Abstract

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.

Details

Title
Synchrotron-based ν-XRF mapping and μ-FTIR microscopy enable to look into the fate and effects of tattoo pigments in human skin
Author
Schreiver, Ines 1   VIAFID ORCID Logo  ; Hesse, Bernhard 2 ; Seim, Christian 3 ; Castillo-Michel, Hiram 2 ; Villanova, Julie 2 ; Laux, Peter 1 ; Dreiack, Nadine 1 ; Penning, Randolf 4 ; Tucoulou, Remi 2 ; Cotte, Marine 2 ; Luch, Andreas 1 

 German Federal Institute for Risk Assessment (BfR), Department of Chemical and Product Safety, Max-Dohrn-Strasse 8-10, Berlin, Germany 
 European Synchrotron Radiation Facility (ESRF), Grenoble, Cedex 9, France 
 Physikalisch-Technische Bundesanstalt, Department of X-ray Spectrometry, Abbestrasse 2-12, Berlin, Germany; Technische Universität Berlin, Institute for Optics and Atomic Physics, Berlin, Germany 
 Institute of Forensic Medicine, Ludwig-Maximilians University, Munich, Germany 
Pages
1-12
Publication year
2017
Publication date
Sep 2017
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1954332045
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.