Our objective was to observe the biodegradable and osteogenic properties of magnesium
scaffolding under in vivo conditions. Twelve 6-month-old male New
Zealand white rabbits were randomly divided into two groups. The chosen operation
site was the femoral condyle on the right side. The experimental group was implanted
with porous magnesium scaffolds, while the control group was implanted with
hydroxyapatite scaffolds. X-ray and blood tests, which included serum magnesium,
alanine aminotransferase (ALT), creatinine (CREA), and blood urea nitrogen (BUN) were
performed serially at 1, 2, and 3 weeks, and 1, 2, and 3 months. All rabbits were
killed 3 months postoperatively, and the heart, kidney, spleen, and liver were
analyzed with hematoxylin and eosin (HE) staining. The bone samples were subjected to
microcomputed tomography scanning (micro-CT) and hard tissue biopsy. SPSS 13.0 (USA)
was used for data analysis, and values of P<0.05 were considered to be
significant. Bubbles appeared in the X-ray of the experimental group after 2 weeks,
whereas there was no gas in the control group. There were no statistical differences
for the serum magnesium concentrations, ALT, BUN, and CREA between the two groups
(P>0.05). All HE-stained slices were normal, which suggested good biocompatibility
of the scaffold. Micro-CT showed that magnesium scaffolds degraded mainly from the
outside to inside, and new bone was ingrown following the degradation of magnesium
scaffolds. The hydroxyapatite scaffold was not degraded and had fewer osteoblasts
scattered on its surface. There was a significant difference in the new bone
formation and scaffold bioabsorption between the two groups (9.29±1.27
vs 1.40±0.49 and 7.80±0.50 vs 0.00±0.00
mm3, respectively; P<0.05). The magnesium scaffold performed well in
degradation and osteogenesis, and is a promising material for orthopedics.