B. Saad et al., DegraPol-Foam: A degradable and highly porous polyesterurethane foam as a new substrate for bone formation, ARTIF ORGAN, 24(12), 2000, pp. 939-945
Bone morphogenetic protein (BMP) is known to require a suitable carrier to
induce ectopic bone formation in vivo. To evaluate the suitability of Degra
Pol-foam, a degradable, elastic, and highly porous polyesterurethane foam a
s carrier for BMP-induced bone formation, a fraction containing all the act
ive BMPs (BMP cocktail) was combined with DegraPol-foam and implanted subcu
taneously into rats. DegraPol-BMP scaffolds were found to induce osteogenes
is 2 weeks after implantation as evidenced by morphological and biochemical
observations. In addition, the osteoblast-compatibility of DegraPol-foam w
as examined here. In vitro, primary rat osteoblasts and osteoblasts from th
e human cell line (HFO1) attached and proliferated preferentially on the su
rface of the DegraPol-foam. Both cell types exhibited relatively high attac
hment and low doubling time that resulted in a confluent cell multilayer wi
th spindle-shaped morphology on the surface of the foam. Osteoblasts produc
ed high concentrations of collagen type I and osteocalcin, and expressed in
creasing levels of alkaline phosphatase (ALP) activity. Taken collectively,
both osteoblasts from rat tibia and from the human cell line HFO1 showed h
igh cell attachment and growth, and preserved their phenotype. The geometri
cal structure of DegraPol is a suitable carrier for BMP for the induction o
f bone formation.