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Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder: evaluations of phosphorus intercalation activity and cellular cytotoxicity
The patients with end-stage of renal disease (ESRD) need to take oral phosphate binder. Traditional phosphate binders may leave the disadvantage of aluminum intoxication or cardiac calcification. Herein, Mg-Fe-Cl hydrotalcite-like nanoplatelet (HTln) is for the first time characterized as potential...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007522/ https://www.ncbi.nlm.nih.gov/pubmed/27581184 http://dx.doi.org/10.1038/srep32458 |
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author | Lung, Yung-Feng Sun, Ying-Sui Lin, Chun-Kai Uan, Jun-Yen Huang, Her-Hsiung |
author_facet | Lung, Yung-Feng Sun, Ying-Sui Lin, Chun-Kai Uan, Jun-Yen Huang, Her-Hsiung |
author_sort | Lung, Yung-Feng |
collection | PubMed |
description | The patients with end-stage of renal disease (ESRD) need to take oral phosphate binder. Traditional phosphate binders may leave the disadvantage of aluminum intoxication or cardiac calcification. Herein, Mg-Fe-Cl hydrotalcite-like nanoplatelet (HTln) is for the first time characterized as potential oral phosphate binder, with respect to its phosphorus uptake capacity in cow milk and cellular cytotoxicity. A novel method was developed for synthesizing the Mg-Fe-Cl HTln powder in different Mg(2+): Fe(3+) ratios where the optimization was 2.8:1. Addition of 0.5 g Mg-Fe-Cl HTln in cow milk could reduce its phosphorus content by 40% in 30 min and by 65% in 90 min. In low pH environment, the Mg-Fe-Cl HTln could exhibit relatively high performance for uptaking phosphorus. During a 90 min reaction of the HTln in milk, no phosphorus restoration occurred. In-vitro cytotoxicity assay of Mg-Fe-Cl HTln revealed no potential cellular cytotoxicity. The cells that were cultured in the HTln extract-containing media were even more viable than cells that were cultured in extract-free media (blank control). The Mg-Fe-Cl HTln extract led to hundred ppm of Mg ion and some ppm of Fe ion in the media, should be a positive effect on the good cell viability. |
format | Online Article Text |
id | pubmed-5007522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50075222016-09-08 Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder: evaluations of phosphorus intercalation activity and cellular cytotoxicity Lung, Yung-Feng Sun, Ying-Sui Lin, Chun-Kai Uan, Jun-Yen Huang, Her-Hsiung Sci Rep Article The patients with end-stage of renal disease (ESRD) need to take oral phosphate binder. Traditional phosphate binders may leave the disadvantage of aluminum intoxication or cardiac calcification. Herein, Mg-Fe-Cl hydrotalcite-like nanoplatelet (HTln) is for the first time characterized as potential oral phosphate binder, with respect to its phosphorus uptake capacity in cow milk and cellular cytotoxicity. A novel method was developed for synthesizing the Mg-Fe-Cl HTln powder in different Mg(2+): Fe(3+) ratios where the optimization was 2.8:1. Addition of 0.5 g Mg-Fe-Cl HTln in cow milk could reduce its phosphorus content by 40% in 30 min and by 65% in 90 min. In low pH environment, the Mg-Fe-Cl HTln could exhibit relatively high performance for uptaking phosphorus. During a 90 min reaction of the HTln in milk, no phosphorus restoration occurred. In-vitro cytotoxicity assay of Mg-Fe-Cl HTln revealed no potential cellular cytotoxicity. The cells that were cultured in the HTln extract-containing media were even more viable than cells that were cultured in extract-free media (blank control). The Mg-Fe-Cl HTln extract led to hundred ppm of Mg ion and some ppm of Fe ion in the media, should be a positive effect on the good cell viability. Nature Publishing Group 2016-09-01 /pmc/articles/PMC5007522/ /pubmed/27581184 http://dx.doi.org/10.1038/srep32458 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lung, Yung-Feng Sun, Ying-Sui Lin, Chun-Kai Uan, Jun-Yen Huang, Her-Hsiung Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder: evaluations of phosphorus intercalation activity and cellular cytotoxicity |
title | Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder:
evaluations of phosphorus intercalation activity and cellular cytotoxicity |
title_full | Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder:
evaluations of phosphorus intercalation activity and cellular cytotoxicity |
title_fullStr | Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder:
evaluations of phosphorus intercalation activity and cellular cytotoxicity |
title_full_unstemmed | Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder:
evaluations of phosphorus intercalation activity and cellular cytotoxicity |
title_short | Synthesis of Mg-Fe-Cl hydrotalcite-like nanoplatelets as an oral phosphate binder:
evaluations of phosphorus intercalation activity and cellular cytotoxicity |
title_sort | synthesis of mg-fe-cl hydrotalcite-like nanoplatelets as an oral phosphate binder:
evaluations of phosphorus intercalation activity and cellular cytotoxicity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007522/ https://www.ncbi.nlm.nih.gov/pubmed/27581184 http://dx.doi.org/10.1038/srep32458 |
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