The Effect of Calcium Phosphate Ceramic Composition and Structure on In Vitro Precipitation Reactions

2009 ◽  
pp. 140-140-9
Author(s):  
P Ducheyne ◽  
S Radin
Keyword(s):  
Calcium Phosphate ◽  
Calcium Phosphate Ceramic ◽  
Ceramic Composition ◽  
Composition And Structure ◽  
Precipitation Reactions

Gene Expression of C2C12 Cells on Calcium Phosphate Ceramic In Vitro

2005 ◽  
pp. 265-268
Author(s):  
Yan Fei Tan ◽  
Ling Li Zhang ◽  
Xin Lai He ◽  
Wei Qiang Xiao ◽  
Hong Song Fan ◽  
...  
Keyword(s):  
Gene Expression ◽  
Calcium Phosphate ◽  
C2c12 Cells ◽  
Calcium Phosphate Ceramic

scholarly journals Ultrastructural study of degradation of calcium phosphate ceramic by human monocytes and modulation of this activity by HILDA/LIF cytokine.

1996 ◽  
Vol 44 (10) ◽  
pp. 1131-1140 ◽  
Author(s):  
M D Benahmed ◽  
D Heymann ◽  
M Berreur ◽  
M Cottrel ◽  
A Godard ◽  
...  
Keyword(s):  
Calcium Phosphate ◽  
Culture Medium ◽  
Marked Decrease ◽  
Calcium Phosphate Ceramic ◽  
Multinuclear Cells ◽  
Residual Bodies ◽  
First Time

Biodegradation of ceramics in vivo is achieved essentially by monocytes and multinuclear cells (osteoclasts). Monocytes are the key element in this process because they intervene first at the biomaterial implantation site during inflammatory reaction. In this work, in vitro studies were conducted on an ultrastructural scale to determine the specific behavior of these cells with regard to a calcium phosphate (CaP) ceramic. Two types of phagocytosis were observed when cells came into contact with the biomaterial: either CaP crystals were taken up alone and then dissolved in the cytoplasm after disappearance of the phagosome membrane or they were incorporated together with large quantities of culture medium, in which case dissolution occurred after the formation of heterophagosomes. Phagocytosis of CaP coincided with autophagy and the accumulation of residual bodies in the cells. Addition of HILDA/LIF factor to these cultures induced a very marked decrease in phagocytotic activity directed at the capture of CaP crystals and culture medium. Autophagy was reduced, and residual bodies were rare or absent. This study specifies the role of monocytes in CaP biodegradation and demonstrates for the first time that HILDA/LIF has a biological effect on this cell line.

Gene Expression of C2C12 Cells on Calcium Phosphate Ceramic In Vitro

2005 ◽  
Vol 288-289 ◽  
pp. 265-268 ◽  
Author(s):  
Yan Fei Tan ◽  
Ling Li Zhang ◽  
Xin Lai He ◽  
Wei Qiang Xiao ◽  
Hong Song Fan ◽  
...  
Keyword(s):  
Calcium Phosphate ◽  
Type I Collagen ◽  
C2c12 Cell ◽  
C2c12 Cells ◽  
Type I ◽  
Calcium Phosphate Ceramic ◽  
Mtt Method ◽  
Difference Expression

The osteoinduction of Calcium Phosphate (CaP) had been proved and generally been investigated by in vivo implantation. However, the mechanism of the osteoinductivity was not clear and it was difficult to judge the osteoinductivity in vitro. In this study, Mouse C2C12 cell line, a kind of myoblast precursor cell, was employed to co-culture with CaP. The induction of cell differentiation by materials was tested by MTT method, fluorescence observation, especially the mRNA expression of Osteocalcin, Type I collagen and Fibronectin by RT-PCR. It was founded that C2C12 cells could be induced to expression osteocalcin when growth on the surface of the HA/TCP ceramics. At the same time, the ceramics with different composition and sintering temperature seemed to induce difference expression level of the related genes. The results proved that phase composition was one of the most important factors in the regulation of bone-related genes. This study provided a potential model to evaluate the osteoinductivity of CaP ceramics in vitro.

In vitro study of matrix surface properties of porous granulated calcium phosphate ceramic materials made in Russia

2008 ◽  
Vol 145 (4) ◽  
pp. 499-503 ◽  
Author(s):  
V. I. Chissov ◽  
I. K. Sviridova ◽  
N. S. Sergeeva ◽  
V. A. Kirsanova ◽  
S. A. Achmedova ◽  
...  
Keyword(s):  
Calcium Phosphate ◽  
Surface Properties ◽  
In Vitro Study ◽  
Ceramic Materials ◽  
Vitro Study ◽  
Calcium Phosphate Ceramic ◽  
Matrix Surface ◽  
Made In

Calcium Phosphate Precipitation in Liposomal Suspensions

1989 ◽  
Vol 174 ◽  
Author(s):  
Edward D. Eanes
Keyword(s):  
Calcium Phosphate ◽  
Lipid Vesicles ◽  
Matrix Vesicles ◽  
Liposomal Membrane ◽  
Liposomal Membranes ◽  
Precipitation Reactions ◽  
Basic Features ◽  
Calcium Phosphate Precipitation

AbstractArtificial lipid vesicles (liposomes) provide an in vitro approach for microencapsulating calcium phosphate precipitation reactions in a manner similar to that which occurs in matrix vesicles, the initial loci for extracellular mineralization in many skeletal tissues. Apatitic precipitates readily form within the aqueous interiors of liposomes prepared from phosphatidylcholine, dicetylphosphate, and cholesterol when the liposomal membranes enclosing pH 7.4 buffered PO4 solutions are made permeable to external Ca2+ with ionophores. If the external Ca solution is rendered metastable with PO4, the apatitic precipitates rapidly expand to outside the liposomes as well. The present paper describes the basic features of liposomal mineralization and presents some specific examples on how compositional alterations in the liposomal membrane and external Ca solution can affect the progress of this mineralization.

Studies of the solubility of different calcium phosphate ceramic particles in vitro

Biomaterials ◽  
1990 ◽  
Vol 11 (7) ◽  
pp. 509-512 ◽  
Author(s):  
Christel P.A.T. Klein ◽  
J.M.A de Blieck-Hogemrst ◽  
J.G.C. Wolket ◽  
K. de Groot
Keyword(s):  
Calcium Phosphate ◽  
Calcium Phosphate Ceramic ◽  
Ceramic Particles

scholarly journals Icaritin Enhancing Bone Formation Initiated by Sub-Microstructured Calcium Phosphate Ceramic for Critical Size Defect Repair

2020 ◽  
Vol 7 ◽  
Author(s):  
Haitao Peng ◽  
Jianxiao Li ◽  
Yanan Xu ◽  
Guoyu Lv
Keyword(s):  
Calcium Phosphate ◽  
Bone Formation ◽  
Bone Tissue ◽  
Tissue Regeneration ◽  
Bone Defects ◽  
Bone Tissue Regeneration ◽  
Calcium Phosphate Ceramic ◽  
Dose Dependent

Adequate bone tissue regeneration has been challenging to achieve at critical-sized bone defects caused by disease. Bone tissue engineering using a combination of scaffolds and bioactive factors provides new hope for the treatment of this extreme condition. Icaritin, a herb-derived chemical, has shown its ability to enhance bone formation both in vitro and in vivo, and it has been found that sub-micron surface structure instructs bone formation in calcium phosphate ceramics (CaPs). Here, we evaluated the possibility of using a submicron surface structured CaP ceramic as the carrier of icaritin for bone tissue regeneration in critical-sized bone defects. Icaritin, an herb-derived chemical, was loaded into a submicron surface structured porous calcium phosphate ceramic (Ø12.8 × 3 mm) to get samples with 0, 10, 50, 250, and 1,250 µg icaritin per CaP disc (M0, M10, M50, M250, M1250 groups, respectively). In vitro evaluation with the certain dosages correlated to those released from the samples showed a dose-dependent enhancement of osteogenic differentiation and mineralization of human bone marrow stromal cells with the presence of osteogenic factors in the culture medium, indicating icaritin is an osteopromotive factor. After intramuscular implantation of the samples in dogs for 8 weeks, a dose-dependent of bone formation was seen with enhanced bone formation at the dosage of 50 and 250 µg. To evaluate the in vivo osteogenic potentials of icaritin-containing CaP ceramic scaffolds in the orthopedic site, a 12.8 mm calvarial defect model in rabbits was established. Micro-computed tomography (micro-CT) and histology results at weeks 4, 8 and 12 post-surgery showed more newly formed bone in M250 group, with correspondingly more new vessel ingrowth. The results presented herein suggested that being osteopromotive, icaritin could enhance bone formation initiated by sub-microstructured CaP ceramics and the CaP ceramics scaffold incorporating icaritin is a promising biomaterial for the treatment of critical-sized defect.

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