Literature DB >> 15348344

In vivo/ex vivo cellular interactions with titanium and copper.

F Suska1, M Källtorp, M Esposito, C Gretzer, P Tengvall, P Thomsen.   

Abstract

Machined, commercially pure titanium (Ti) disks were coated with approximately 400 nm copper (Cu) by physical vapor deposition or left uncoated. The kinetics of inflammatory cell recruitment, distribution and viability was evaluated around Ti, Cu, and in sham sites after 1, 3, 12, 18, 24, and 48 h in a rat subcutaneous (s.c.) model. Further analysis of the cells on implant surfaces was performed by ex vivo incubation of the disks. Ti and Cu stimulated an increased recruitment of inflammatory cells in comparison with sham sites. A markedly higher amount of cells, predominantly polymorpho-nuclear granulocytes (PMN), was detected around Cu after 18 h and onwards. More cells were found at the implant surfaces than in the surrounding exudates after 18 h. The total amount of lactate dehydrogenase (LDH), an indicator of plasma membrane injury, was higher in Cu exudates after 18 h in comparison with Ti and sham. In contrast, no differences in the proportion of dead cells (trypan blue dye uptake) were detected in the exudates. Further, LDH levels were higher around Ti than Cu during the initial 18 h of ex vivo incubation. The results of this study indicate that the early inflammatory process associated with a cytotoxic material in soft tissues is largely attributed to the induction of a markedly strong and prolonged chemotactic response. In contrast, this process is characterized by a higher amount of inflammatory cells around a biocompatible material than in sham sites, but with a transient course and total LDH similar to sham sites. Copyright 2001 Kluwer Academic Publishers

Entities:  

Year:  2001        PMID: 15348344     DOI: 10.1023/a:1012844612753

Source DB:  PubMed          Journal:  J Mater Sci Mater Med        ISSN: 0957-4530            Impact factor:   3.896


  38 in total

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Journal:  Dent Mater       Date:  1993-03       Impact factor: 5.304

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Authors:  A McNamara; D F Williams
Journal:  Biomaterials       Date:  1981-01       Impact factor: 12.479

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Journal:  J Natl Cancer Inst       Date:  1982-11       Impact factor: 13.506

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Authors:  G Patstone; P Maher
Journal:  J Biol Chem       Date:  1996-02-16       Impact factor: 5.157

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