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Synchrotron-based characterization of arthroprosthetic CoCrMo particles in human bone marrow
in
Biocompatibility
/ Biomedical materials
/ Bone composition
/ Bone implants
/ Bone marrow
/ Cell number
/ Chemical composition
/ Chromium
/ Cobalt
/ Data points
/ Exposure
/ Fluorescence
/ In vivo methods and tests
/ Inflammation
/ Materials science
/ Metal particles
/ Molybdenum
/ Orthopaedic implants
/ Particle size
/ Particle size distribution
/ Size distribution
/ Synchrotrons
/ Toxicity
/ X ray imagery
/ X-ray fluorescence
2022
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Synchrotron-based characterization of arthroprosthetic CoCrMo particles in human bone marrow
by
in
Biocompatibility
/ Biomedical materials
/ Bone composition
/ Bone implants
/ Bone marrow
/ Cell number
/ Chemical composition
/ Chromium
/ Cobalt
/ Data points
/ Exposure
/ Fluorescence
/ In vivo methods and tests
/ Inflammation
/ Materials science
/ Metal particles
/ Molybdenum
/ Orthopaedic implants
/ Particle size
/ Particle size distribution
/ Size distribution
/ Synchrotrons
/ Toxicity
/ X ray imagery
/ X-ray fluorescence
2022
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Synchrotron-based characterization of arthroprosthetic CoCrMo particles in human bone marrow
in
Biocompatibility
/ Biomedical materials
/ Bone composition
/ Bone implants
/ Bone marrow
/ Cell number
/ Chemical composition
/ Chromium
/ Cobalt
/ Data points
/ Exposure
/ Fluorescence
/ In vivo methods and tests
/ Inflammation
/ Materials science
/ Metal particles
/ Molybdenum
/ Orthopaedic implants
/ Particle size
/ Particle size distribution
/ Size distribution
/ Synchrotrons
/ Toxicity
/ X ray imagery
/ X-ray fluorescence
2022
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Synchrotron-based characterization of arthroprosthetic CoCrMo particles in human bone marrow
Journal Article
Synchrotron-based characterization of arthroprosthetic CoCrMo particles in human bone marrow
2022
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Overview
Particles released from cobalt-chromium-molybdenum (CoCrMo) alloys are considered common elicitors of chronic inflammatory adverse effects. There is a lack of data demonstrating particle numbers, size distribution and elemental composition of bone marrow resident particles which would allow for implementation of clinically relevant test strategies in bone marrow models at different degrees of exposure. The aim of this study was to investigate metal particle exposure in human periprosthetic bone marrow of three types of arthroplasty implants. Periprosthetic bone marrow sections from eight patients exposed to CoCrMo particles were analyzed via spatially resolved and synchrotron-based nanoscopic X-ray fluorescence imaging. These analyses revealed lognormal particle size distribution patterns predominantly towards the nanoscale. Analyses of particle numbers and normalization to bone marrow volume and bone marrow cell number indicated particle concentrations of up to 1 × 1011 particles/ml bone marrow or 2 × 104 particles/bone marrow cell, respectively. Analyses of elemental ratios of CoCrMo particles showed that particularly the particles’ Co content depends on particle size. The obtained data point towards Co release from arthroprosthetic particles in the course of dealloying and degradation processes of larger particles within periprosthetic bone marrow. This is the first study providing data based on metal particle analyses to be used for future in vitro and in vivo studies of possible toxic effects in human bone marrow following exposure to arthroprosthetic CoCrMo particles of different concentration, size, and elemental composition.
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