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Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI
We synthesized manganese ferrite (MnFe(2)O(4)) nanoparticles of different sizes by varying pH during chemical co-precipitation procedure and modified their surfaces with polysaccharide chitosan (CS) to investigate characteristics of hyperthermia and magnetic resonance imaging (MRI). Structural featu...
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/PMC7699708/ https://www.ncbi.nlm.nih.gov/pubmed/33233590 http://dx.doi.org/10.3390/nano10112297 |
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author | Islam, Khairul Haque, Manjurul Kumar, Arup Hoq, Amitra Hyder, Fahmeed Hoque, Sheikh Manjura |
author_facet | Islam, Khairul Haque, Manjurul Kumar, Arup Hoq, Amitra Hyder, Fahmeed Hoque, Sheikh Manjura |
author_sort | Islam, Khairul |
collection | PubMed |
description | We synthesized manganese ferrite (MnFe(2)O(4)) nanoparticles of different sizes by varying pH during chemical co-precipitation procedure and modified their surfaces with polysaccharide chitosan (CS) to investigate characteristics of hyperthermia and magnetic resonance imaging (MRI). Structural features were analyzed by X-ray diffraction (XRD), high-resolution transmission electron microscopy (TEM), selected area diffraction (SAED) patterns, and Mössbauer spectroscopy to confirm the formation of superparamagnetic MnFe(2)O(4) nanoparticles with a size range of 5–15 nm for pH of 9–12. The hydrodynamic sizes of nanoparticles were less than 250 nm with a polydispersity index of 0.3, whereas the zeta potentials were higher than 30 mV to ensure electrostatic repulsion for stable colloidal suspension. MRI properties at 7T demonstrated that transverse relaxation (T(2)) doubled as the size of CS-coated MnFe(2)O(4) nanoparticles tripled in vitro. However, longitudinal relaxation (T(1)) was strongest for the smallest CS-coated MnFe(2)O(4) nanoparticles, as revealed by in vivo positive contrast MRI angiography. Cytotoxicity assay on HeLa cells showed CS-coated MnFe(2)O(4) nanoparticles is viable regardless of ambient pH, whereas hyperthermia studies revealed that both the maximum temperature and specific loss power obtained by alternating magnetic field exposure depended on nanoparticle size and concentration. Overall, these results reveal the exciting potential of CS-coated MnFe(2)O(4) nanoparticles in MRI and hyperthermia studies for biomedical research. |
format | Online Article Text |
id | pubmed-7699708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76997082020-11-29 Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI Islam, Khairul Haque, Manjurul Kumar, Arup Hoq, Amitra Hyder, Fahmeed Hoque, Sheikh Manjura Nanomaterials (Basel) Article We synthesized manganese ferrite (MnFe(2)O(4)) nanoparticles of different sizes by varying pH during chemical co-precipitation procedure and modified their surfaces with polysaccharide chitosan (CS) to investigate characteristics of hyperthermia and magnetic resonance imaging (MRI). Structural features were analyzed by X-ray diffraction (XRD), high-resolution transmission electron microscopy (TEM), selected area diffraction (SAED) patterns, and Mössbauer spectroscopy to confirm the formation of superparamagnetic MnFe(2)O(4) nanoparticles with a size range of 5–15 nm for pH of 9–12. The hydrodynamic sizes of nanoparticles were less than 250 nm with a polydispersity index of 0.3, whereas the zeta potentials were higher than 30 mV to ensure electrostatic repulsion for stable colloidal suspension. MRI properties at 7T demonstrated that transverse relaxation (T(2)) doubled as the size of CS-coated MnFe(2)O(4) nanoparticles tripled in vitro. However, longitudinal relaxation (T(1)) was strongest for the smallest CS-coated MnFe(2)O(4) nanoparticles, as revealed by in vivo positive contrast MRI angiography. Cytotoxicity assay on HeLa cells showed CS-coated MnFe(2)O(4) nanoparticles is viable regardless of ambient pH, whereas hyperthermia studies revealed that both the maximum temperature and specific loss power obtained by alternating magnetic field exposure depended on nanoparticle size and concentration. Overall, these results reveal the exciting potential of CS-coated MnFe(2)O(4) nanoparticles in MRI and hyperthermia studies for biomedical research. MDPI 2020-11-20 /pmc/articles/PMC7699708/ /pubmed/33233590 http://dx.doi.org/10.3390/nano10112297 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 Islam, Khairul Haque, Manjurul Kumar, Arup Hoq, Amitra Hyder, Fahmeed Hoque, Sheikh Manjura Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI |
title | Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI |
title_full | Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI |
title_fullStr | Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI |
title_full_unstemmed | Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI |
title_short | Manganese Ferrite Nanoparticles (MnFe(2)O(4)): Size Dependence for Hyperthermia and Negative/Positive Contrast Enhancement in MRI |
title_sort | manganese ferrite nanoparticles (mnfe(2)o(4)): size dependence for hyperthermia and negative/positive contrast enhancement in mri |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699708/ https://www.ncbi.nlm.nih.gov/pubmed/33233590 http://dx.doi.org/10.3390/nano10112297 |
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