Possible Proliferative Impact of Human Platelet-Rich Fibrin Obtained From Controlled Type 2 Diabetic Patients on Human Dental Pulp Stem Cells (In Vitro Study)
Amer, M., Elhindawy, M., Zaher, A. (2643). Possible Proliferative Impact of Human Platelet-Rich Fibrin Obtained From Controlled Type 2 Diabetic Patients on Human Dental Pulp Stem Cells (In Vitro Study). EKB Journal Management System, 2022(3), -. doi: 10.21608/adjg.2022.73553.1355
Mona Amer; Menatalla Elhindawy; Ahmed Zaher. "Possible Proliferative Impact of Human Platelet-Rich Fibrin Obtained From Controlled Type 2 Diabetic Patients on Human Dental Pulp Stem Cells (In Vitro Study)". EKB Journal Management System, 2022, 3, 2643, -. doi: 10.21608/adjg.2022.73553.1355
Amer, M., Elhindawy, M., Zaher, A. (2643). 'Possible Proliferative Impact of Human Platelet-Rich Fibrin Obtained From Controlled Type 2 Diabetic Patients on Human Dental Pulp Stem Cells (In Vitro Study)', EKB Journal Management System, 2022(3), pp. -. doi: 10.21608/adjg.2022.73553.1355
Amer, M., Elhindawy, M., Zaher, A. Possible Proliferative Impact of Human Platelet-Rich Fibrin Obtained From Controlled Type 2 Diabetic Patients on Human Dental Pulp Stem Cells (In Vitro Study). EKB Journal Management System, 2643; 2022(3): -. doi: 10.21608/adjg.2022.73553.1355

Possible Proliferative Impact of Human Platelet-Rich Fibrin Obtained From Controlled Type 2 Diabetic Patients on Human Dental Pulp Stem Cells (In Vitro Study)

Al-Azhar Journal of Dentistry
Volume 2022, Issue 3, July 2022  XML
DOI: 10.21608/adjg.2022.73553.1355
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Authors
Mona Amer1; Menatalla Elhindawy2; Ahmed Zaher3
1Demonstrator at Faculty of Dentistry, Horus University.
2Lecturer of Oral Biology, Faculty of Dentistry, Mansoura University.
3Professor of Oral Biology, Faculty of Dentistry, Mansoura University.
Abstract
Purpose: This study was carried out in order to assess the effect of 10% PRF exudate obtained from controlled type 2 diabetic patients on proliferation capacity of dental pulp stem cells (DPSCs). Then 1% PRF exudate obtained from controlled type 2 diabetic patients was tested for osteogenic capability after 1 week. Material and methods: PRF exudates were prepared using the direct method from 8 healthy donors (control group) and 8 controlled type 2 diabetic patients (study group). In 96-well plates, DPSCs harvested from pulp tissue of impacted lower third molar were treated with 10% PRF exudate obtained from healthy donors and controlled type 2 diabetic patients for 1,3 and 5 days. The effects of exudates on proliferation and cell viability were tested using the MTS assay. For osteogenic capability, DPSCs were treated with 1%PRF exudate obtained from healthy donors and controlled type 2 diabetic patients supplemented with osteogenic medium for 1week and the osteodifferentiation assay was held using alizarin red stain with ELIZA reader. All data were subjected into one-way Anova statistical analysis. Results: The concentrations of 10% and 1% PRF exudates obtained from controlled type 2 diabetic patients had proliferative and osteoinductive effects on DPSCs comparable to that of the healthy individuals. Conclusion: Based on our study, controlled type 2 diabetic patients can be treated similar to their Unaffected peers using 10% PRF exudates as the optimal concentration for DPSCs proliferation and 1% PRF exudates as the optimal concentration for DPSCs osteodifferentiation and formation of mineralized nodules in 7 days.
Keywords
Diabetes mellitus; PRF; DPSCs
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