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Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation
Lipid and protein oxidation are well-known manifestations of free radical activity and oxidative stress. The current study investigated extermination of Leishmania tropica promastigotes induced by lipid and protein oxidation with reactive oxygen species produced by PEGylated metal-based nanoparticle...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898416/ https://www.ncbi.nlm.nih.gov/pubmed/27330288 http://dx.doi.org/10.2147/IJN.S105195 |
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author | Nadhman, Akhtar Khan, Malik Ihsanullah Nazir, Samina Khan, Momin Shahnaz, Gul Raza, Abida Shams, Dilawar Farhan Yasinzai, Masoom |
author_facet | Nadhman, Akhtar Khan, Malik Ihsanullah Nazir, Samina Khan, Momin Shahnaz, Gul Raza, Abida Shams, Dilawar Farhan Yasinzai, Masoom |
author_sort | Nadhman, Akhtar |
collection | PubMed |
description | Lipid and protein oxidation are well-known manifestations of free radical activity and oxidative stress. The current study investigated extermination of Leishmania tropica promastigotes induced by lipid and protein oxidation with reactive oxygen species produced by PEGylated metal-based nanoparticles. The synthesized photodynamic therapy-based doped and nondoped zinc oxide nanoparticles were activated in daylight that produced reactive oxygen species in the immediate environment. Lipid and protein oxidation did not occur in dark. The major lipid peroxidation derivatives comprised of conjugated dienes, lipid hydroperoxides, and malondialdehyde whereas water, ethane, methanol, and ethanol were found as the end products. Proteins were oxidized to carbonyls, hydroperoxides, and thiol degrading products. Interestingly, lipid hydroperoxides were produced by more than twofold of the protein hydroperoxides, indicating higher degradation of lipids compared to proteins. The in vitro evidence represented a significant contribution of the involvement of both lipid and protein oxidation in the annihilated antipromastigote effect of nanoparticles. |
format | Online Article Text |
id | pubmed-4898416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48984162016-06-21 Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation Nadhman, Akhtar Khan, Malik Ihsanullah Nazir, Samina Khan, Momin Shahnaz, Gul Raza, Abida Shams, Dilawar Farhan Yasinzai, Masoom Int J Nanomedicine Original Research Lipid and protein oxidation are well-known manifestations of free radical activity and oxidative stress. The current study investigated extermination of Leishmania tropica promastigotes induced by lipid and protein oxidation with reactive oxygen species produced by PEGylated metal-based nanoparticles. The synthesized photodynamic therapy-based doped and nondoped zinc oxide nanoparticles were activated in daylight that produced reactive oxygen species in the immediate environment. Lipid and protein oxidation did not occur in dark. The major lipid peroxidation derivatives comprised of conjugated dienes, lipid hydroperoxides, and malondialdehyde whereas water, ethane, methanol, and ethanol were found as the end products. Proteins were oxidized to carbonyls, hydroperoxides, and thiol degrading products. Interestingly, lipid hydroperoxides were produced by more than twofold of the protein hydroperoxides, indicating higher degradation of lipids compared to proteins. The in vitro evidence represented a significant contribution of the involvement of both lipid and protein oxidation in the annihilated antipromastigote effect of nanoparticles. Dove Medical Press 2016-05-31 /pmc/articles/PMC4898416/ /pubmed/27330288 http://dx.doi.org/10.2147/IJN.S105195 Text en © 2016 Nadhman et al. 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. |
spellingShingle | Original Research Nadhman, Akhtar Khan, Malik Ihsanullah Nazir, Samina Khan, Momin Shahnaz, Gul Raza, Abida Shams, Dilawar Farhan Yasinzai, Masoom Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation |
title | Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation |
title_full | Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation |
title_fullStr | Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation |
title_full_unstemmed | Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation |
title_short | Annihilation of Leishmania by daylight responsive ZnO nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation |
title_sort | annihilation of leishmania by daylight responsive zno nanoparticles: a temporal relationship of reactive oxygen species-induced lipid and protein oxidation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898416/ https://www.ncbi.nlm.nih.gov/pubmed/27330288 http://dx.doi.org/10.2147/IJN.S105195 |
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