Calcium phosphate formation from sea urchin - (brissus latecarinatus) via modified mechano-chemical (ultrasonic) conversion method

This study aims to produce apatite structures, such as hydroxyapatite (HA) and fluorapatite (FA), from precursor calcium phosphates of biological origin, namely from sea urchin, with mechano-chemical stirring and hot-plating conversion method. The produced materials were heat treated at 800 °C for 4 hours. X-ray diffraction and scanning electron microscopy (SEM) studies were conducted. Calcium phosphate phases were developed. The SEM images showed the formation of micro to nano-powders. The experimental results suggest that sea urchin, Brissus latecarinatus skeleton could be an alternative source for the production of various mono or biphasic calcium phosphates with simple and economic mechano-chemical (ultrasonic) conversion method

Sintering effects of mullite-doping on mechanical properties of bovine hydroxyapatite

In this study, sintering effects on microstructural behavior of bovine derived hydroxyapatite doped with powder mullite are considered in the temperature range between 1000 °C and 1300 °C. Results show that maximum values of both compressive strength and microhardness are achieved in the samples sintered at 1200 °C for all mullite additions of 5, 7.5, 10 and 12.5 wt%. Moreover, above 1000 °C, decomposition of HA and new phase formations such as whitlockite and gehlenite play a major role in both compressive strength and microhardness properties which increase up to 10 wt% mullite reinforcement. © 2017 Elsevier B.V

Part 2: biocompatibility evaluation of hydroxyapatite-based clinoptilolite and Al2O3 composites

The biocompatibility of clinoptilolite/alumina/bovine hydroxyapatite (Cp - Al2O3 - BHA) composite, at different ratio obtained by powder pressing process, were investigated studying the behavior of osteosarcoma (SAOS-2) cells. The biocompatibility was examined by means of cytotoxicity and cytocompatibility tests. The structure and morphology of bioceramic composites were studied by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) technique. The results showed that these materials have no toxic effects. The natural composite that fabricated in this study may be a promising approach for bone engineering applications

Synthesis and cytotoxicity analysis of porous β-TCP/starch bioceramics

The production of porous ceramics for biomedical applications is widely available in the Ceramics industry. In bioceramic applications, interconnected pores are pertinent to increase osteoconductivity and cell proliferation. However, an increase in pore size and the pore amount decrease the mechanical properties. For this reason, pore properties must be precisely controlled. In this study, the effect of a natural pore-forming agent, corn starch addition, and sintering conditions on mechanical properties and biocompatibility was investigated. During mixing, four different starch amounts (1, 3, 5, and 10 wt%) were added to pure beta-tricalcium phosphate (β-TCP) ceramic powders and pressed. Pressed pellets were sintered at 1000, 1100, 1200, and 1300 °C. A scanning electron microscope (SEM) is used to investigate microstructure, texture, pore size, and cell adhesion. The mechanical properties of the β-TCP ceramic parts were further characterized by measuring the density and compressive strength. Cytotoxicity tests were carried out with MTT assays. The optimum mechanical properties were obtained at 1100 °C sintered biocomposites. Although starch starts to burn around 410 °C and analytical results show no presence of starch after the sintering process, biocomposites initially containing 10% starch showed improved cell proliferation. However, a reduction of 59% in compressive strength and a 16% reduction in the density were also recorded. It was observed that 10 wt% starch addition increases cell proliferation by 10% in sintered β-TCP samples. Starch powder additions can be used to increase the cell viability of the material by facilitating the creation of pores, as a low-cost pore-forming agent for porous bone graft and non-load-bearing material in both orthopaedics and maxillofacial applications. Graphical abstract: [Figure not available: see fulltext.

Sintering effects of mullite-doping on mechanical properties of bovine hydroxyapatite

In this study, sintering effects on microstructural behavior of bovine derived hydroxyapatite doped with powder mullite are considered in the temperature range between 1000 C-omicron and 1300 C-omicron. Results show that maximum values of both compressive strength and microhardness are achieved in the samples sintered at 1200 C-omicron for all mullite additions of 5, 7.5, 10 and 12.5 wt. Moreover, above 1000 C-omicron, decomposition of HA and new phase formations such as whitlockite and gehlenite play a major role in both compressive strength and microhardness properties which increase up to 10 wt mullite reinforcement. (C) 2017 Elsevier B.V. All rights reserved

Preparation and evaluation of cerium oxide-bovine hydroxyapatite composites for biomedical engineering applications

The fabrication and characterization of bovine hydroxyapatite (BHA) and cerium oxide (CeO2) composites are presented. CeO2 (at varying concentrations 1, 5 and 10wt%) were added to calcinated BHA powder. The resulting mixtures were shaped into green cylindrical samples by powder pressing (350MPa) followed by sintering in air (1000-1300°C for 4h). Density, Vickers microhardness (HV), compression strength, scanning electron microscopy (SEM) and X-ray diffraction (XRD) studies were performed on the products. The sintering behavior, microstructural characteristics and mechanical properties were evaluated. Differences in the sintering temperature (for 1wt% CeO2 composites) between 1200 and 1300°C, show a 3.3% increase in the microhardness (564 and 582.75HV, respectively). Composites prepared at 1300°C demonstrate the greatest compression strength with comparable results for 5 and 10wt% CeO2 content (106 and 107MPa) which are significantly better than those for 1wt% and those that do not include any CeO2 (90 and below 60MPa, respectively). The results obtained suggest optimal parameters to be used in preparation of BHA and CeO2 composites, while also highlighting the potential of such materials in several biomedical engineering applications. © 2014 Elsevier Ltd.2003K120810This study was carried out mainly with the equipment furnished (between 2007–2008) to Marmara University with the support of the Turkish Republic Government Planning Organization in the framework of the project 2003K120810 “Manufacturing and Characterization of Electro-Conductive Bioceramics”