Effects of the Sintering Process on Nacre-Derived Hydroxyapatite Scaffolds for Bone Engineering

• Published in: Molecules (Basel, Switzerland) Switzerland), 2020-07, Vol.25 (14), p.3129
• Main Authors: Megat Abdul Wahab, Rohaya, Abdullah, Nurmimie, Zainal Ariffin, Shahrul Hisham, Che Abdullah, Che Azurahanim, Yazid, Farinawati
• Format: Article
• Language: English
• Subjects: Alkaline phosphatase; Animals; Biological activity; Biomaterials; Biomedical materials; Biomolecules; Bone and Bones - cytology; Bone and Bones - metabolism; Bone biomaterials; bone engineering; Bones; Calcium carbonate; Cell differentiation; Cell Line; Cell morphology; Cell viability; Chemical composition; Chemical precipitation; Computed tomography; Crack propagation; Cytology; Defects; Dentistry; Deoxyribonucleic acid; Differentiation; Disease transmission; DNA; Durapatite - chemistry; Electron states; Field emission microscopy; Hydroxyapatite; marine scaffold; Mechanical properties; Mice; Morphology; Nacre; Nacre - chemistry; Osteoblasts - cytology; Osteoblasts - metabolism; Osteocalcin; Particle size; Polymerase chain reaction; Pore size; Scaffolds; Scanning electron microscopy; Sintering; Sintering (powder metallurgy); Skin & tissue grafts; Tissue Engineering; Tissue Scaffolds - chemistry
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules25143129

A hydroxyapatite scaffold is a suitable biomaterial for bone tissue engineering due to its chemical component which mimics native bone. Electronic states which present on the surface of hydroxyapatite have the potential to be used to promote the adsorption or transduction of biomolecules such as protein or DNA. This study aimed to compare the morphology and bioactivity of sinter and nonsinter marine-based hydroxyapatite scaffolds. Field emission scanning electron microscopy (FESEM) and micro-computed tomography (microCT) were used to characterize the morphology of both scaffolds. Scaffolds were co-cultured with 5 × 10 /cm of MC3T3-E1 preosteoblast cells for 7, 14, and 21 days. FESEM was used to observe the cell morphology, and MTT and alkaline phosphatase (ALP) assays were conducted to determine the cell viability and differentiation capacity of cells on both scaffolds. Real-time polymerase chain reaction (rtPCR) was used to identify the expression of osteoblast markers. The sinter scaffold had a porous microstructure with the presence of interconnected pores as compared with the nonsinter scaffold. This sinter scaffold also significantly supported viability and differentiation of the MC3T3-E1 preosteoblast cells ( < 0.05). The marked expression of Col1α1 and osteocalcin (OCN) osteoblast markers were also observed after 14 days of incubation ( < 0.05). The sinter scaffold supported attachment, viability, and differentiation of preosteoblast cells. Hence, sinter hydroxyapatite scaffold from nacreous layer is a promising biomaterial for bone tissue engineering.