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Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage

PURPOSE: Vitamin D3 is useful for the treatment of peritoneal dialysis (PD)-related peritoneal damage, but its side effects, such as hypercalcemia and vascular calcification, limit its applicability. Thus, we developed vitamin D-loaded magnetic nanoparticles (MNPs) and determined their therapeutic e...

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Autores principales: Cheng, Fong-Yu, Chiou, Yuan-Yow, Hung, Shih-Yuan, Lin, Tsun-Mei, Wang, Hao-Kuang, Lin, Chi-Wei, Liou, Hung-Hsiang, Chang, Min-Yu, Wang, Hsi-Hao, Lee, Yi-Che
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959003/
https://www.ncbi.nlm.nih.gov/pubmed/33731995
http://dx.doi.org/10.2147/IJN.S291001
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author Cheng, Fong-Yu
Chiou, Yuan-Yow
Hung, Shih-Yuan
Lin, Tsun-Mei
Wang, Hao-Kuang
Lin, Chi-Wei
Liou, Hung-Hsiang
Chang, Min-Yu
Wang, Hsi-Hao
Lee, Yi-Che
author_facet Cheng, Fong-Yu
Chiou, Yuan-Yow
Hung, Shih-Yuan
Lin, Tsun-Mei
Wang, Hao-Kuang
Lin, Chi-Wei
Liou, Hung-Hsiang
Chang, Min-Yu
Wang, Hsi-Hao
Lee, Yi-Che
author_sort Cheng, Fong-Yu
collection PubMed
description PURPOSE: Vitamin D3 is useful for the treatment of peritoneal dialysis (PD)-related peritoneal damage, but its side effects, such as hypercalcemia and vascular calcification, limit its applicability. Thus, we developed vitamin D-loaded magnetic nanoparticles (MNPs) and determined their therapeutic efficacy and side effects in vivo. MATERIALS AND METHODS: Alginate-modified MNPs were combined with 1α, 25 (OH)(2)D(3) to generate vitamin D-loaded nanoparticles. The particles were conjugated with an antibody against peritoneum-glycoprotein M6A (GPM6A). The particles’ ability to target the peritoneum was examined following intraperitoneal administration to mice and by monitoring their bio-distribution. We also established a PD animal model to determine the therapeutic and side effects of vitamin D-loaded MNPs in vivo. RESULTS: Vitamin D-loaded MNPs targeted the peritoneum better than vitamin D3, and had the same therapeutic effect as vitamin D3 in ameliorating peritoneal fibrosis and functional deterioration in a PD animal model. Most importantly, the particles reduced the side effects of vitamin D3, such as hypercalcemia and body weight loss, in mice. CONCLUSION: Vitamin D-loaded MNPs could be an ideal future therapeutic option to treat PD-related peritoneal damage.
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spelling pubmed-79590032021-03-16 Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage Cheng, Fong-Yu Chiou, Yuan-Yow Hung, Shih-Yuan Lin, Tsun-Mei Wang, Hao-Kuang Lin, Chi-Wei Liou, Hung-Hsiang Chang, Min-Yu Wang, Hsi-Hao Lee, Yi-Che Int J Nanomedicine Original Research PURPOSE: Vitamin D3 is useful for the treatment of peritoneal dialysis (PD)-related peritoneal damage, but its side effects, such as hypercalcemia and vascular calcification, limit its applicability. Thus, we developed vitamin D-loaded magnetic nanoparticles (MNPs) and determined their therapeutic efficacy and side effects in vivo. MATERIALS AND METHODS: Alginate-modified MNPs were combined with 1α, 25 (OH)(2)D(3) to generate vitamin D-loaded nanoparticles. The particles were conjugated with an antibody against peritoneum-glycoprotein M6A (GPM6A). The particles’ ability to target the peritoneum was examined following intraperitoneal administration to mice and by monitoring their bio-distribution. We also established a PD animal model to determine the therapeutic and side effects of vitamin D-loaded MNPs in vivo. RESULTS: Vitamin D-loaded MNPs targeted the peritoneum better than vitamin D3, and had the same therapeutic effect as vitamin D3 in ameliorating peritoneal fibrosis and functional deterioration in a PD animal model. Most importantly, the particles reduced the side effects of vitamin D3, such as hypercalcemia and body weight loss, in mice. CONCLUSION: Vitamin D-loaded MNPs could be an ideal future therapeutic option to treat PD-related peritoneal damage. Dove 2021-03-11 /pmc/articles/PMC7959003/ /pubmed/33731995 http://dx.doi.org/10.2147/IJN.S291001 Text en © 2021 Cheng et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Cheng, Fong-Yu
Chiou, Yuan-Yow
Hung, Shih-Yuan
Lin, Tsun-Mei
Wang, Hao-Kuang
Lin, Chi-Wei
Liou, Hung-Hsiang
Chang, Min-Yu
Wang, Hsi-Hao
Lee, Yi-Che
Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage
title Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage
title_full Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage
title_fullStr Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage
title_full_unstemmed Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage
title_short Novel Application of Magnetite Nanoparticle-Mediated Vitamin D3 Delivery for Peritoneal Dialysis-Related Peritoneal Damage
title_sort novel application of magnetite nanoparticle-mediated vitamin d3 delivery for peritoneal dialysis-related peritoneal damage
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959003/
https://www.ncbi.nlm.nih.gov/pubmed/33731995
http://dx.doi.org/10.2147/IJN.S291001
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