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Calcium-Based Nanoparticles Accelerate Skin Wound Healing

INTRODUCTION: Nanoparticles (NPs) are small entities that consist of a hydroxyapatite core, which can bind ions, proteins, and other organic molecules from the surrounding environment. These small conglomerations can influence environmental calcium levels and have the potential to modulate calcium h...

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Detalles Bibliográficos
Autores principales: Kawai, Kenichiro, Larson, Barrett J., Ishise, Hisako, Carre, Antoine Lyonel, Nishimoto, Soh, Longaker, Michael, Lorenz, H. Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206933/
https://www.ncbi.nlm.nih.gov/pubmed/22073267
http://dx.doi.org/10.1371/journal.pone.0027106
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author Kawai, Kenichiro
Larson, Barrett J.
Ishise, Hisako
Carre, Antoine Lyonel
Nishimoto, Soh
Longaker, Michael
Lorenz, H. Peter
author_facet Kawai, Kenichiro
Larson, Barrett J.
Ishise, Hisako
Carre, Antoine Lyonel
Nishimoto, Soh
Longaker, Michael
Lorenz, H. Peter
author_sort Kawai, Kenichiro
collection PubMed
description INTRODUCTION: Nanoparticles (NPs) are small entities that consist of a hydroxyapatite core, which can bind ions, proteins, and other organic molecules from the surrounding environment. These small conglomerations can influence environmental calcium levels and have the potential to modulate calcium homeostasis in vivo. Nanoparticles have been associated with various calcium-mediated disease processes, such as atherosclerosis and kidney stone formation. We hypothesized that nanoparticles could have an effect on other calcium-regulated processes, such as wound healing. In the present study, we synthesized pH-sensitive calcium-based nanoparticles and investigated their ability to enhance cutaneous wound repair. METHODS: Different populations of nanoparticles were synthesized on collagen-coated plates under various growth conditions. Bilateral dorsal cutaneous wounds were made on 8-week-old female Balb/c mice. Nanoparticles were then either administered intravenously or applied topically to the wound bed. The rate of wound closure was quantified. Intravenously injected nanoparticles were tracked using a FLAG detection system. The effect of nanoparticles on fibroblast contraction and proliferation was assessed. RESULTS: A population of pH-sensitive calcium-based nanoparticles was identified. When intravenously administered, these nanoparticles acutely increased the rate of wound healing. Intravenously administered nanoparticles were localized to the wound site, as evidenced by FLAG staining. Nanoparticles increased fibroblast calcium uptake in vitro and caused contracture of a fibroblast populated collagen lattice in a dose-dependent manner. Nanoparticles also increased the rate of fibroblast proliferation. CONCLUSION: Intravenously administered, calcium-based nanoparticles can acutely decrease open wound size via contracture. We hypothesize that their contraction effect is mediated by the release of ionized calcium into the wound bed, which occurs when the pH-sensitive nanoparticles disintegrate in the acidic wound microenvironment. This is the first study to demonstrate that calcium-based nanoparticles can have a therapeutic benefit, which has important implications for the treatment of wounds.
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spelling pubmed-32069332011-11-09 Calcium-Based Nanoparticles Accelerate Skin Wound Healing Kawai, Kenichiro Larson, Barrett J. Ishise, Hisako Carre, Antoine Lyonel Nishimoto, Soh Longaker, Michael Lorenz, H. Peter PLoS One Research Article INTRODUCTION: Nanoparticles (NPs) are small entities that consist of a hydroxyapatite core, which can bind ions, proteins, and other organic molecules from the surrounding environment. These small conglomerations can influence environmental calcium levels and have the potential to modulate calcium homeostasis in vivo. Nanoparticles have been associated with various calcium-mediated disease processes, such as atherosclerosis and kidney stone formation. We hypothesized that nanoparticles could have an effect on other calcium-regulated processes, such as wound healing. In the present study, we synthesized pH-sensitive calcium-based nanoparticles and investigated their ability to enhance cutaneous wound repair. METHODS: Different populations of nanoparticles were synthesized on collagen-coated plates under various growth conditions. Bilateral dorsal cutaneous wounds were made on 8-week-old female Balb/c mice. Nanoparticles were then either administered intravenously or applied topically to the wound bed. The rate of wound closure was quantified. Intravenously injected nanoparticles were tracked using a FLAG detection system. The effect of nanoparticles on fibroblast contraction and proliferation was assessed. RESULTS: A population of pH-sensitive calcium-based nanoparticles was identified. When intravenously administered, these nanoparticles acutely increased the rate of wound healing. Intravenously administered nanoparticles were localized to the wound site, as evidenced by FLAG staining. Nanoparticles increased fibroblast calcium uptake in vitro and caused contracture of a fibroblast populated collagen lattice in a dose-dependent manner. Nanoparticles also increased the rate of fibroblast proliferation. CONCLUSION: Intravenously administered, calcium-based nanoparticles can acutely decrease open wound size via contracture. We hypothesize that their contraction effect is mediated by the release of ionized calcium into the wound bed, which occurs when the pH-sensitive nanoparticles disintegrate in the acidic wound microenvironment. This is the first study to demonstrate that calcium-based nanoparticles can have a therapeutic benefit, which has important implications for the treatment of wounds. Public Library of Science 2011-11-02 /pmc/articles/PMC3206933/ /pubmed/22073267 http://dx.doi.org/10.1371/journal.pone.0027106 Text en Kawai, et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kawai, Kenichiro
Larson, Barrett J.
Ishise, Hisako
Carre, Antoine Lyonel
Nishimoto, Soh
Longaker, Michael
Lorenz, H. Peter
Calcium-Based Nanoparticles Accelerate Skin Wound Healing
title Calcium-Based Nanoparticles Accelerate Skin Wound Healing
title_full Calcium-Based Nanoparticles Accelerate Skin Wound Healing
title_fullStr Calcium-Based Nanoparticles Accelerate Skin Wound Healing
title_full_unstemmed Calcium-Based Nanoparticles Accelerate Skin Wound Healing
title_short Calcium-Based Nanoparticles Accelerate Skin Wound Healing
title_sort calcium-based nanoparticles accelerate skin wound healing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206933/
https://www.ncbi.nlm.nih.gov/pubmed/22073267
http://dx.doi.org/10.1371/journal.pone.0027106
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