Source abstract
Abstract
The strategies used to associate peptide arginylglycylaspartic acid (RGD) with calcium phosphate grafts to enhance cell–biomaterial interactions have been controversial in the literature. Several works have demonstrated that RGD-functionalized hydroxyapatite (HA) surfaces improve cell adhesion, whereas others claim that RGD-loaded HA has an inhibitory effect when serum is present in the biological medium. To investigate such contradictory results, we associated RGD with the HA surface using physical adsorption and chemical bonding methods and evaluated the cell adhesion and spreading in pre-osteoblasts culture with and without fetal bovine serum (FBS). The effect of functionalization methods on the physicochemical characteristics of both surfaces was analyzed using multiscale techniques. Adsorption assays of serum allowed us to estimate the impact of the association method on the HA surface’s reactivity. Physically adsorbed RGD did not increase the number of adhered cells due to the weak interactions between the peptide and the surface. Although chemical binding stabilizes RGD on the HA, the functionalization procedure covered the surface with molecules such as (3-aminopropyl)triethoxysilane (APTEs) and carbodiimide, changing the surface’s chemical activity. Serum protein adsorption decreased by 90%, revealing a significant reduction in the surface interactions with molecules of the biological medium. The present study’s findings showed that the RGD’s physical association with HA did not improve cell adhesion and that this phenomenon is highly dependent on the presence of serum proteins.
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Affiliations
Coordenação de Matéria Condensada, Física Aplicada e Nanociência (COMAN), Centro Brasileiro de Pesquisas Físicas (CBPF), Rio de Janeiro 22290-180, Brazil
Metallurgical and Materials Engineering, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21945-970, Brazil
Brazilian National Institute of Metrology, Standardization and Industrial Quality, Rio de Janeiro 20261-232, Brazil
Department of Clinical and Translational Research, Tufts University School of Dental Medicine, Boston, MA 02111, USA
Department of Medical, Oral and Biotechnological Sciences, Center for Advanced Studies and Technology (CAST), “G. d’Annunzio” University of Chieti-Pescara, 66100 Chieti, Italy
School of Dentistry, Saint Camillus International University of Health and Medical Sciences, 00131 Rome, Italy
Cell and Molecular Biology Department, Institute of Biology, Fluminense Federal University, Niteroi 24220-900, Brazil