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. 2019 Mar 22;10(1):16. doi: 10.3390/jfb10010016

Table 2.

In vivo studies of composites comprising β-TCP for guided bone regeneration.

Material Fabrication Model/Defect Time Points Results Ref.
rhBMP-2/PCL/PLGA/β-TCP 3D printing Calvaria, rabbit 8 weeks Bone turn over significantly higher than control group (p < 0.05).
Bone to implant contact ratio significantly higher (p < 0.05).
Full or partial absorption of implant observed.
[111]
PCL/PLGA/β-TCP/rhBMP-2 3D printing Lower Jaw, Beagle Dog 4 to 8 weeks The stability of the membrane was maintained at 4 weeks (post-implantation).
Complete healing; new bone deposition observed.
Significant increase in bone formation from 4 to 8 weeks.
No inflammatory reaction.
[109]
PCL/PLGA/β-TCP 3D printing Extracted premolars; mandibular alveolar ridge; Beagle Dog 8 weeks Higher levels of new bone area and bone implant contact, compared to the control (collagen membrane).
Remaining biomaterial was much higher compared to control.
Results were insignificant to each other.
[112]
Modified Silk/β-TCP Casting, particle deposition Rabbit; Calvaria 5 and 10 weeks Control (collagen membrane)
Rate of resorption higher in control compared to membrane.
Silk/β-TCP highly support bone formation and restoration of microarchitecture of defect compared to the control.
Less statistical difference from histomorphometric data between the two (p < 0.05).
[113]
β-TCP/HA granules N/A Minipig; Lower premolar 3 and 8 weeks Group with higher percentage of β-TCP (90%) showed more mineralized bone. [114]
Gelatin/β-TCP Freeze-dried/Cross-linking Calvaria, Rat 2, 4, 8 weeks Bone volume was higher in Gelatin/β-TCP membrane compared to control.
Absorption was greater in collagen compared to Gelatin/β-TCP.
No significant difference in bone volume between collagen
membrane and Gelatin/β-TCP.
[115]
Bio-Oss/β-TCP/rhPDGF N/A Calvaria; Rat 2, 4, 6, 8, 10 weeks Significant increase in bone mineral density.
A 30% reduction in mean volume of remnant bone particles.
[116]

2 PCL (polycaprolactone); rhPDGF (recombinant human platelet-derived growth factor); N/A (no explicit description of the material development process).