BONE-FORMATION BY 3-DIMENSIONAL STROMAL OSTEOBLAST CULTURE IN BIODEGRADABLE POLYMER SCAFFOLDS

Bone formation was investigated in vitro by culturing stromal osteobla sts in three-dimensional (3-D), biodegradable poly(DL-lactic-co-glycol ic acid) foams. Three polymer foam pore sizes, ranging from 150-300, 3 00-500, and 500-710 mu m, and two different cell seeding densities, 6. 83 x 10(5) cells/cm(2) and 22.1 x 10(5) cells/cm(2), were examined ove r a 56-day culture period. The polymer foams supported the proliferati on of seeded osteoblasts as well as their differentiated function, as demonstrated by high alkaline phosphatase activity and deposition of a mineralized matrix by the cells. Cell number, alkaline phosphatase ac tivity, and mineral deposition increased significantly over time for a ll the polymer foams. Osteoblast foam constructs created by seeding 6. 83 x 10(5) cells/cm(2) on foams with 300-500 mu m pores resulted in a cell density of 4.63 x 10(5) cells/cm(2) after 1 day in culture; they had alkaline phosphatase activities of 4.28 x 10(-7) and 2.91 x 10(-6) mu mol/cell/min on Days 7 and 28, respectively; and they had a cell d ensity that increased to 18.7 x 10(5) cells/cm(2) by Day 56. For the s ame constructs, the mineralized matrix reached a maximum penetration d epth of 240 mu m from the top surface of the foam and a value of 0.083 mm for mineralized tissue volume per unit of cross sectional area. Se eding density was an important parameter for the constructs, but pore size over the range tested did not affect cell proliferation or functi on. This study suggests the feasibility of using poly(a-hydroxy ester) foams as scaffolding materials for the transplantation of autogenous osteoblasts to regenerate bone tissue. (C) 1997 John Wiley & Sons, Inc .