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Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin

The increasing prevalence of tattoos provoked safety concerns with respect to particle distribution and effects inside the human body. We used skin and lymphatic tissues from human corpses to address local biokinetics by means of synchrotron X-ray fluorescence (XRF) techniques at both the micro (μ)...

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Autores principales: Schreiver, Ines, Hesse, Bernhard, Seim, Christian, Castillo-Michel, Hiram, Villanova, Julie, Laux, Peter, Dreiack, Nadine, Penning, Randolf, Tucoulou, Remi, Cotte, Marine, Luch, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595966/
https://www.ncbi.nlm.nih.gov/pubmed/28900193
http://dx.doi.org/10.1038/s41598-017-11721-z
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author Schreiver, Ines
Hesse, Bernhard
Seim, Christian
Castillo-Michel, Hiram
Villanova, Julie
Laux, Peter
Dreiack, Nadine
Penning, Randolf
Tucoulou, Remi
Cotte, Marine
Luch, Andreas
author_facet Schreiver, Ines
Hesse, Bernhard
Seim, Christian
Castillo-Michel, Hiram
Villanova, Julie
Laux, Peter
Dreiack, Nadine
Penning, Randolf
Tucoulou, Remi
Cotte, Marine
Luch, Andreas
author_sort Schreiver, Ines
collection PubMed
description The increasing prevalence of tattoos provoked safety concerns with respect to particle distribution and effects inside the human body. We used skin and lymphatic tissues from human corpses to address local biokinetics by means of synchrotron X-ray fluorescence (XRF) techniques at both the micro (μ) and nano (ν) scale. Additional advanced mass spectrometry-based methodology enabled to demonstrate simultaneous transport of organic pigments, heavy metals and titanium dioxide from skin to regional lymph nodes. Among these compounds, organic pigments displayed the broadest size range with smallest species preferentially reaching the lymph nodes. Using synchrotron μ-FTIR analysis we were also able to detect ultrastructural changes of the tissue adjacent to tattoo particles through altered amide I α-helix to β-sheet protein ratios and elevated lipid contents. Altogether we report strong evidence for both migration and long-term deposition of toxic elements and tattoo pigments as well as for conformational alterations of biomolecules that likely contribute to cutaneous inflammation and other adversities upon tattooing.
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spelling pubmed-55959662017-09-15 Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin Schreiver, Ines Hesse, Bernhard Seim, Christian Castillo-Michel, Hiram Villanova, Julie Laux, Peter Dreiack, Nadine Penning, Randolf Tucoulou, Remi Cotte, Marine Luch, Andreas Sci Rep Article The increasing prevalence of tattoos provoked safety concerns with respect to particle distribution and effects inside the human body. We used skin and lymphatic tissues from human corpses to address local biokinetics by means of synchrotron X-ray fluorescence (XRF) techniques at both the micro (μ) and nano (ν) scale. Additional advanced mass spectrometry-based methodology enabled to demonstrate simultaneous transport of organic pigments, heavy metals and titanium dioxide from skin to regional lymph nodes. Among these compounds, organic pigments displayed the broadest size range with smallest species preferentially reaching the lymph nodes. Using synchrotron μ-FTIR analysis we were also able to detect ultrastructural changes of the tissue adjacent to tattoo particles through altered amide I α-helix to β-sheet protein ratios and elevated lipid contents. Altogether we report strong evidence for both migration and long-term deposition of toxic elements and tattoo pigments as well as for conformational alterations of biomolecules that likely contribute to cutaneous inflammation and other adversities upon tattooing. Nature Publishing Group UK 2017-09-12 /pmc/articles/PMC5595966/ /pubmed/28900193 http://dx.doi.org/10.1038/s41598-017-11721-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Schreiver, Ines
Hesse, Bernhard
Seim, Christian
Castillo-Michel, Hiram
Villanova, Julie
Laux, Peter
Dreiack, Nadine
Penning, Randolf
Tucoulou, Remi
Cotte, Marine
Luch, Andreas
Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin
title Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin
title_full Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin
title_fullStr Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin
title_full_unstemmed Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin
title_short Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin
title_sort synchrotron-based ν-xrf mapping and μ-ftir microscopy enable to look into the fate and effects of tattoo pigments in human skin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595966/
https://www.ncbi.nlm.nih.gov/pubmed/28900193
http://dx.doi.org/10.1038/s41598-017-11721-z
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