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A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo

Stem cell imaging in vivo is critical to elucidate the homing, distribution, survival, and repair mechanisms and to evaluate the therapeutic effects of engrafted stem cells. Unfortunately, unimodal imaging of stem cells does not simultaneously satisfy all current requirements owing to their intrinsi...

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Autores principales: Zhang, Hua, Wang, Zhen-Jun, Wang, Ling-Jie, Li, Ting-Ting, He, Sheng, Li, Li-Ping, Li, Xiao-Yan, Liu, Shi-Jie, Li, Jian-Ding, Li, Si-Jin, Zhang, Rui-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074133/
https://www.ncbi.nlm.nih.gov/pubmed/35530687
http://dx.doi.org/10.1039/c9ra05937g
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author Zhang, Hua
Wang, Zhen-Jun
Wang, Ling-Jie
Li, Ting-Ting
He, Sheng
Li, Li-Ping
Li, Xiao-Yan
Liu, Shi-Jie
Li, Jian-Ding
Li, Si-Jin
Zhang, Rui-Ping
author_facet Zhang, Hua
Wang, Zhen-Jun
Wang, Ling-Jie
Li, Ting-Ting
He, Sheng
Li, Li-Ping
Li, Xiao-Yan
Liu, Shi-Jie
Li, Jian-Ding
Li, Si-Jin
Zhang, Rui-Ping
author_sort Zhang, Hua
collection PubMed
description Stem cell imaging in vivo is critical to elucidate the homing, distribution, survival, and repair mechanisms and to evaluate the therapeutic effects of engrafted stem cells. Unfortunately, unimodal imaging of stem cells does not simultaneously satisfy all current requirements owing to their intrinsic limitations. Obviously, bimodal or multimodal imaging of stem cells is a promising strategy for circumventing this issue. This study aimed to design and synthesize a novel dual-modal polyethylene glycol-modified magnetic nanoparticle (Fe(3+)-PEG-MNP) based on natural biomaterials including melanin and Fe ions for photoacoustic (PA) and magnetic resonance (MR) imaging of stem cells in vivo. The Fe(3+)-PEG-MNPs were characterized and their PA/MR imaging capability and cytotoxicity were evaluated. Bone marrow mesenchymal stem cells (BM-MSCs) labeled with Fe(3+)-PEG-MNPs were subjected to PA and MR imaging in vitro and in vivo. Consequently, Fe(3+)-PEG-MNPs displayed many superior properties, including ultra-small particle size, higher stability, water solubility, easy labeling of cells, lower cytotoxicity, high biosafety, excellent capability of PA/MR imaging, high sensitivity and long-term monitoring in vitro and in vivo. In particular, PA and MR signals of labeled BM-MSCs were maintained for at least 35 and 28 d, respectively, in vivo. Therefore, Fe(3+)-PEG-MNPs are ideal dual-modal PA/MR nanoparticles for non-invasive and effective monitoring of engrafted stem cells in vivo.
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spelling pubmed-90741332022-05-06 A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo Zhang, Hua Wang, Zhen-Jun Wang, Ling-Jie Li, Ting-Ting He, Sheng Li, Li-Ping Li, Xiao-Yan Liu, Shi-Jie Li, Jian-Ding Li, Si-Jin Zhang, Rui-Ping RSC Adv Chemistry Stem cell imaging in vivo is critical to elucidate the homing, distribution, survival, and repair mechanisms and to evaluate the therapeutic effects of engrafted stem cells. Unfortunately, unimodal imaging of stem cells does not simultaneously satisfy all current requirements owing to their intrinsic limitations. Obviously, bimodal or multimodal imaging of stem cells is a promising strategy for circumventing this issue. This study aimed to design and synthesize a novel dual-modal polyethylene glycol-modified magnetic nanoparticle (Fe(3+)-PEG-MNP) based on natural biomaterials including melanin and Fe ions for photoacoustic (PA) and magnetic resonance (MR) imaging of stem cells in vivo. The Fe(3+)-PEG-MNPs were characterized and their PA/MR imaging capability and cytotoxicity were evaluated. Bone marrow mesenchymal stem cells (BM-MSCs) labeled with Fe(3+)-PEG-MNPs were subjected to PA and MR imaging in vitro and in vivo. Consequently, Fe(3+)-PEG-MNPs displayed many superior properties, including ultra-small particle size, higher stability, water solubility, easy labeling of cells, lower cytotoxicity, high biosafety, excellent capability of PA/MR imaging, high sensitivity and long-term monitoring in vitro and in vivo. In particular, PA and MR signals of labeled BM-MSCs were maintained for at least 35 and 28 d, respectively, in vivo. Therefore, Fe(3+)-PEG-MNPs are ideal dual-modal PA/MR nanoparticles for non-invasive and effective monitoring of engrafted stem cells in vivo. The Royal Society of Chemistry 2019-10-31 /pmc/articles/PMC9074133/ /pubmed/35530687 http://dx.doi.org/10.1039/c9ra05937g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhang, Hua
Wang, Zhen-Jun
Wang, Ling-Jie
Li, Ting-Ting
He, Sheng
Li, Li-Ping
Li, Xiao-Yan
Liu, Shi-Jie
Li, Jian-Ding
Li, Si-Jin
Zhang, Rui-Ping
A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo
title A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo
title_full A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo
title_fullStr A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo
title_full_unstemmed A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo
title_short A dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo
title_sort dual-mode nanoparticle based on natural biomaterials for photoacoustic and magnetic resonance imaging of bone mesenchymal stem cells in vivo
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074133/
https://www.ncbi.nlm.nih.gov/pubmed/35530687
http://dx.doi.org/10.1039/c9ra05937g
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