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In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery

Current treatments for osteoporosis and other bone degenerative diseases predominately rely on preventing further bone erosion rather than restoring bone mass, as the latter treatments can unintentionally trigger cancer development by undiscriminatingly promoting cell proliferation. One approach to...

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Autores principales: DuMez, Rachel, Miyanji, Esmail H., Corado-Santiago, Lesly, Barrameda, Bryle, Zhou, Yiqun, Hettiarachchi, Sajini D., Leblanc, Roger M., Skromne, Isaac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238062/
https://www.ncbi.nlm.nih.gov/pubmed/34176374
http://dx.doi.org/10.1080/10717544.2021.1938753
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author DuMez, Rachel
Miyanji, Esmail H.
Corado-Santiago, Lesly
Barrameda, Bryle
Zhou, Yiqun
Hettiarachchi, Sajini D.
Leblanc, Roger M.
Skromne, Isaac
author_facet DuMez, Rachel
Miyanji, Esmail H.
Corado-Santiago, Lesly
Barrameda, Bryle
Zhou, Yiqun
Hettiarachchi, Sajini D.
Leblanc, Roger M.
Skromne, Isaac
author_sort DuMez, Rachel
collection PubMed
description Current treatments for osteoporosis and other bone degenerative diseases predominately rely on preventing further bone erosion rather than restoring bone mass, as the latter treatments can unintentionally trigger cancer development by undiscriminatingly promoting cell proliferation. One approach to circumvent this problem is through the development of novel chemical carriers to deliver drug agents specifically to bones. We have recently shown that carbon nanodots (C-dots) synthesized from carbon nanopowder can bind with high affinity and specificity to developing bones in the larval zebrafish. Larval bones, however, are physiologically different from adult bones in their growth, repair, and regeneration properties. Here we report that C-dots can bind to adult zebrafish bones and that this binding is highly specific to areas of appositional growth. C-dots deposition occurred within 30 minutes after delivery and was highly selective, with bones undergoing regeneration and repair showing higher levels of C-dots deposition than bones undergoing normal homeostatic turnover. Importantly, C-dots deposition did not interfere with bone regeneration or the animal’s health. Together, our results establish C-dots as a potential novel vehicle for the targeted delivery of drugs to treat adult bone disease.
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spelling pubmed-82380622021-07-07 In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery DuMez, Rachel Miyanji, Esmail H. Corado-Santiago, Lesly Barrameda, Bryle Zhou, Yiqun Hettiarachchi, Sajini D. Leblanc, Roger M. Skromne, Isaac Drug Deliv Research Article Current treatments for osteoporosis and other bone degenerative diseases predominately rely on preventing further bone erosion rather than restoring bone mass, as the latter treatments can unintentionally trigger cancer development by undiscriminatingly promoting cell proliferation. One approach to circumvent this problem is through the development of novel chemical carriers to deliver drug agents specifically to bones. We have recently shown that carbon nanodots (C-dots) synthesized from carbon nanopowder can bind with high affinity and specificity to developing bones in the larval zebrafish. Larval bones, however, are physiologically different from adult bones in their growth, repair, and regeneration properties. Here we report that C-dots can bind to adult zebrafish bones and that this binding is highly specific to areas of appositional growth. C-dots deposition occurred within 30 minutes after delivery and was highly selective, with bones undergoing regeneration and repair showing higher levels of C-dots deposition than bones undergoing normal homeostatic turnover. Importantly, C-dots deposition did not interfere with bone regeneration or the animal’s health. Together, our results establish C-dots as a potential novel vehicle for the targeted delivery of drugs to treat adult bone disease. Taylor & Francis 2021-06-26 /pmc/articles/PMC8238062/ /pubmed/34176374 http://dx.doi.org/10.1080/10717544.2021.1938753 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
DuMez, Rachel
Miyanji, Esmail H.
Corado-Santiago, Lesly
Barrameda, Bryle
Zhou, Yiqun
Hettiarachchi, Sajini D.
Leblanc, Roger M.
Skromne, Isaac
In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery
title In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery
title_full In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery
title_fullStr In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery
title_full_unstemmed In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery
title_short In vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery
title_sort in vivo characterization of carbon dots–bone interactions: toward the development of bone-specific nanocarriers for drug delivery
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238062/
https://www.ncbi.nlm.nih.gov/pubmed/34176374
http://dx.doi.org/10.1080/10717544.2021.1938753
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