Characterization of bovine hydroxyapatite–gelatin–gentamicin injectable bone substitutes as bone filler candidates for osteomyelitis
Osteomyelitis imposes a considerable burden on healthcare systems worldwide, and the development of effective injectable bone substitutes (IBSs) is vital to improving therapeutic outcomes. This study investigates the effect of varying bovine hydroxyapatite–gelatin (BHA–GEL) ratios on the physical characteristics, degradation rate, and gentamicin (GEN) release profile of IBS composites. Four formulations with BHA–GEL ratios of 75:25 (F1), 70:30 (F2), 65:35 (F3), and 60:40 (F4) were prepared and evaluated for pore diameter, functional group composition, setting time, injectability, degradation rate, and GEN release. Statistical analyses revealed that pore diameter differed significantly between F1 and F4 (p=0.013). All formulations exhibited setting times within the optimal range for IBS, with F1 demonstrating a significantly shorter setting time than F2, F3, and F4 (p<0.05). Injectability exceeded 96% across all groups, with no significant differences. The degradation rate was significantly different between F1 and F4 (p=0.033). GEN release showed no statistical difference among formulations but followed a trend of higher release with increasing gelatin content. These findings demonstrate that the BHA–GEL ratio significantly influences setting time, pore diameter (between F1 and F4), and degradation rate (between F1 and F4), while having minimal effects on injectability and GEN release, suggesting potential as bone filler candidates.
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