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  4. Osteogenic Evaluation of Glutaraldehyde Crosslinked Gelatin Composite with Fetal Rat Calvarial Culture Model
 
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Osteogenic Evaluation of Glutaraldehyde Crosslinked Gelatin Composite with Fetal Rat Calvarial Culture Model

Resource
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS v.25 n.8 pp.644-654
Journal
The International Journal of Artificial Organs
Journal Volume
v.25
Journal Issue
n.8
Pages
644-654
Date Issued
2001
Date
2001
Author(s)
Liu, Hwa-Chang
Yao, Chun-Hsu
Sun, Jui-Sheng
Lee, Chun-Jean
Huang, Chin-Wang
Lin, Feng-Huei  
URI
http://ntur.lib.ntu.edu.tw//handle/246246/128047
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034839098&doi=10.1046%2fj.1525-1594.2001.025008644.x&partnerID=40&md5=6b1d1de1cb4408dc0cf77531f151fdb9
Abstract
The cytotoxicity of the synthetic bone substitute composed of tricalcium phosphate and glutaraldehyde crosslinked gelatin (GTG) were evaluated by osteoblast cell culture. In a previous study, the GTG composites were soaked in distilled water for 1, 2, 4, 7, 14, 28, and 42 days, and then the solutions (or extracts) were cocultured with osteoblasts to evaluate the cytotoxicity of GTG composites by alive cell counting. In this study, the extracts were cocultured with the osteoblasts; thereafter, the concentration of transforming growth factor-beta (TGF-beta1) and prostaglandin E2 (PGE2) in the medium was analyzed to strictly reflect the biological effects of GTG composites on the growth of osteoblasts. In order to investigate the osteoconductive potential of the GTG composites on new bone formation in a relative short term, a model of neonatal rat calvarial organ culture was designed prior to animal experiments. Three experimental materials of 4, 8, and 12% GTG composites were evaluated by fetal rat calvarial organ culture for their ability for bone regeneration. Deproteinized bovine and porcine cancellous bone matrixes were used as the controlled materials. All the organ culture units were maintained in cultured medium for 5 weeks. Following the culture period, the morphology of tissue was observed under an optical microscope, and the quantitative evaluation of the new generation bone was determined by using a semiautomatic histomorphometeric method. Except in the initial 4 days, the concentration of TGF-beta1 of 4% and 8% GTG composites was higher than that of the blank group for all the other experimental time periods. The PGE2 concentration for 4% and 8% GTG composites was lower than that of the blank group. It revealed that the 4% and 8% GTG composites would not lead to inflammation and would promote osteoblast growth. The morphology and activity of the osteoblasts were not transformed or changed by the 2 GTG composites. For the 12% GTG composite, the performance of the in vitro condition was inferior to the blank group and the other 2 GTG composites. Although the concentration of TGF-beta1 and PGE2 was gradually back to normal after 14 days, the morphology of the osteoblasts was abnormal with features such as contracted cytoplast structures. The osteoblast was damaged perhaps in the initial stage. We suggested that the 4% and 8% GTG composites should be soaked in distilled water at least for 4 days before medical applications. The 12% GTG composite and the composites with a concentration of glutaraldehyde solution higher than 12% were not recommended as a medical prostheses in any condition. The fetal rat calvaria culture also showed the same results with the analysis of TGF-beta1 and PGE2. From the study, we could predict the results of animal experiments in the future.
Subjects
Bioabsorbed bone graft
Glutaraldehyde
Tricalcium phospha Tricalcium phosphate
Gelatin
Osteoblast Rat calvarial tissue culture
Other Subjects
Bone; Cytotoxicity; Morphology; Osteoblasts; Tissue culture; Tissue engineering; Bioabsorbed bone graft; Bone graft; Fetal rats; Gelatin; Gelatin composites; Glutaraldehyde crosslinked gelatins; Glutaraldehydes; Organ culture; Rat calvarial tissue culture; Tri-calcium phosphates; Rats; gelatin; glutaraldehyde; prostaglandin E2; transforming growth factor beta1; water; animal cell; animal tissue; article; bone graft; calvaria; cancellous bone; cell count; cell culture; cell growth; chemical composition; composite graft; concentration (parameters); conductance; controlled study; cross linking; culture medium; cytotoxicity; in vitro study; inflammation; microscopy; morphometrics; newborn; nonhuman; osteoblast; priority journal; rat; Animalia; Bovinae; Suidae
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