Porous carbonated hydroxyapatite-based scaffold using simple gas foaming method
Source abstract
Abstract
In this work, snail shells were used as a calcium source in the synthesis of carbonated hydroxyapatite (CHAp) particles using a co-precipitation method. Then, the CHAp was further processed to produce a porous structure scaffold using a simple gas foaming method with H2O2 solution (30%) as a foaming agent, followed by densification at high temperature. Ratio of liquid H2O2 solution/CHAp solid was varied from 0.75/1, 1/1, and 1.25/1 ml/g. A scanning electron microscope (SEM) was used to observe the morphology of samples. Chemical structure and compositions were analyzed by a Fourier transform infrared (FTIR) and an energy dispersive X-ray (EDX). Crystallographic and phase identity of samples were evaluated using an X-ray diffractometer (XRD). XRD, FTIR and EDX results showed the CHAp successfully produced from snail shells. SEM analysis on CHAp morphology indicated that CHAp has a sphere-like grain with a size under 1 μm. Higher ratio of liquid H2O2 solution/CHAp solid brings bigger and richer macro-pores structure in the scaffold, yet microporosity seems to independent to this parameter. High-temperature treatment to densify the scaffold has no profound effect on purity of the final scaffold.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Bone Tissue Engineering Materials · Calcium Carbonate Crystallization and Inhibition · Collagen: Extraction and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics, Faculty of Mathematics and Nature Science, Universitas Gadjah Mada, Yogyakarta, Indonesia
Funding
Kementerian Riset Teknologi Dan Pendidikan Tinggi Republik Indonesia · Rekognisi Tugas Akhir (RTA) UGM · Indonesian Endowment Fund for Education
References (22)
Show source-provided references
1. 10.1007/s10853-013-7864-x10.1007/s10853-013-7864-x ↗
2. 10.1088/1757-899X/432/1/01204410.1088/1757-899X/432/1/012044 ↗
3. 10.1088/1757-899X/546/4/04200110.1088/1757-899X/546/4/042001 ↗
4. 10.1016/j.msec.2007.03.00110.1016/j.msec.2007.03.001 ↗
5. 10.1007/978-3-319-12460-510.1007/978-3-319-12460-5 ↗
6. 10.1007/978-3-319-12460-5_810.1007/978-3-319-12460-5_8 ↗
7. 10.1007/s10856-005-4424-110.1007/s10856-005-4424-1 ↗
8. 10.1021/acsbiomaterials.5b0050910.1021/acsbiomaterials.5b00509 ↗
9. 10.1016/j.msec.2019.11034710.1016/j.msec.2019.110347 ↗
10. 10.5772/intechopen.7019410.5772/intechopen.70194 ↗
11. 10.1016/j.biomaterials.2003.10.06610.1016/j.biomaterials.2003.10.066 ↗
12. 10.4248/BR20130300210.4248/BR201303002 ↗
13. 10.1007/s10853-009-4026-210.1007/s10853-009-4026-2 ↗
14. 10.1088/1757-899X/546/4/04201510.1088/1757-899X/546/4/042015 ↗
15. 10.1016/S0955-2219(03)00304-210.1016/S0955-2219(03)00304-2 ↗
16. 10.1016/j.ceramint.2010.07.01610.1016/j.ceramint.2010.07.016 ↗
17. 10.1007/s41779-019-00334-610.1007/s41779-019-00334-6 ↗
18. 10.1039/c4ce00119b10.1039/c4ce00119b ↗
19. 10.1016/j.ceramint.2018.04.12810.1016/j.ceramint.2018.04.128 ↗
20. 10.1061/(ASCE)0899-1561(2009)21:11(694)10.1061/(ASCE)0899-1561(2009)21:11(694) ↗
21. 10.1080/21870764.2019.159592710.1080/21870764.2019.1595927 ↗
22. 10.1023/A:100862102055510.1023/A:1008621020555 ↗