Biological Performance of Dental Biphasic Calcium Phosphate Ceramics Modified by Cold Plasma

2008 ◽  
Vol 368-372 ◽  
pp. 1264-1267 ◽  
Author(s):  
Bao Hui Su ◽  
Jing Chun Su ◽  
Jun Guo Ran ◽  
Bao Yue Su

HA/ß-TCP is one kind of important bone tissue engineering scaffold materials. In order to improve the biological performance of materials, HA/ß-TCP ceramics were modified by the cold plasma technique in this paper. The biological performances of treated materials were evaluated by the results of bone-like apatite formation in SBF, the coculture of the C2C12 cell line and HA/ß-TCP, cell proliferation experiments, observations of the electron microscopy and fluorescence staining and the animal intramuscular implantation experiments. The results showed that after immersion, compared with untreated HA/ß-TCP, treated materials were more conducive to form bone-like apatite; modified HA/ß-TCP could promote the cell proliferation more; the cells grew in the course of nature on the treated scaffold and modified HA/ß-TCP had better bone-forming performance in vivo. It was concluded that modified HA/ß-TCP had better biological performance; the cold plasma technique could improve the biological performance of dental biphasic calcium phosphate ceramics.

Rare Metals ◽  
2021 ◽  
Author(s):  
Chun-Sheng Shao ◽  
Liang-Jian Chen ◽  
Rui-Min Tang ◽  
Bo Zhang ◽  
Jiang-Jie Tang ◽  
...  

RSC Advances ◽  
2018 ◽  
Vol 8 (26) ◽  
pp. 14646-14653 ◽  
Author(s):  
Kun Zhang ◽  
Jieyu Zhang ◽  
Kelei Chen ◽  
Xuefeng Hu ◽  
Yunbing Wang ◽  
...  

Nanostructured porous biphasic calcium phosphate ceramics are able to significantly promote bone defect healing in an osteoporotic environment.


2005 ◽  
Vol 125 (3) ◽  
pp. 153-159 ◽  
Author(s):  
Franck Jegoux ◽  
Eric Goyenvalle ◽  
Maurice Bagot D’arc ◽  
Eric Aguado ◽  
Guy Daculsi

2005 ◽  
Vol 284-286 ◽  
pp. 289-292 ◽  
Author(s):  
Ji Yong Chen ◽  
You Rong Duan ◽  
Xing Dong Zhang

Two sets of porous biphasic calcium phosphate ceramics (BCP) were prepared for dynamic SBF experiment: porous BCP with micropores on the walls of macropores( set A) and porous BCP with dense walls of macropores (set B). Apatite layer could only formed on the macropore walls with micropores. Four groups of specimens were prepared for animal experiments. Group A was porous BCP ceramics with micropores on the walls of macropores; group B was porous BCP with dense walls of macropores; group C was porous BCP ceramics with apatite layers formed by static SBF[2]on their surfaces; group D was porous BCP ceramics with apatite layers formed by dynamic SBF on their walls of macropores. The result of dynamic SBF animal experiments showed that microstructure of BCP played an important role in the bone-like apatite formation and osteoinductiion in biomaterials. Apatite formation may be the prerequisite of osteoinductive formation of new bone.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Meadhbh Á. Brennan ◽  
Mario Barilani ◽  
Francesco Rusconi ◽  
Julien de Lima ◽  
Luciano Vidal ◽  
...  

AbstractBone marrow mesenchymal stem/stromal cells (BMSCs) show great promise for bone repair, however they are isolated by an invasive bone marrow harvest and their regenerative potential decreases with age. Conversely, cord blood can be collected non-invasively after birth and contains MSCs (CBMSCs) that can be stored for future use. However, whether CBMSCs can replace BMSCs targeting bone repair is unknown. This study evaluates the in vitro osteogenic potential of unprimed, osteogenically primed, or chondrogenically primed CBMSCs and BMSCs and their in vivo bone forming capacity following ectopic implantation on biphasic calcium phosphate ceramics in nude mice. In vitro, alkaline phosphatase (intracellular, extracellular, and gene expression), and secretion of osteogenic cytokines (osteoprotegerin and osteocalcin) was significantly higher in BMSCs compared with CBMSCs, while CBMSCs demonstrated superior chondrogenic differentiation and secretion of interleukins IL-6 and IL-8. BMSCs yielded significantly more cell engraftment and ectopic bone formation compared to CBMSCs. However, priming of CBMSCs with either chondrogenic or BMP-4 supplements led to bone formation by CBMSCs. This study is the first direct quantification of the bone forming abilities of BMSCs and CBMSCs in vivo and, while revealing the innate superiority of BMSCs for bone repair, it provides avenues to induce osteogenesis by CBMSCs.


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