung imaging and determined particle biodistribution, as well as understanding the impact of the interaction of these nanoparticles with lung immune cells. These GSPIONs were characterized to be crystalline, colloidally stable, with a size of 12 ± 5 nm and a hydrodynamic diameter of 84.19 ± 18 nm. Carbon, Hydrogen, Nitrogen (CHN) elemental analysis estimated approximately 20.2 × 10(3) glycine molecules present per nanoparticle. We demonstrated that it is possible to determine the biodistribution of the GSPIONs in the lung using three-dimensional (3D) ultra-short echo time magnetic resonance imaging. The GSPIONs were found to be taken up selectively by alveolar macrophages and neutrophils in the lung. In addition, the GSPIONs did not cause changes to airway resistance or induce inflammatory cytokines. Alveolar macrophages and neutrophils are critical regulators of pulmonary inflammatory diseases, including allergies, infections, asthma and chronic obstructive pulmonary disease (COPD). Therefore, pulmonary Magnetic Resonance (MR) imaging and preferential targeting of these lung resident cells by our nanoparticles offer precise imaging tools, which can be utilized to develop precision targeted radiotherapy as well as diagnostic tools for lung cancer, thereby having the potential to reduce the pulmonary complications of radiation. MDPI 2020-02-27 /pmc/articles/PMC7084491/ /pubmed/32120819 http://dx.doi.org/10.3390/ijms21051613 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chakraborty, Amlan Royce, Simon G. Selomulya, Cordelia Plebanski, Magdalena A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells |
title | A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells |
title_full | A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells |
title_fullStr | A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells |
title_full_unstemmed | A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells |
title_short | A Novel Approach for Non-Invasive Lung Imaging and Targeting Lung Immune Cells |
title_sort | novel approach for non-invasive lung imaging and targeting lung immune cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084491/ https://www.ncbi.nlm.nih.gov/pubmed/32120819 http://dx.doi.org/10.3390/ijms21051613 |
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