Disclosed is a method for perparation of
biological structure HAP / beta-TCP
tissue engineering bones, comprising 1.obtaining HAP by using
spongy bones of cattle
femoral bone lower part as
raw material, treating same by removing
bone marrow, lipid, and prorein, then rinsing,
drying, and high-temperature
processing, reacting HAP with NH4H2PO4, high-temperature
processing again, and obtaining a
biological structure HAP / beta-TCP material support frame; 2.isolating
bone marrow stroma stem cells
in vitro and seeding same in culture bottles, adding DMEM culture medium, cuturing at 37 DEG C with 5% CO2, changing the culture medium every 2-3 days, digesting cells with parenzyme as cells grow up to 90%, subculturing same, reserving same when the number of
bone marrow stroma reaches to 106-107 / ml; 3. rinsing biolofical structure HAP / beta-TCP material support frame with ultrasonic, dropping the subcultured cells on the support frame homogeneously, induced culturing same, obtaining said
biological structure HAP / beta-TCP
tissue engineering bone when cells fill internal void of support material. The
microstructure of disclosed biological structure HAP / beta-TCP
tissue engineering bone is completely analogical with
spongy bone, facilitates degradation of osteogenesis and support fame materials
in vivo which can be controlled, and so accelerating bone
recovery.