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. 2021 Aug 24;32(9):107.
doi: 10.1007/s10856-021-06587-7.

Bone induction and defect repair by true bone ceramics incorporated with rhBMP-2 and Sr

Affiliations

Bone induction and defect repair by true bone ceramics incorporated with rhBMP-2 and Sr

Chunli Zhang et al. J Mater Sci Mater Med. .

Abstract

Objective: To study the bone induction and defect repair of true bone ceramics (TBC) combined with rhBMP-2 and Sr.

Methods: MC3T3-E1 cells were used to evaluate the bioactivity of the composite. Cell proliferation activity was detected by CCK-8, ALP activity was detected by p-nitrophenyl phosphate (PNPP), and the differences of material surface topography were observed by scanning electron microscopy (SEM). Bone induction was verified by the implantation in nude mice. The rabbit femoral condyle defect model was achieved to verify the bone defect repair ability of the material.

Results: SEM results showed nearly the same surface morphology and cell proliferation quantified by CCK-8 showed that compared with TBC, both TBC&Sr and TBC&BMP-2&Sr had a significant promoting effect (P < 0.05). ALP activity result showed that the ALP activity of TBC&BMP-2&Sr was significantly higher than that of TBC alone (P < 0.05). The bone induction result showed that TBC&Sr had a small amount of new bone formation, and the new bone area was only 2.5 ± 0.11%. The bone induction activity of TBC&BMP-2&Sr was the highest, the new bone area was up to 75.36 ± 4.21%. Histological result of bone defect repair showed that TBC&BMP-2&Sr was also the highest, the new bone area was up to 72.42 ± 3.14%. The repair effect of TBC& BMP-2 was second, and better than that of TBC&Sr.

Conclusion: TBC combined with rhBMP-2 and Sr had the good bioactivity, obvious bone conduction and bone defect repair performance, laying the foundation of clinical application potentially.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
A The surface topography of the bone material observed by scanning electron microscopy (SEM) (100×); B Effects of four materials on the MC3T3-E1 proliferation (n = 4); C Effects of four materials on the ALP activity (n = 4); compared with TBC, *p < 0.05; compared with TBC&BMP-2, #p < 0.05
Fig. 2
Fig. 2
A Four weeks after the operation, the histology of each group was observed (HE staining, ×200); B Quantitative area of new bone formation (n = 3); compared with TBC&Sr, *p < 0.05; compared with TBC&BMP-2, #p < 0.05
Fig. 3
Fig. 3
Rabbit femoral condyle bone repair experiment. A The appearance of experimental material; B The repaired bone 6 weeks after the surgery; C Hard tissue section (HE staining, 40×); D Paraffin section (HE staining, 100×); E Paraffin section (TB staining, 100×); F Quantitative results of the histological sections (n = 3); compared with TBC&Sr, *p < 0.05; compared with TBC&BMP-2, #p < 0.05

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