TY - JOUR
T1 - Biodistribution of iron oxide tattoo pigment
T2 - An experimental murine study
AU - Alsing, Kasper Køhler
AU - Johannesen, Helle Hjorth
AU - Hansen, Rasmus Hvass
AU - Mårtensson, Nina Løth
AU - Persson, Daniel Pergament
AU - Qvortrup, Klaus
AU - Wulf, Hans Christian
AU - Lerche, Catharina Margrethe
N1 - © 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2024/9
Y1 - 2024/9
N2 - Tattoo pigment is expected to migrate beyond the skin to regional lymph nodes and the liver. Modern tattoo ink commonly contains metals that may pose a clinical problem during MRI examinations. This study aimed to investigate the biodistribution of iron oxide pigment to internal organs in mice. Moreover, when exposed to a static magnetic field, we studied whether any reactions followed in the tattooed skin. Twenty-seven hairless C3.Cg-Hrhr/TifBomTac mice were included; 20 were tattooed with iron oxide ink in a rectangular 3 cm2 pattern; seven were controls. Ten of the tattooed mice were exposed to a 3 T MRI scanner's static magnetic field. Following euthanasia, evaluations of dissected organs involved MRI T2*-mapping, light microscopy (LM) and metal analysis. T2*-mapping measures the relaxation times of hydrogen nuclei in water and fat, which may be affected by neighbouring ferrimagnetic particles, thus enabling the detection of iron oxide particles in organs. Elemental analysis detected a significant level of metals in the tattooed skin compared to controls, but no skin reactions occurred when exposed to a 3 T static magnetic field. No disparity was observed in the liver samples with metal analysis. T2* mapping found no significant difference between the two groups. Only minute clusters of pigment particles were observed in the liver by LM. Our results demonstrate a minimal systemic distribution of the iron oxide pigments to the liver, whereas the kidney and brain were unaffected. The static magnetic field did not trigger skin reactions in magnetic tattoos but may induce image artefacts during MRI.
AB - Tattoo pigment is expected to migrate beyond the skin to regional lymph nodes and the liver. Modern tattoo ink commonly contains metals that may pose a clinical problem during MRI examinations. This study aimed to investigate the biodistribution of iron oxide pigment to internal organs in mice. Moreover, when exposed to a static magnetic field, we studied whether any reactions followed in the tattooed skin. Twenty-seven hairless C3.Cg-Hrhr/TifBomTac mice were included; 20 were tattooed with iron oxide ink in a rectangular 3 cm2 pattern; seven were controls. Ten of the tattooed mice were exposed to a 3 T MRI scanner's static magnetic field. Following euthanasia, evaluations of dissected organs involved MRI T2*-mapping, light microscopy (LM) and metal analysis. T2*-mapping measures the relaxation times of hydrogen nuclei in water and fat, which may be affected by neighbouring ferrimagnetic particles, thus enabling the detection of iron oxide particles in organs. Elemental analysis detected a significant level of metals in the tattooed skin compared to controls, but no skin reactions occurred when exposed to a 3 T static magnetic field. No disparity was observed in the liver samples with metal analysis. T2* mapping found no significant difference between the two groups. Only minute clusters of pigment particles were observed in the liver by LM. Our results demonstrate a minimal systemic distribution of the iron oxide pigments to the liver, whereas the kidney and brain were unaffected. The static magnetic field did not trigger skin reactions in magnetic tattoos but may induce image artefacts during MRI.
KW - Animals
KW - Tattooing
KW - Mice
KW - Ferric Compounds/pharmacokinetics
KW - Magnetic Resonance Imaging
KW - Tissue Distribution
KW - Liver/metabolism
KW - Skin/metabolism
KW - Mice, Hairless
KW - Coloring Agents/pharmacokinetics
KW - Ink
KW - Female
UR - http://www.scopus.com/inward/record.url?scp=85204512797&partnerID=8YFLogxK
U2 - 10.1111/exd.15183
DO - 10.1111/exd.15183
M3 - Journal article
C2 - 39304341
SN - 0906-6705
VL - 33
SP - e15183
JO - Experimental Dermatology
JF - Experimental Dermatology
IS - 9
M1 - e15183
ER -