scholarly journals Dehydrothermally Cross-Linked Collagen Membrane with a Bone Graft Improves Bone Regeneration in a Rat Calvarial Defect Model

Materials ◽  
2017 ◽  
Vol 10 (8) ◽  
pp. 927 ◽  
Author(s):  
Yin-Zhe An ◽  
Young-Ku Heo ◽  
Jung-Seok Lee ◽  
Ui-Won Jung ◽  
Seong-Ho Choi
Keyword(s):  
Bone Graft ◽  
Bone Regeneration ◽  
Collagen Membrane ◽  
Calvarial Defect ◽  
Defect Model ◽  
Rat Calvarial Defect

Melatonin decorated 3D-printed beta-tricalcium phosphate scaffolds promoting bone regeneration in a rat calvarial defect model

2019 ◽  
Vol 7 (20) ◽  
pp. 3250-3259 ◽  
Author(s):  
Yali Miao ◽  
Yunhua Chen ◽  
Xiao Liu ◽  
Jingjing Diao ◽  
Naru Zhao ◽  
...  
Keyword(s):  
Bone Regeneration ◽  
Tricalcium Phosphate ◽  
Calvarial Defect ◽  
Defect Model ◽  
Beta Tricalcium Phosphate ◽  
3D Printed ◽  
Rat Calvarial Defect

3D-printed β-TCP scaffolds decorated with melatonin via dopamine mussel-inspired chemistry enhance the osteogenesis and in vivo bone regeneration.

Osteogenic Evaluation of Collagen Membrane Containing Drug-Loaded Polymeric Microparticles in a Rat Calvarial Defect Model

2014 ◽  
Vol 20 (23-24) ◽  
pp. 3322-3331 ◽  
Author(s):  
Zheng-Gang Piao ◽  
Jae-Sung Kim ◽  
Jun-Sik Son ◽  
Sook-Young Lee ◽  
Xian-Hao Fang ◽  
...  
Keyword(s):  
Collagen Membrane ◽  
Calvarial Defect ◽  
Defect Model ◽  
Polymeric Microparticles ◽  
Rat Calvarial Defect

Porous 3D Printed Scaffolds For Guided Bone Regeneration In a Rat Calvarial Defect Model

2020 ◽  
Vol 20 ◽  
pp. 100706 ◽  
Author(s):  
Hoang Phuc Dang ◽  
Cedryck Vaquette ◽  
Tara Shabab ◽  
Román A. Pérez ◽  
Ying Yang ◽  
...  
Keyword(s):  
Bone Regeneration ◽  
Guided Bone Regeneration ◽  
Calvarial Defect ◽  
Defect Model ◽  
3D Printed ◽  
Rat Calvarial Defect

scholarly journals Combination of the RANKL-binding peptide W9 and bFGF induces bone regeneration in the rat calvarial defect model

2017 ◽  
Vol 4 (3) ◽  
Author(s):  
Toru Takemoto ◽  
Yuji Kabasawa ◽  
Yusuke Higuchi ◽  
Yasuhiko Tabata ◽  
Kazuhiro Aoki ◽  
...  
Keyword(s):  
Bone Regeneration ◽  
Calvarial Defect ◽  
Defect Model ◽  
Binding Peptide ◽  
Rat Calvarial Defect

Effect of bioactive borate glass microstructure on bone regeneration, angiogenesis, and hydroxyapatite conversion in a rat calvarial defect model

2013 ◽  
Vol 9 (8) ◽  
pp. 8015-8026 ◽  
Author(s):  
Lianxiang Bi ◽  
Mohamed N. Rahaman ◽  
Delbert E. Day ◽  
Zackary Brown ◽  
Christopher Samujh ◽  
...  
Keyword(s):  
Bone Regeneration ◽  
Borate Glass ◽  
Calvarial Defect ◽  
Defect Model ◽  
Rat Calvarial Defect

Evaluation of biocompatibility of α-1,3 galactosyltransferase knockout pig bone graft in a rat calvarial defect model

2014 ◽  
Vol 15 (2) ◽  
pp. 86-91
Author(s):  
Se Eun Kim ◽  
Ga Hoi Choi ◽  
Kyung Mi Shim ◽  
Seok Hwa Choi ◽  
Sang-Myeong Lee ◽  
...  
Keyword(s):  
Bone Graft ◽  
Calvarial Defect ◽  
Defect Model ◽  
Rat Calvarial Defect

scholarly journals Sustained Delivery of Lactoferrin Using Poloxamer Gels for Local Bone Regeneration in a Rat Calvarial Defect Model

Materials ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 212
Author(s):  
Young Eun Park ◽  
Kaushik Chandramouli ◽  
Maureen Watson ◽  
Mark Zhu ◽  
Karen E. Callon ◽  
...  
Keyword(s):  
Immune Response ◽  
Bone Regeneration ◽  
Bone Defect ◽  
Local Delivery ◽  
Burst Release ◽  
Sustained Delivery ◽  
Calvarial Defect ◽  
Defect Model ◽  
Local Bone ◽  
Rat Calvarial Defect

Lactoferrin (LF) is a multifunctional milk glycoprotein that promotes bone regeneration. Local delivery of LF at the bone defect site is a promising approach for enhancement of bone regeneration, but efficient systems for sustained local delivery are still largely missing. The aim of this study was to investigate the potential of the poloxamers for sustained delivery of LF to enhance local bone regeneration. The developed LF/poloxamer formulations were liquid at room temperature (20 °C) transforming to a sustained releasing gel depot at body temperature (37 °C). In vitro release studies demonstrated an initial burst release (~50%), followed by slower release of LF for up to 72 h. Poloxamer, with and without LF, increased osteoblast viability at 72 h (p < 0.05) compared to control, and the immune response from THP-1 cells was mild when compared to the suture material. In rat calvarial defects, the LF/poloxamer group had lower bone volume than the controls (p = 0.0435). No difference was observed in tissue mineral density and lower bone defect coverage scores (p = 0.0267) at 12 weeks after surgery. In conclusion, LF/poloxamer formulations support cell viability and do not induce an unfavourable immune response; however, LF delivery via the current formulation of LF200/poloxamer gel did not demonstrate enhanced bone regeneration and was not compatible with the rat calvarial defect model.

scholarly journals Cathelicidin LL37 Promotes Osteogenic Differentiation in vitro and Bone Regeneration in vivo

2021 ◽  
Vol 9 ◽  
Author(s):  
Lunhao Li ◽  
Yiyu Peng ◽  
Qingyue Yuan ◽  
Jing Sun ◽  
Ai Zhuang ◽  
...  
Keyword(s):  
Bone Regeneration ◽  
Osteogenic Differentiation ◽  
Antibacterial Properties ◽  
Bone Defects ◽  
Optimum Concentration ◽  
Calvarial Defect ◽  
Defect Model ◽  
Calvarial Bone ◽  
Rat Calvarial Defect

Different types of biomaterials have been used to repair the defect of bony orbit. However, exposure and infections are still critical risks in clinical application. Biomaterials with characteristics of osteogenesis and antibiosis are needed for bone regeneration. In this study, we aimed to characterize the antimicrobial effects of cathelicidin-LL37 and to assess any impacts on osteogenic activity. Furthermore, we attempted to demonstrate the feasibility of LL37 as a potential strategy in the reconstruction of clinical bone defects. Human adipose-derived mesenchyme stem cells (hADSCs) were cultured with different concentrations of LL37 and the optimum concentration for osteogenesis was selected for further in vitro studies. We then evaluated the antibiotic properties of LL37 at the optimum osteogenic concentration. Finally, we estimated the efficiency of a PSeD/hADSCs/LL37 combined scaffold on reconstructing bone defects in the rat calvarial defect model. The osteogenic ability on hADSCs in vitro was shown to be dependent on the concentration of LL37 and reached a peak at 4 μg/ml. The optimum concentration of LL37 showed good antimicrobial properties against Escherichia coli and Staphylococcus anurans. The combination scaffold of PSeD/hADSCs/LL37 showed superior osteogenic properties compared to the PSeD/hADSCs, PSeD, and control groups scaffolds, indicating a strong bone reconstruction effect in the rat calvarial bone defect model. In Conclusion, LL37 was shown to promote osteogenic differentiation in vitro as well as antibacterial properties. The combination of PSeD/hADSCs/LL37 was advantageous in the rat calvarial defect reconstruction model, showing high potential in clinical bone regeneration.

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