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Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes
Uraemic toxins—creatol and N-methylguanidine—are generated in conversion of creatinine in water in the presence of various forms of carbon such as fullerene C(60), carbon-encapsulated magnetic nanoparticles, and multiwalled carbon nanotubes and oxygen. The conversion degree for creatinine was differ...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775425/ https://www.ncbi.nlm.nih.gov/pubmed/24078905 http://dx.doi.org/10.1155/2013/168512 |
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author | Popławska, Magdalena Krawczyk, Hanna |
author_facet | Popławska, Magdalena Krawczyk, Hanna |
author_sort | Popławska, Magdalena |
collection | PubMed |
description | Uraemic toxins—creatol and N-methylguanidine—are generated in conversion of creatinine in water in the presence of various forms of carbon such as fullerene C(60), carbon-encapsulated magnetic nanoparticles, and multiwalled carbon nanotubes and oxygen. The conversion degree for creatinine was different for fullerene C(60), CEMNPs, and MWCNTs and was 9% (3.6% creatol, 5.4% N-methylguanidine), 35% (12% creatol, 23% N-methylguanidine), and 75% (16% creatol, 59% N-methylguanidine), respectively. |
format | Online Article Text |
id | pubmed-3775425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37754252013-09-29 Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes Popławska, Magdalena Krawczyk, Hanna Biomed Res Int Research Article Uraemic toxins—creatol and N-methylguanidine—are generated in conversion of creatinine in water in the presence of various forms of carbon such as fullerene C(60), carbon-encapsulated magnetic nanoparticles, and multiwalled carbon nanotubes and oxygen. The conversion degree for creatinine was different for fullerene C(60), CEMNPs, and MWCNTs and was 9% (3.6% creatol, 5.4% N-methylguanidine), 35% (12% creatol, 23% N-methylguanidine), and 75% (16% creatol, 59% N-methylguanidine), respectively. Hindawi Publishing Corporation 2013 2013-09-02 /pmc/articles/PMC3775425/ /pubmed/24078905 http://dx.doi.org/10.1155/2013/168512 Text en Copyright © 2013 M. Popławska and H. Krawczyk. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Popławska, Magdalena Krawczyk, Hanna Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes |
title | Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes |
title_full | Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes |
title_fullStr | Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes |
title_full_unstemmed | Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes |
title_short | Uraemic Toxins Generated in the Presence of Fullerene C(60), Carbon-Encapsulated Magnetic Nanoparticles, and Multiwalled Carbon Nanotubes |
title_sort | uraemic toxins generated in the presence of fullerene c(60), carbon-encapsulated magnetic nanoparticles, and multiwalled carbon nanotubes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775425/ https://www.ncbi.nlm.nih.gov/pubmed/24078905 http://dx.doi.org/10.1155/2013/168512 |
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