HA ; PLGA ; injectable ; antibiotic ; tetracycline
Abstract
This study investigated the possibility of an injectable bone substitute consisting of methylcellulose
aqueous solutions and poly lactide-co-glycolide acid/hydroxyapatite (PLGA/HA) composite microspheres containing
sustained releasing antibiotics. HA nanoparticles were synthesized by coprecipitation. PLGA/HA composite
microspheres were prepared by oil-in-water emulsion/solvent evaporation with tetracycline. They were mixed with
a 2% (w/v) aqueous solution of methylcellulose. The particle size of the composite microspheres increased linearly
with increasing PLGA concentration from 17.8±4.5 to 185.4±29.5 μm. As the size of PLGA/HA composite microspheres
increased, the content of tetracycline increased from 0.8% to 70.3%. The release rate of tetracycline
decreased with increasing size of the composite microspheres. Tetracycline exhibited a burst release with nearly
100% escape within 24 hrs when the PLGA concentration was less than 20%. Sustained continuous release until 2
weeks when PLGA content was 20%. The gelation temperature of methylcellulose can be adjusted to normal body
temperature when NaCl content exceeds 5%. PLGA/HA composite microspheres mixed with a methylcellulose
aqueous solution was easily and completely ejected through an 18G needle when the mixing ratio was below 100%.