1.Experimental study in vitro on toxicology and cytocompatibility of collagen/hydroxylapatite (CHA) composite material as part of tracheal prosthesis.
Hongcan SHI ; Zhifei XU ; Xiong QIN ; Xuewei ZHAO ; Kang SUN ; Xiangyang GAO
Journal of Biomedical Engineering 2003;20(4):608-611
Cytotoxicity and cytocompatibility remains the principal theme for biomaterials application in medicine. The purpose of this study was to investigate the cytotoxicity and cytocompatibility of collagen/hydroxyapatite(CHA) composite material in vitro in order to provide useful scientific basis for clinical use. Cellular cultivation in vitro and MTT assay were conducted for evaluating the composite material's influence on the morphology, growth and proliferation of cultured cell(L-929 cell). The hemolysis test was also performed for evaluating the impact on the function and metabolism of erythrocyte. These results demonstrated that the CHA composite material had no cytotoxicity and no hemolytic effect, and it might not be harmful to the morphology of the L-929 cell. The growth and proliferation of the L-929 cell could not be inhibited significantly. The cytotoxicity score of the composite material was grade 0. The hemolysis rate was 1.85%. In conclusion, collagen/hydroxyapatite (CHA) composite material might have good cytocompatibility and be safe for clinical use.
Animals
;
Biocompatible Materials
;
toxicity
;
Cells, Cultured
;
Collagen
;
toxicity
;
Hydroxyapatites
;
toxicity
;
Mice
;
Prostheses and Implants
;
Toxicity Tests
;
Trachea
2.Mutagenicity of CORAGRAF and REKAGRAF in the Ames test.
Suzina AH ; Azlina A ; Shamsuria O ; Samsudin AR
The Medical Journal of Malaysia 2004;59 Suppl B():105-106
Mutagenicity of CORAGRAF (natural coral) and REKAGRAF (hydroxyapatite) was tested in Ames test with and without an external metabolic activation system (S9). The test revealed no mutagenic activity of both locally produced osseous substitutes.
Base Pair Mismatch/drug effects
;
Biotransformation/physiology
;
Bone Substitutes/*toxicity
;
Calcium Carbonate/*toxicity
;
Chromosome Aberrations
;
Escherichia coli/genetics
;
Hydroxyapatites/*toxicity
;
*Materials Testing
;
*Mutagenicity Tests
;
Salmonella typhimurium/genetics
3.Chromosome aberration test for hydroxyapatite in sheep.
Kannan TP ; Nik Ahmad Shah NL ; Azlina A ; Samsudin AR ; Narazah MY ; Salleh M
The Medical Journal of Malaysia 2004;59 Suppl B():168-169
The present study is aimed at finding the mutagenicity and cytotoxicity of dense form of synthetic hydroxyapatite (Source: School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia) in the blood of sheep. The biomaterial was implanted in the tibia of Malin, an indigenous sheep breed of Malaysia. Blood was collected from the sheep before implantation of the biomaterial, cultured and a karyological study was made. Six weeks after implantation, blood was collected from the same animal, cultured and screened for chromosome aberrations. The mitotic indices and karyological analysis indicated that the implantation of synthetic hydroxyapatite (dense form) did not produce any cytotoxicity or chromosome aberrations in the blood of sheep.
Biocompatible Materials/*toxicity
;
Bone Substitutes/*toxicity
;
Bone and Bones/pathology
;
Cell Survival/drug effects
;
*Chromosome Aberrations
;
Hydroxyapatites/*toxicity
;
Karyotyping
;
*Mutagenicity Tests
;
*Prostheses and Implants
;
Sheep
4.DNA damage evaluation of hydroxyapatite on fibroblast cell L929 using the single cell gel electrophoresis assay.
Rajab NF ; Yaakob TA ; Ong BY ; Hamid M ; Ali AM ; Annuar BO ; Inayat-Hussain SH
The Medical Journal of Malaysia 2004;59 Suppl B():170-171
Hydroxyapatite is the main component of the bone which is a potential biomaterial substance that can be applied in orthopaedics. In this study, the biocompatibility of this biomaterial was assessed using an in vitro technique. The cytotoxicity and genotoxicity effect of HA2 and HA3 against L929 fibroblast cell was evaluated using the MTT Assay and Alkaline Comet Assay respectively. Both HA2 and HA3 compound showed low cytotoxicity effect as determined using MTT Assay. Cells viability following 72 hours incubation at maximum concentration of both HA2 and HA3 (200 mg/ml) were 75.3 +/- 8.8% and 86.7 +/- 13.1% respectively. However, the cytotoxicity effect of ZnSO4.7H2O as a positive control showed an IC50 values of 46 mg/ml (160 microM). On the other hand, both HA2 and HA3 compound showed a slight genotoxicity effect as determined using the Alkaline Comet Assay following incubation at the concentration 200 mg/ml for 72 hours. This assay has been widely used in genetic toxicology to detect DNA strand breaks and alkali-labile site. The percentage of the cells with DNA damage for both substance was 27.7 +/- 1.3% and 15.6 +/- 1.0% for HA2 and HA3 respectively. Incubation of the cells for 24 hours with 38 microg/ml (IC25) of positive control showed an increase in percentage of cells with DNA damage (67.5 +/- 0.7%). In conclusion, our study indicated that both hydroxyapatite compounds showed a good biocompatibility in fibroblast cells.
Biocompatible Materials/*toxicity
;
Bone Substitutes/*toxicity
;
Cell Survival/drug effects
;
*DNA Damage
;
Hydroxyapatites/*toxicity
;
L Cells (Cell Line)
;
*Mutagenicity Tests
;
*Prostheses and Implants