Bioactivation of alumina by surface modification: a possibility for improving the applicability of alumina in bone and oral repair

Objectives: In regenerative medicine, surface engineering of bioinert synthetic materials is often required in order to introduce bioactive species that can promote cell adhesion, proliferation, viability and enhanced ECM‐secretion functions. The aim of this work is to study cell interaction with al...

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Published in:Clinical oral implants research Vol. 20; no. 3; pp. 288 - 293
Main Authors: Bertazzo, S., Zambuzzi, W. F., Da Silva, H. A., Ferreira, C. V., Bertran, C. A.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-03-2009
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Summary:Objectives: In regenerative medicine, surface engineering of bioinert synthetic materials is often required in order to introduce bioactive species that can promote cell adhesion, proliferation, viability and enhanced ECM‐secretion functions. The aim of this work is to study cell interaction with alumina‐modified surfaces. Material and methods: In this work, chemical properties of alumina surface were changed by a reaction at the surface of alumina with low molecular weight dicarboxylic acid, which produced carboxyl groups. Results: These carboxyl groups were able to complex with Ca2+ on the surface, forming sites of precipitation for calcium phosphates that make alumina biocompatible, as indicated by cell culture of pre‐osteoblasts (MC3T3‐E1 cell line). Conclusions: The procedure presented in this work shows that the insertion of specific functional groups on the surface of alumina increases cell interaction with the surface of alumina. This knowledge can be important in oral science and orthopedics, for the construction of prosthesis.
Bibliography:ark:/67375/WNG-GN90JK1P-8
ArticleID:CLR1642
istex:B4016FC7A7A2D83F5BC24397704EC14C960CA779
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0905-7161
1600-0501
DOI:10.1111/j.1600-0501.2008.01642.x