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العنوان
Evaluation of Cell proliferation of an Experimentally Fabricated Polymer Scaffold with and without Punica granatum for Bone Regeneration :
المؤلف
Sadek, Khadiga Mostafa.
هيئة الاعداد
باحث / خديجة مصطفى صادق
مشرف / احمد نور الدين احمد حبيب
مشرف / شيماء ابراهيم حبيب
مشرف / وائل ممدوح
الموضوع
Cell proliferation, Bone Regeneration. Punica granatum.
تاريخ النشر
2020
عدد الصفحات
xxii, 193, [1] p. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
Dentistry (miscellaneous)
تاريخ الإجازة
1/1/2020
مكان الإجازة
جامعة القاهرة - الفم والأسنان - Dental Materials
الفهرس
Only 14 pages are availabe for public view

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from 218

Abstract

Aim of the study: Fabrication, characterization, and biological evaluation of a novel polycaprolactone (PCL) nano-scaffold incorporating pomegranate peel extract (PG) for bone regeneration. Methodology: PCL and PG solutions were prepared, and nanofibrous scaffolds were obtained by electrospinning. Three groups of scaffolds were prepared; the control group PCL and the other two groups contained PCL with different PG concentrations (11% and 18%). Fiber morphology, diameter, and distribution were studied using Scanning Electron Microscope (SEM) while the chemical structure was analyzed using Fourier Infrared Spectroscopy (FTIR). Antioxidant activity and total phenolic content (TPC) were studied using 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) test and Folin-Ciocalteu test, respectively. PG release was monitored by spectrophotometer, while porosity measurement was carried out by Brunauer, Emmett and Teller method (BET) and mercury intrusion porosimeter. Degradation analysis was performed up to 21 days. Osteoblastic proliferation and cell attachment on the scaffold’s surface were detected using 3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) and SEM, respectively. Statistical analyses were done using Tukey’s post-Hoc test one-way ANOVA. Results: Scaffold’s characterization showed uniform nanofibers, without beads or fibers entanglement. The fiber diameter ranged between 149 nm and 168 nm while the antioxidant activity and the total phenolic content of the groups containing PG had a significantly higher result compared with the control group. The highest release of PG was detected within the first 48 hours. The porosity of the scaffolds showed an accepted pore diameter size and distribution for bone regeneration. While the degradation of the scaffolds was improved due to the addition of the extract to the polymer. Finally, the cell culture indicated proper osteoblasts proliferation and attachment on the newly fabricated scaffolds containing PG. Conclusion: The incorporation of a natural food waste PG in the PCL nanofibers gave PCL-PG scaffolds with better porosity, pore size diameter distribution, and degradation than the control PCL scaffolds. Furthermore, a significant improvement in osteoblasts attachment and proliferation were detected on the newly fabricated PG scaffolds compared to the negative control group. Such findings may encourage its application in bone regeneration.