INEB
INEB
TitleThe influence of functional groups of self-assembled monolayers on fibrous capsule formation and cell recruitment
Publication TypeJournal Article
2006
AuthorsBarbosa, JN, Madureira, P, Barbosa, MA, Águas, AP
JournalJournal of Biomedical Materials Research - Part AJ. Biomed. Mater. Res. Part A
Volume76
Issue4
Pagination737 - 743
Date Published2006///
15493296 (ISSN)
animal, animal cell, animal experiment, animal model, animal tissue, Animals, article, Bagg albino mouse, Biocompatible Materials, biomaterial, chemistry, controlled study, flow cytometry, functional group, gold, histology, implantation, Inflammation, male, Mice, Mice, Inbred BALB C, Monolayers, mouse, nonhuman, Self assembly, Self-assembled monolayers, Sulfhydryl Compounds, Surface chemistry, thiol derivative, tissue reaction, Tissue responses
The contribution of the surface chemistry of an implant to the thickness of the fibrous capsule formed after implantation was herein investigated. For that, self-assembled monolayers (SAMs) of alkanethiols on gold with different terminal functional groups (COOH, OH, and CH 3) were used. These surfaces were implanted in subcutaneous air pouches of BALB/c mice and the ensuing fibrous capsules were evaluated and compared with the initial inflammatory response caused by the implant. The thickness of the fibrous capsules that are under organization around the implant was measured 1 week after implantation by histology. Inflammatory exudates were collected from the air pouches 24 h after the implantation of SAMs and were analyzed by flow cytometry. A significant increase in the thickness of fibrous capsules was seen around implanted CH 3-terminated SAMs, and also in gold surfaces, in comparison with the air pouch wall of sham-operated mice and of COOH- and OH-covered SAMs. The CH 3-coated implants also recruited higher numbers of inflammatory cells; this enhancement involved a significant number of Mac-1 + cells. Our data indicate that implant surfaces coated with CH 3 induce thick fibrous capsules and this may be the result of the stronger inflammatory effect of CH 3 in comparison with COOH or OH chemical groups. © 2005 Wiley Periodicals, Inc.
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