Papers by Author: Byung Hyun Lee

Abstract: We developed new calcium phosphate bone substitute material, amorphous calcium polyphosphate. The new material is synthesized by a cement-like slif-setting reaction with calcium phosphate glass, basic materials and water. In this study, we prepared with CPG, Na2CO3 and NaOH solution. When they are mixed together, amorphous phase was precipitated. The precipitated amorphous phase consisted of polyphosphate chains condensed with Na ions released from Na2CO3 and NaOH. When the amorphous calcium polyphosphate dissolves, inorganic polyphosphates are released into the medium. The inorganic polyphosphates as the dissolution product inducted the calcification of the osteoblast cells. Therefore, in animal test, the new bone formation in rat calvarial defects treated with the new material was significantly higher than sham-surgery control group, especially in the initial stage. The amorphous calcium polyphosphate was biocompatible and bioresorbable and promoted the new bone formation.

Abstract: A numerous techniques have been applied to fabricate three-dimensional scaffolds of high porosity and surface area. And X-ray micro computed tomography can be used studying the architecture of scaffold. In this study, we fabricated three-dimensional macroporous scaffold by polymeric sponge method using calcium phosphate glass. Calcium phosphate glass slurry was prepared by dissolving the glass powder in water polyvinyl alcohol, polyethylene glycol and dimethyl formamide. Reticulated polyurethane sponges were used as a template and were coated with the prepared slurry by infiltration technique several times. Sintering at 950oC exhibited dense microstructure as well as entire elimination of organic additives. By repeating the coating and sintering process, it was possible to decrease the pore size and be thick the strut of the structure. The unique feature of the micro computed tomography is that the three dimensions computed reconstruction can be sliced along any direction to gain accurate information on the internal geometric properties and structural parameters of scaffold. Porosity, surface area per unit volume and mean thickness of strut were evaluated through imaging and computer software of scaffold scan data.

Abstract: The objective of this study was to produce a macroporous hydroxyapatite(HA) scaffold with high strength by controlling the size of HA particles as well as cooling rate from the sintering temperature. Macroporous polyurethane sponge was employed as template to manufacture the macroporous HA scaffolds. Particle sizes of HA powders selected in this study were 4 µm and 7 µm. They were dispersed in distilled water with organic additives and infiltrated into polyurethane sponge. After drying and sintering at 1300oC, cooled down to room temperature slowly to prevent microcracking either 1oC/min or 3oC/min. Density, porosity and compressive strength were measured with different particle size and cooling rate. Both density and compressive strength were increased with decreasing particle size or cooling rate, while porosity was not related to.

Abstract: In preliminary ageing test, the cement using only calcium phosphate glass as power phase cracked with 1 day in simulated body fluid because of high dissolution rate of the cement. We added 30 wt% of either β-TCP or HA to 70 wt% calcium phosphate glass as powder phase to control the dissolution rate of the cement and performed in vitro ageing test in simulated body fluid by dynamic protocol as well as static protocol to confirm the possibility of controlling. Adding either β-TCP or HA to the cement increases the setting time and decreases the compressive strength. In dynamic assay, the pH of extract is maintained over 7. However, pH decreased to around 5 in static assay. Therefore, weight loss by static protocol continuously increased for 14 days, while weight loss by dynamic protocol almost saturated. In XRD patterns of ageing cements, CaO peaks appeared. CaO peak was maximized most lately in dynamic assay of the cement adding HA and within 7 days, the cement adding HA showed higher weight loss. It is indicated that CaO formed in surface of the cement hinder the dissolution of the cement. In addition, compressive strength increased when the CaO peak was maximized.

Abstract: The mixed pastes of binary calcium phosphate glass with Ca/P ratio of 0.6 and distilled water were set after about 4 hr, while never set when calcium phosphate glass with Ca/P lower than 0.5. Their compressive strength was ranged from 16.0 to 23.3 MPa. When Na2HPO4 solution was used instead of distilled water as liquid phase, the setting time became drastically much shorter. As the mole concentration of Na2HPO4 solution increased from 0.25 M to 2 M, setting time was shortened to 35 min from almost 3 hr, but compressive strength decreased from 28.8 MPa to 13.2 MPa. At constant mole concentration, as the mass ratio of a powder to liquid ratio increased, setting time was shortened and maximum compressive strength was measured when a powder/liquid ratio was 2.5. However, no crystallized phases were detected either during setting or after complete setting. The XRD , FT-IR and SEM examinations indicated that calcium phosphate glass dissolved and then glass phase precipitated again. We concluded, therefore, that Na2HPO4 just affected the kinetics of dissolution and precipitation of CPG. The mechanism of hardening has yet to be studied.