TY - JOUR
T1 - Fibroblast and osteoblast adhestion and morphology on calcium phosphate surfaces
AU - Richards, R. G.
AU - Frauchiger, V.
AU - Baxter, L. C.
AU - ap Gwynn, Iolo A.
AU - Textor, M.
N1 - Baxter, L. C., Frauchiger, V., Textor, M., ap Gwynn, I., Richards, R. G. (2002). Fibroblast and osteoblast adhestion and morphology on calcium phosphate surfaces. European Cells and Materials, 4, 1-17.
Sponsorship: KTI MedTech (grant number 4729.1), Robert Mathys Foundation and Stratec
Medical.
PY - 2002
Y1 - 2002
N2 - Implant loosening in bone fixation is an unresolved complication associated with internal fixation. It is generally accepted that this problem can be overcome by modifying the implant/bone interface for improved osseointegration.
This is achieved, in part, by hydroxyapatite (HA) or tricalcium phosphate coatings. Unfortunately, the benefits
of these coatings are constrained by not only the generally
low strength of their adhesion to the implant surface but
also the limited cohesion within their layers. Anodic Plasmachemical
treatment (APC) has been developed to incorporate
electrolytes and produce coatings with various
microtopographies and strong adhesion to implants. In this
in vitro study fibroblast and osteoblast morphologies and
adhesion to various substrates were evaluated using qualitative
and quantitative methods. The substrates were
Thermanox plastic and commercially pure titanium. The
latter were surface-treated using several different methods:
conventional anodisation, plasma spraying of HA and
anodic plasma-chemical (APC) treatment in an electrolyte
solution containing either calcium and phosphate (APCCaP)
or phosphoric acid (APC-P). Both osteoblasts and
fibroblasts showed extensive cell spreading, total cell area
and greatest amount of adhesion, with defined adhesion
patterns on the Thermanox plastic, anodised titanium, and
the two APC-CaP substrates. With fibroblasts, almost no
cell spreading and very low adhesion, was observed in cells
cultured on the APC-P and HA surfaces. The extent of cell
spreading correlated with the area of focal adhesions as
assessed by the amount of vinculin labelling. The
Thermanox plastic, anodised titanium, and the two APCCaP
substrates were the most cytocompatible substrates with
regard to this in vitro evaluation.
AB - Implant loosening in bone fixation is an unresolved complication associated with internal fixation. It is generally accepted that this problem can be overcome by modifying the implant/bone interface for improved osseointegration.
This is achieved, in part, by hydroxyapatite (HA) or tricalcium phosphate coatings. Unfortunately, the benefits
of these coatings are constrained by not only the generally
low strength of their adhesion to the implant surface but
also the limited cohesion within their layers. Anodic Plasmachemical
treatment (APC) has been developed to incorporate
electrolytes and produce coatings with various
microtopographies and strong adhesion to implants. In this
in vitro study fibroblast and osteoblast morphologies and
adhesion to various substrates were evaluated using qualitative
and quantitative methods. The substrates were
Thermanox plastic and commercially pure titanium. The
latter were surface-treated using several different methods:
conventional anodisation, plasma spraying of HA and
anodic plasma-chemical (APC) treatment in an electrolyte
solution containing either calcium and phosphate (APCCaP)
or phosphoric acid (APC-P). Both osteoblasts and
fibroblasts showed extensive cell spreading, total cell area
and greatest amount of adhesion, with defined adhesion
patterns on the Thermanox plastic, anodised titanium, and
the two APC-CaP substrates. With fibroblasts, almost no
cell spreading and very low adhesion, was observed in cells
cultured on the APC-P and HA surfaces. The extent of cell
spreading correlated with the area of focal adhesions as
assessed by the amount of vinculin labelling. The
Thermanox plastic, anodised titanium, and the two APCCaP
substrates were the most cytocompatible substrates with
regard to this in vitro evaluation.
M3 - Article
VL - 4
SP - 1
EP - 17
JO - European Cells and Materials
JF - European Cells and Materials
IS - 1-17
ER -