Figures & data
Figure 1 SEM (A) and TEM (B) micrographs of nDPB, EDS (C) of nDPB, and N2 adsorption–desorption isotherms (D) of nDPB (pore size distribution insert in D).
Note: The magnification of (A) is 6.00K, the magnification of (B) is 300.00K.
Abbreviations: EDS, energy-dispersive spectrometry; nDPB, nanoporous diopside bioglass; SEM, scanning electron microscopy; TEM, transmission electron microscopy.
![Figure 1 SEM (A) and TEM (B) micrographs of nDPB, EDS (C) of nDPB, and N2 adsorption–desorption isotherms (D) of nDPB (pore size distribution insert in D).Note: The magnification of (A) is 6.00K, the magnification of (B) is 300.00K.Abbreviations: EDS, energy-dispersive spectrometry; nDPB, nanoporous diopside bioglass; SEM, scanning electron microscopy; TEM, transmission electron microscopy.](/cms/asset/fcc872b4-7e2f-4dab-bd28-a0828659ad82/dijn_a_12194047_f0001_b.jpg)
Figure 2 SEM micrographs of surface morphology of GL (A, B), 15nDGC (C, D) and 30nDGC (E, F) scaffolds; EDS mapping of GL (G), 15nDGC (H) and 30nDGC (I), and yellow dots represent Si element, indicating the distribution of nDPB particles into GL.
Note: The magnification of (A, C and E) is ×50, the magnification of (B, D and F) is ×200, the magnification of (G, H and I) is ×10,000.
Abbreviations: EDS, energy-dispersive spectrometry; GL, gliadin; nDPB, nanoporous diopside bioglass; SEM, scanning electron microscopy; 15nDGC, DGC scaffolds with 15 wt% nDPB; 30nDGC, DGC scaffolds with 30 wt% nDPB.
![Figure 2 SEM micrographs of surface morphology of GL (A, B), 15nDGC (C, D) and 30nDGC (E, F) scaffolds; EDS mapping of GL (G), 15nDGC (H) and 30nDGC (I), and yellow dots represent Si element, indicating the distribution of nDPB particles into GL.Note: The magnification of (A, C and E) is ×50, the magnification of (B, D and F) is ×200, the magnification of (G, H and I) is ×10,000.Abbreviations: EDS, energy-dispersive spectrometry; GL, gliadin; nDPB, nanoporous diopside bioglass; SEM, scanning electron microscopy; 15nDGC, DGC scaffolds with 15 wt% nDPB; 30nDGC, DGC scaffolds with 30 wt% nDPB.](/cms/asset/bd2ab70e-f54e-4f63-965b-f1dae76f77b2/dijn_a_12194047_f0002_b.jpg)
Figure 3 FTIR spectra (A) of nDPB, GL, 15nDGC and 30nDGC scaffolds; weight loss (B) of the scaffolds after being immersed in PBS solution for different time periods; pH changes (C) of solution after soaking the scaffolds in PBS for different time periods; changes of Ca, Mg, Si ion concentrations (D) in solution after soaking 30nDGC scaffolds in PBS for different time periods.
Abbreviations: FTIR, Fourier transform infrared; GL, gliadin; nDPB, nanoporous diopside bioglass; PBS, phosphate-buffered saline.
![Figure 3 FTIR spectra (A) of nDPB, GL, 15nDGC and 30nDGC scaffolds; weight loss (B) of the scaffolds after being immersed in PBS solution for different time periods; pH changes (C) of solution after soaking the scaffolds in PBS for different time periods; changes of Ca, Mg, Si ion concentrations (D) in solution after soaking 30nDGC scaffolds in PBS for different time periods.Abbreviations: FTIR, Fourier transform infrared; GL, gliadin; nDPB, nanoporous diopside bioglass; PBS, phosphate-buffered saline.](/cms/asset/2964129a-1f7f-4cb6-9082-96c724285cc2/dijn_a_12194047_f0003_c.jpg)
Figure 4 Cell attachment ratio (A) of the MC3T3-E1 cells on the scaffolds for 6, 12 and 24 h (*p<0.05), SEM images of cells: GL (B), 15nDGC (C) and 30nDGC (D) scaffolds for 12 h.
Note: The magnification of (B, C and D) is ×250.
Abbreviations: GL, gliadin; SEM, scanning electron microscopy.
![Figure 4 Cell attachment ratio (A) of the MC3T3-E1 cells on the scaffolds for 6, 12 and 24 h (*p<0.05), SEM images of cells: GL (B), 15nDGC (C) and 30nDGC (D) scaffolds for 12 h.Note: The magnification of (B, C and D) is ×250.Abbreviations: GL, gliadin; SEM, scanning electron microscopy.](/cms/asset/45019156-1859-4f69-8a95-572d55656c17/dijn_a_12194047_f0004_c.jpg)
Figure 5 OD values of the MC3T3-E1 cells on GL, 15nDGC and 30nDGC scaffolds for 1, 4 and 7 days, *p<0.05.
Abbreviations: GL, gliadin; OD, optical density.
![Figure 5 OD values of the MC3T3-E1 cells on GL, 15nDGC and 30nDGC scaffolds for 1, 4 and 7 days, *p<0.05.Abbreviations: GL, gliadin; OD, optical density.](/cms/asset/31a662da-8291-48e9-908e-75b61f681c2e/dijn_a_12194047_f0005_c.jpg)
Figure 6 CLSM images of morphology of MC3T3-E1 cells after being cultured on GL, 15nDGC and 30nDGC scaffolds for 4 days.
Abbreviations: CLSM, confocal laser scanning microscopy; DAPI, 4′,6′-diamidino-2-phenylindole; FITC, fluorescein isothiocyanate; GL, gliadin.
![Figure 6 CLSM images of morphology of MC3T3-E1 cells after being cultured on GL, 15nDGC and 30nDGC scaffolds for 4 days.Abbreviations: CLSM, confocal laser scanning microscopy; DAPI, 4′,6′-diamidino-2-phenylindole; FITC, fluorescein isothiocyanate; GL, gliadin.](/cms/asset/2998ecad-c046-4395-9bf1-a77f5c17f68f/dijn_a_12194047_f0006_c.jpg)
Figure 7 H&E staining of histological sections of GL (A), 15nDGC (B) and 30nDGC (C) scaffolds implanted into femoral defects for 1, 2 and 3 months.
Abbreviations: GL, gliadin; H&E, hematoxylin and eosin.
![Figure 7 H&E staining of histological sections of GL (A), 15nDGC (B) and 30nDGC (C) scaffolds implanted into femoral defects for 1, 2 and 3 months.Abbreviations: GL, gliadin; H&E, hematoxylin and eosin.](/cms/asset/73f70f96-8340-43b6-824c-797328df93d1/dijn_a_12194047_f0007_c.jpg)
Figure 8 Percentage of new bone area (A) and material residual (B) after GL, 15nDGC and 30nDGC scaffolds were implanted into femoral defects of rabbits for 1, 2 and 3 months, *p<0.05.
Abbreviation: GL, gliadin.
![Figure 8 Percentage of new bone area (A) and material residual (B) after GL, 15nDGC and 30nDGC scaffolds were implanted into femoral defects of rabbits for 1, 2 and 3 months, *p<0.05.Abbreviation: GL, gliadin.](/cms/asset/ea7bc3ad-5adc-43f9-a484-d3c1592f77ba/dijn_a_12194047_f0008_c.jpg)