Synthesis and cytocompatibility of manganese (II) and iron (III) substituted hydroxyapatite nanoparticles
Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Li, Yan [verfasserIn] |
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| Format: |
Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2011 |
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| Schlagwörter: |
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| Anmerkung: |
© Springer Science+Business Media, LLC 2011 |
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| Übergeordnetes Werk: |
Enthalten in: Journal of materials science - Springer US, 1966, 47(2011), 2 vom: 23. Aug., Seite 754-763 |
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| Übergeordnetes Werk: |
volume:47 ; year:2011 ; number:2 ; day:23 ; month:08 ; pages:754-763 |
| Links: |
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| DOI / URN: |
10.1007/s10853-011-5851-7 |
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| Katalog-ID: |
OLC2046372786 |
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| 520 | |a Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. | ||
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| 650 | 4 | |a Field Emission Scanning Electron Microscope Image | |
| 700 | 1 | |a Widodo, Jasmine |4 aut | |
| 700 | 1 | |a Lim, Sierin |4 aut | |
| 700 | 1 | |a Ooi, Chui Ping |4 aut | |
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10.1007/s10853-011-5851-7 doi (DE-627)OLC2046372786 (DE-He213)s10853-011-5851-7-p DE-627 ger DE-627 rakwb eng 670 VZ Li, Yan verfasserin aut Synthesis and cytocompatibility of manganese (II) and iron (III) substituted hydroxyapatite nanoparticles 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. Field Emission Scanning Electron Microscope Simulated Body Fluid Inductively Couple Plasma Osteoblast Cell Field Emission Scanning Electron Microscope Image Widodo, Jasmine aut Lim, Sierin aut Ooi, Chui Ping aut Enthalten in Journal of materials science Springer US, 1966 47(2011), 2 vom: 23. Aug., Seite 754-763 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:47 year:2011 number:2 day:23 month:08 pages:754-763 https://doi.org/10.1007/s10853-011-5851-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_20 GBV_ILN_21 GBV_ILN_23 GBV_ILN_30 GBV_ILN_32 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_4046 GBV_ILN_4305 GBV_ILN_4323 AR 47 2011 2 23 08 754-763 |
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10.1007/s10853-011-5851-7 doi (DE-627)OLC2046372786 (DE-He213)s10853-011-5851-7-p DE-627 ger DE-627 rakwb eng 670 VZ Li, Yan verfasserin aut Synthesis and cytocompatibility of manganese (II) and iron (III) substituted hydroxyapatite nanoparticles 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. Field Emission Scanning Electron Microscope Simulated Body Fluid Inductively Couple Plasma Osteoblast Cell Field Emission Scanning Electron Microscope Image Widodo, Jasmine aut Lim, Sierin aut Ooi, Chui Ping aut Enthalten in Journal of materials science Springer US, 1966 47(2011), 2 vom: 23. Aug., Seite 754-763 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:47 year:2011 number:2 day:23 month:08 pages:754-763 https://doi.org/10.1007/s10853-011-5851-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_20 GBV_ILN_21 GBV_ILN_23 GBV_ILN_30 GBV_ILN_32 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_4046 GBV_ILN_4305 GBV_ILN_4323 AR 47 2011 2 23 08 754-763 |
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10.1007/s10853-011-5851-7 doi (DE-627)OLC2046372786 (DE-He213)s10853-011-5851-7-p DE-627 ger DE-627 rakwb eng 670 VZ Li, Yan verfasserin aut Synthesis and cytocompatibility of manganese (II) and iron (III) substituted hydroxyapatite nanoparticles 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. Field Emission Scanning Electron Microscope Simulated Body Fluid Inductively Couple Plasma Osteoblast Cell Field Emission Scanning Electron Microscope Image Widodo, Jasmine aut Lim, Sierin aut Ooi, Chui Ping aut Enthalten in Journal of materials science Springer US, 1966 47(2011), 2 vom: 23. Aug., Seite 754-763 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:47 year:2011 number:2 day:23 month:08 pages:754-763 https://doi.org/10.1007/s10853-011-5851-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_20 GBV_ILN_21 GBV_ILN_23 GBV_ILN_30 GBV_ILN_32 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_4046 GBV_ILN_4305 GBV_ILN_4323 AR 47 2011 2 23 08 754-763 |
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10.1007/s10853-011-5851-7 doi (DE-627)OLC2046372786 (DE-He213)s10853-011-5851-7-p DE-627 ger DE-627 rakwb eng 670 VZ Li, Yan verfasserin aut Synthesis and cytocompatibility of manganese (II) and iron (III) substituted hydroxyapatite nanoparticles 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. Field Emission Scanning Electron Microscope Simulated Body Fluid Inductively Couple Plasma Osteoblast Cell Field Emission Scanning Electron Microscope Image Widodo, Jasmine aut Lim, Sierin aut Ooi, Chui Ping aut Enthalten in Journal of materials science Springer US, 1966 47(2011), 2 vom: 23. Aug., Seite 754-763 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:47 year:2011 number:2 day:23 month:08 pages:754-763 https://doi.org/10.1007/s10853-011-5851-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_20 GBV_ILN_21 GBV_ILN_23 GBV_ILN_30 GBV_ILN_32 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_4046 GBV_ILN_4305 GBV_ILN_4323 AR 47 2011 2 23 08 754-763 |
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10.1007/s10853-011-5851-7 doi (DE-627)OLC2046372786 (DE-He213)s10853-011-5851-7-p DE-627 ger DE-627 rakwb eng 670 VZ Li, Yan verfasserin aut Synthesis and cytocompatibility of manganese (II) and iron (III) substituted hydroxyapatite nanoparticles 2011 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer Science+Business Media, LLC 2011 Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. Field Emission Scanning Electron Microscope Simulated Body Fluid Inductively Couple Plasma Osteoblast Cell Field Emission Scanning Electron Microscope Image Widodo, Jasmine aut Lim, Sierin aut Ooi, Chui Ping aut Enthalten in Journal of materials science Springer US, 1966 47(2011), 2 vom: 23. Aug., Seite 754-763 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:47 year:2011 number:2 day:23 month:08 pages:754-763 https://doi.org/10.1007/s10853-011-5851-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_20 GBV_ILN_21 GBV_ILN_23 GBV_ILN_30 GBV_ILN_32 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_4046 GBV_ILN_4305 GBV_ILN_4323 AR 47 2011 2 23 08 754-763 |
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All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. 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synthesis and cytocompatibility of manganese (ii) and iron (iii) substituted hydroxyapatite nanoparticles |
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Synthesis and cytocompatibility of manganese (II) and iron (III) substituted hydroxyapatite nanoparticles |
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Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. © Springer Science+Business Media, LLC 2011 |
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Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. © Springer Science+Business Media, LLC 2011 |
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Abstract Manganese (II) and iron (III) substituted hydroxyapatite (HA, $ Ca_{10} $($ PO_{4} $)6(OH)2) nanoparticles were synthesized using wet chemical method. All samples were single-phase, non-stoichiometric and B-type carbonated hydroxyapatite. Compared with pure HA, $ Mn^{2+} $ substituted (MnHA) and $ Fe^{3+} $ doped HA (FeHA) did not demonstrate significant structure deviation. Since ion exchange mechanism was applied for the synthesis process, the morphology and particle size were not significantly affected: all samples were elongated spheroids of around 70 nm. The presence of Fe and Mn was confirmed by energy dispersive X-ray spectroscopy (EDX) while the concentrations were quantified by inductively coupled plasma (ICP). $ Fe^{3+} $ ions were more active than $ Mn^{2+} $ ions in replacing $ Ca^{2+} $ ions in HA lattice structure. The magnetic property of HA was modified by substitution with Fe. The Fe5 ($ Fe_{added} $/$ Ca_{added} $ = 5% by molar ratio) was paramagnetic while pure HA was diamagnetic. Results of extraction assay from cells cultured in extracted medium for 72 h suggested that both MnHA and FeHA were non-cytotoxic to osteoblast cells. Meanwhile, the presence of $ Fe^{3+} $ ions in HA demonstrated significant positive effect on osteoblast cells, where the cell number on Fe5 pellets was twice that of pure HA and MnHA samples. © Springer Science+Business Media, LLC 2011 |
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