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Free radical formation from sonolysis of water in the presence of different gases
In the present study by applying electron spin resonance-spin trapping method, when a high frequency (1650 kHz) ultrasound was irradiated to water dissolved with different gas molecules (O(2), N(2), Ar, Ne, He, and H(2)) at 25°C of water bulk temperature, free radical generation pattern differed dep...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171683/ https://www.ncbi.nlm.nih.gov/pubmed/21980224 http://dx.doi.org/10.3164/jcbn.10-130 |
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author | Kohno, Masahiro Mokudai, Takayuki Ozawa, Toshihiko Niwano, Yoshimi |
author_facet | Kohno, Masahiro Mokudai, Takayuki Ozawa, Toshihiko Niwano, Yoshimi |
author_sort | Kohno, Masahiro |
collection | PubMed |
description | In the present study by applying electron spin resonance-spin trapping method, when a high frequency (1650 kHz) ultrasound was irradiated to water dissolved with different gas molecules (O(2), N(2), Ar, Ne, He, and H(2)) at 25°C of water bulk temperature, free radical generation pattern differed dependently on the dissolved gas molecules. Only (•)OH was detected in the O(2)-dissolved water sample, and the amount of the radical was much greater than that determined in any of other gas-dissolved water samples. One of the possible reasons to explain why the (•)H radical was not detected in the O(2)-dissolved water is that the (•)H reacts with O(2) to form (•)OOH. However, no electron spin resonance signals related to the adduct of not only 5,5-dimethyl-1-pyrroline-N-oxide but 5-(2,2-Dimethyl-1,3-propoxy cyclophosphoryl)-5-methyl-1-pyrroline N-oxide and (•)OOH were observed. In the H(2)-dissolved water, only (•)H was detected, suggesting that H(2) reduces or neutralizes (•)OH. In the N(2)-disolved water, both (•)OH and (•)H were detected at comparable level. In the water samples dissolved with rare gases (Ar, Ne, and He), the amount of (•)H was almost double as compared with that of (•)OH, and both (•)OH and (•)H yields increased in the order Ar > Ne > He. |
format | Online Article Text |
id | pubmed-3171683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-31716832011-10-06 Free radical formation from sonolysis of water in the presence of different gases Kohno, Masahiro Mokudai, Takayuki Ozawa, Toshihiko Niwano, Yoshimi J Clin Biochem Nutr Original Article In the present study by applying electron spin resonance-spin trapping method, when a high frequency (1650 kHz) ultrasound was irradiated to water dissolved with different gas molecules (O(2), N(2), Ar, Ne, He, and H(2)) at 25°C of water bulk temperature, free radical generation pattern differed dependently on the dissolved gas molecules. Only (•)OH was detected in the O(2)-dissolved water sample, and the amount of the radical was much greater than that determined in any of other gas-dissolved water samples. One of the possible reasons to explain why the (•)H radical was not detected in the O(2)-dissolved water is that the (•)H reacts with O(2) to form (•)OOH. However, no electron spin resonance signals related to the adduct of not only 5,5-dimethyl-1-pyrroline-N-oxide but 5-(2,2-Dimethyl-1,3-propoxy cyclophosphoryl)-5-methyl-1-pyrroline N-oxide and (•)OOH were observed. In the H(2)-dissolved water, only (•)H was detected, suggesting that H(2) reduces or neutralizes (•)OH. In the N(2)-disolved water, both (•)OH and (•)H were detected at comparable level. In the water samples dissolved with rare gases (Ar, Ne, and He), the amount of (•)H was almost double as compared with that of (•)OH, and both (•)OH and (•)H yields increased in the order Ar > Ne > He. the Society for Free Radical Research Japan 2011-09 2011-08-25 /pmc/articles/PMC3171683/ /pubmed/21980224 http://dx.doi.org/10.3164/jcbn.10-130 Text en Copyright © 2011 JCBN 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 work is properly cited. |
spellingShingle | Original Article Kohno, Masahiro Mokudai, Takayuki Ozawa, Toshihiko Niwano, Yoshimi Free radical formation from sonolysis of water in the presence of different gases |
title | Free radical formation from sonolysis of water in the presence of different gases |
title_full | Free radical formation from sonolysis of water in the presence of different gases |
title_fullStr | Free radical formation from sonolysis of water in the presence of different gases |
title_full_unstemmed | Free radical formation from sonolysis of water in the presence of different gases |
title_short | Free radical formation from sonolysis of water in the presence of different gases |
title_sort | free radical formation from sonolysis of water in the presence of different gases |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171683/ https://www.ncbi.nlm.nih.gov/pubmed/21980224 http://dx.doi.org/10.3164/jcbn.10-130 |
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