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العنوان
Preparation And characterization Of Pulp Derived Extracellular Matrix Scaffold For Regenerative Endodontic Applications (An In Vitro Study) /
المؤلف
Thabet, Abdelrahman Mohamed Hossam Eldin Mostafa Hassan.
هيئة الاعداد
باحث / عبدالرحمن محمد حسام الدين مصطفى حسن ثاب ت
مشرف / عمرو محمد عبدالله
مشرف / احمد مصطفى مبارك
مناقش / سيبال مختار موسى
تاريخ النشر
2024.
عدد الصفحات
105p+2. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
طب الأسنان
تاريخ الإجازة
4/7/2024
مكان الإجازة
جامعة الاسكندريه - كلية طب الاسنان - Department of Conservative dentistry
الفهرس
Only 14 pages are availabe for public view

from 104

from 104

Abstract

The use of biological scaffolds in regenerative endodontics has gained much attention in recent years. The development of a new biomimetic scaffold that contains tissue-specific cell homing factors could lead to more predictable tissue regeneration.
Aim of the study: Preparation and characterization of decellularized bovine pulp-derived Extracellular Matrix hydrogel (P-ECM) and pulp-derived extracellular matrix hydrogel/ hyaluronic acid combination (P-ECM + HA) for regenerative endodontic procedures.
Materials and Methods: Freshly extracted bovine molar teeth were collected. Bovine dental pulp tissues were harvested, and stored at -40º C. For decellularization, a 5-day protocol was implemented incorporating trypsin/EDTA, deionized water and DNase treatment. Decellularization was evaluated by DNA quantification and histological examination to assess collagen and Glycosaminoglycans (GAGs) content. This was followed by the preparation of a bovine pulp-derived extracellular matrix hydrogel (P-ECM) and combined with hyaluronic acid (P-ECM + HA). The fabricated scaffolds were then characterized using protein quantification, hydrogel topology and porosity, biodegradability, and growth factor content using Enzyme-linked immunosorbent assay (ELISA) to assess angiogenic and osteogenic growth factors: TGF-β1(Transforming growth factor beta 1), bFGF (bovine basic fibroblast growth factor) and BMP2 (Bone Morphogenetic Protein 2).
Results: Decellularization was histologically confirmed, and DNA content was quantified and was below (50 ng/mg tissue). P-ECM hydrogels were successfully prepared to have a final concentration of 3.00 mg/ml. Total protein content was found to be (439.0 ±123.4 μg/μl) in the prepared hydrogel. P-ECM+HA showed sustained protein release while the P-ECM group showed gradual decreasing release. Degradation was higher in P-ECM+HA and it had a significantly larger fiber diameter, While P-ECM had a larger pore area percentage. ELISA confirmed the retention and release of growth factors where P-ECM hydrogel had higher BMP2 release, while P-ECM+HA had higher release of TGF-β1 and bFGF.
Conclusion: Both P-ECM and P-ECM+HA retained their bioactive properties demonstrating a potential role as functionalized scaffolds for regenerative endodontic procedures.
Keywords: Biomimetics, Biological Scaffolds, Cell Homing, Extracellular Matrix, Hydrogels, Regenerative Endodontics, Tissue Engineering