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In vivo comparative biokinetics and biocompatibility of titanium and zirconium microparticles
Journal of biomedical materials research. Part A, 2011-09, Vol.98A (4), p.604-613
Olmedo, Daniel G.
Tasat, Deborah R.
Evelson, Pablo
Rebagliatti, Raúl
Guglielmotti, María B.
Cabrini, Rómulo L.
2011
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Olmedo, Daniel G.
Tasat, Deborah R.
Evelson, Pablo
Rebagliatti, Raúl
Guglielmotti, María B.
Cabrini, Rómulo L.
Titel
In vivo comparative biokinetics and biocompatibility of titanium and zirconium microparticles
Ist Teil von
Journal of biomedical materials research. Part A, 2011-09, Vol.98A (4), p.604-613
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2011
Quelle
MEDLINE
Beschreibungen/Notizen
Titanium and zirconium are biomaterials that present a layer of titanium dioxide (TiO2) or zirconium dioxide (ZrO2). As a result of corrosion, microparticles can be released into the bioenvironment, and their effect on tissues is seemingly associated with differences in the physicochemical properties of these metals. The aim of this study was to perform a long‐term evaluation of the distribution, destination, and potential risk of TiO2 and ZrO2 microparticles that might result from the corrosion process. Wistar rats were i.p. injected with an equal dose of either TiO2 or ZrO2 suspension. The following end‐points were evaluated at 3, 6, and 18 months: (a) the presence of particles in blood cells and liver and lung tissue, (b) Ti and Zr deposit quantitation, (c) oxidant–antioxidant balance in tissues, and (d) O2− generation in alveolar macrophages. Ti and Zr particles were detected in blood mononuclear cells and in organ parenchyma. At equal doses and times postadministration, Ti content in organs was consistently higher than Zr content. Ti elicited a significant increase in O2− generation in the lung compared to Zr. The consumption of antioxidant enzymes was greater in the Ti than in the Zr group. The present study shows that the biokinetics of TiO2 and ZrO2 depends on particle size, shape, and/or crystal structure. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part A:, 2011.
Sprache
Englisch
Identifikatoren
ISSN: 1549-3296, 1552-4965
eISSN: 1552-4965
DOI: 10.1002/jbm.a.33145
Titel-ID: cdi_proquest_miscellaneous_893266296
Format
–
Schlagworte
Animals
,
Antioxidants - metabolism
,
Biocompatible Materials - chemistry
,
Biocompatible Materials - metabolism
,
biokinetics
,
Biological and medical sciences
,
Biomarkers - metabolism
,
Corrosion
,
macrophages
,
Macrophages, Alveolar - cytology
,
Macrophages, Alveolar - metabolism
,
Male
,
Materials Testing
,
Medical sciences
,
microparticles
,
Oxidation-Reduction
,
Oxidative Stress
,
Particle Size
,
Rats
,
Rats, Wistar
,
Superoxides - metabolism
,
Surface Properties
,
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
,
Technology. Biomaterials. Equipments
,
Thiobarbituric Acid Reactive Substances - metabolism
,
Tissue Distribution
,
titanium
,
Titanium - chemistry
,
Titanium - metabolism
,
zirconium
,
Zirconium - chemistry
,
Zirconium - metabolism
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