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Gold is for the mistress, silver for the maid: Enhanced mechanical properties, osteoinduction and antibacterial activity due to iron doping of tricalcium phosphate bone cements

Self-hardening calcium phosphate cements present ideal bone tissue substitutes from the standpoints of bioactivity and biocompatibility, yet they suffer from (a) weak mechanical properties, (b) negligible osteoinduction without the use of exogenous growth factors, and (c) a lack of intrinsic antibac...

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Published in:Materials Science & Engineering C 2019-01, Vol.94, p.798-810
Main Authors: Uskoković, Vuk, Graziani, Valerio, Wu, Victoria M., Fadeeva, Inna V., Fomin, Alexander S., Presniakov, Igor A., Fosca, Marco, Ortenzi, Marzo, Caminiti, Ruggero, Rau, Julietta V.
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cited_by cdi_FETCH-LOGICAL-c4478-31bb512cc809306f246d172feb1075e511e5582fdf2398fb4b81a4f4e466da053
cites cdi_FETCH-LOGICAL-c4478-31bb512cc809306f246d172feb1075e511e5582fdf2398fb4b81a4f4e466da053
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container_title Materials Science & Engineering C
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creator Uskoković, Vuk
Graziani, Valerio
Wu, Victoria M.
Fadeeva, Inna V.
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Fosca, Marco
Ortenzi, Marzo
Caminiti, Ruggero
Rau, Julietta V.
description Self-hardening calcium phosphate cements present ideal bone tissue substitutes from the standpoints of bioactivity and biocompatibility, yet they suffer from (a) weak mechanical properties, (b) negligible osteoinduction without the use of exogenous growth factors, and (c) a lack of intrinsic antibacterial activity. Here we attempt to improve on these deficiencies by studying the properties of self-setting Fe-doped bone-integrative cements containing two different concentrations of the dopant: 0.49 and 1.09 wt% Fe. The hardening process, which involved the transformation of Fe-doped β-tricalcium phosphate (Fe-TCP) to nanocrystalline brushite, was investigated in situ by continuously monitoring the cements using the Energy Dispersive X-Ray Diffraction technique. The setting time was 20 min and the hardening time 2 h, but it took 50 h for the cement to completely stabilize compositionally and mechanically. Still, compared to other similar systems, the phase transformation during hardening was relatively fast and it also followed a relatively simple reaction path, virtually free of complex intermediates and noisy background. Mössbauer spectrometry demonstrated that 57Fe atoms in Fe-TCP were located in two non-equivalent crystallographic sites and distributed over positions with a strong crystal distortion. The pronounced presence of ultrafine crystals in the final, brushite phase contributed to the reduction of the porosity and thereby to the enhancement of the mechanical properties. The compressive strength of the hardened TCP cements increased by more than twofold when Fe was added as a dopant, i.e., from 11.5 ± 0.5 to 24.5 ± 2.0 MPa. The amount of iron released from the cements in physiological media steadied after 10 days and was by an order of magnitude lower than the clinical threshold that triggers the toxic response. The cements exhibited osteoinductive activity, as observed from the elevated levels of expression of genes encoding for osteocalcin and Runx2 in both undifferentiated and differentiated MC3T3-E1 cells challenged with the cements. The osteoinductive effect was inversely proportional to the content of Fe ions in the cements, indicating that an excessive amount of iron can have a detrimental effect on the induction of bone growth by osteoblasts in contact with the cement. In contrast, the antibacterial activity of the cement in the agar assay increased against all four bacterial species analysed (E. coli, S. enteritidis, P. aeruginosa, S. aur
doi_str_mv 10.1016/j.msec.2018.10.028
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Here we attempt to improve on these deficiencies by studying the properties of self-setting Fe-doped bone-integrative cements containing two different concentrations of the dopant: 0.49 and 1.09 wt% Fe. The hardening process, which involved the transformation of Fe-doped β-tricalcium phosphate (Fe-TCP) to nanocrystalline brushite, was investigated in situ by continuously monitoring the cements using the Energy Dispersive X-Ray Diffraction technique. The setting time was 20 min and the hardening time 2 h, but it took 50 h for the cement to completely stabilize compositionally and mechanically. Still, compared to other similar systems, the phase transformation during hardening was relatively fast and it also followed a relatively simple reaction path, virtually free of complex intermediates and noisy background. Mössbauer spectrometry demonstrated that 57Fe atoms in Fe-TCP were located in two non-equivalent crystallographic sites and distributed over positions with a strong crystal distortion. The pronounced presence of ultrafine crystals in the final, brushite phase contributed to the reduction of the porosity and thereby to the enhancement of the mechanical properties. The compressive strength of the hardened TCP cements increased by more than twofold when Fe was added as a dopant, i.e., from 11.5 ± 0.5 to 24.5 ± 2.0 MPa. The amount of iron released from the cements in physiological media steadied after 10 days and was by an order of magnitude lower than the clinical threshold that triggers the toxic response. The cements exhibited osteoinductive activity, as observed from the elevated levels of expression of genes encoding for osteocalcin and Runx2 in both undifferentiated and differentiated MC3T3-E1 cells challenged with the cements. The osteoinductive effect was inversely proportional to the content of Fe ions in the cements, indicating that an excessive amount of iron can have a detrimental effect on the induction of bone growth by osteoblasts in contact with the cement. In contrast, the antibacterial activity of the cement in the agar assay increased against all four bacterial species analysed (E. coli, S. enteritidis, P. aeruginosa, S. aureus) in direct proportion with the concentration of Fe ions in it, indicating their key effect on the promotion of the antibacterial effect in this material. This effect was less pronounced in broth assays. Experiments involving co-incubation of cements with cells in an alternate magnetic radiofrequency field for 30 min demonstrated a good potential for the use of these magnetic cements in hyperthermia cancer therapies. Specifically, the population of human glioblastoma cells decreased six-fold at the 24 h time point following the end of the magnetic field treatment, while the population of the bone cancer cells dropped approximately twofold. The analysis of the MC3T3-E1 cell/cement interaction reiterated the effects of iron in the cement on the bone growth marker expression by showing signs of adverse effects on the cell morphology and proliferation only for the cement containing the higher concentration of Fe ions (1.09 wt%). Biological testing concluded that the effects of iron are beneficial from the perspective of a magnetic hyperthermia therapy and antibacterial prophylaxis, but its concentration in the material must be carefully optimized to avoid the adverse effects induced above a certain level of iron concentrations. •Self-setting Fe-doped bone cements with two dopant concentrations were prepared.•Cements exhibited osteoinductivity inversely proportional to the Fe ions content.•Cements exhibited antibacterial activity against E. coli, S. enteritidis, P. aeruginosa, S. aureus.•Glioblastoma and bone cancer cell populations declined due to magnetic field treatment.•Effects of Fe are beneficial from the perspective of a magnetic hyperthermia therapy.</description><identifier>ISSN: 0928-4931</identifier><identifier>EISSN: 1873-0191</identifier><identifier>DOI: 10.1016/j.msec.2018.10.028</identifier><identifier>PMID: 30423766</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Air hardening ; Animals ; Anti-Bacterial Agents - pharmacology ; Antibacterial activity ; Antibacterial materials ; Background noise ; Biocompatibility ; Biological activity ; Biomedical materials ; Bone cancer ; Bone cement ; Bone cements ; Bone Cements - pharmacology ; Bone growth ; Calcium ; Calcium phosphates ; Calcium Phosphates - chemistry ; Cancer ; Cbfa-1 protein ; Cell Line ; Cell morphology ; Cement ; Compressive strength ; Core Binding Factor Alpha 1 Subunit - metabolism ; Crystallography ; Crystals ; Cytology ; Dopants ; E coli ; Escherichia coli ; Gene expression ; Genetic transformation ; Glioblastoma ; Glioblastoma cells ; Gold ; Gold - pharmacology ; Growth factors ; Hardening behaviour ; Hardening rate ; Humans ; Hyperthermia ; Intermediates ; Ions ; Iron ; Iron - chemistry ; Iron 57 ; Iron-doped tricalcium phosphate ; Kinetics ; Magnetic fields ; Materials science ; Mechanical properties ; Mice ; Morphology ; Osseointegration - drug effects ; Osteoblastic MC3T3-E1 ; Osteoblasts ; Osteoblasts - cytology ; Osteoblasts - metabolism ; Osteocalcin ; Osteocalcin - genetics ; Osteocalcin - metabolism ; Osteogenesis ; Phase transitions ; Porosity ; Powders ; Prophylaxis ; Pseudomonas aeruginosa ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Salmonella enteritidis ; Side effects ; Silver ; Silver - pharmacology ; Spectrometry ; Spectroscopy, Mossbauer ; Spectrum Analysis, Raman ; Staphylococcus aureus ; Temperature ; X-Ray Diffraction</subject><ispartof>Materials Science &amp; Engineering C, 2019-01, Vol.94, p.798-810</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Jan 1, 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4478-31bb512cc809306f246d172feb1075e511e5582fdf2398fb4b81a4f4e466da053</citedby><cites>FETCH-LOGICAL-c4478-31bb512cc809306f246d172feb1075e511e5582fdf2398fb4b81a4f4e466da053</cites><orcidid>0000-0002-7953-1853</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30423766$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uskoković, Vuk</creatorcontrib><creatorcontrib>Graziani, Valerio</creatorcontrib><creatorcontrib>Wu, Victoria M.</creatorcontrib><creatorcontrib>Fadeeva, Inna V.</creatorcontrib><creatorcontrib>Fomin, Alexander S.</creatorcontrib><creatorcontrib>Presniakov, Igor A.</creatorcontrib><creatorcontrib>Fosca, Marco</creatorcontrib><creatorcontrib>Ortenzi, Marzo</creatorcontrib><creatorcontrib>Caminiti, Ruggero</creatorcontrib><creatorcontrib>Rau, Julietta V.</creatorcontrib><title>Gold is for the mistress, silver for the maid: Enhanced mechanical properties, osteoinduction and antibacterial activity due to iron doping of tricalcium phosphate bone cements</title><title>Materials Science &amp; Engineering C</title><addtitle>Mater Sci Eng C Mater Biol Appl</addtitle><description>Self-hardening calcium phosphate cements present ideal bone tissue substitutes from the standpoints of bioactivity and biocompatibility, yet they suffer from (a) weak mechanical properties, (b) negligible osteoinduction without the use of exogenous growth factors, and (c) a lack of intrinsic antibacterial activity. Here we attempt to improve on these deficiencies by studying the properties of self-setting Fe-doped bone-integrative cements containing two different concentrations of the dopant: 0.49 and 1.09 wt% Fe. The hardening process, which involved the transformation of Fe-doped β-tricalcium phosphate (Fe-TCP) to nanocrystalline brushite, was investigated in situ by continuously monitoring the cements using the Energy Dispersive X-Ray Diffraction technique. The setting time was 20 min and the hardening time 2 h, but it took 50 h for the cement to completely stabilize compositionally and mechanically. Still, compared to other similar systems, the phase transformation during hardening was relatively fast and it also followed a relatively simple reaction path, virtually free of complex intermediates and noisy background. Mössbauer spectrometry demonstrated that 57Fe atoms in Fe-TCP were located in two non-equivalent crystallographic sites and distributed over positions with a strong crystal distortion. The pronounced presence of ultrafine crystals in the final, brushite phase contributed to the reduction of the porosity and thereby to the enhancement of the mechanical properties. The compressive strength of the hardened TCP cements increased by more than twofold when Fe was added as a dopant, i.e., from 11.5 ± 0.5 to 24.5 ± 2.0 MPa. The amount of iron released from the cements in physiological media steadied after 10 days and was by an order of magnitude lower than the clinical threshold that triggers the toxic response. The cements exhibited osteoinductive activity, as observed from the elevated levels of expression of genes encoding for osteocalcin and Runx2 in both undifferentiated and differentiated MC3T3-E1 cells challenged with the cements. The osteoinductive effect was inversely proportional to the content of Fe ions in the cements, indicating that an excessive amount of iron can have a detrimental effect on the induction of bone growth by osteoblasts in contact with the cement. In contrast, the antibacterial activity of the cement in the agar assay increased against all four bacterial species analysed (E. coli, S. enteritidis, P. aeruginosa, S. aureus) in direct proportion with the concentration of Fe ions in it, indicating their key effect on the promotion of the antibacterial effect in this material. This effect was less pronounced in broth assays. Experiments involving co-incubation of cements with cells in an alternate magnetic radiofrequency field for 30 min demonstrated a good potential for the use of these magnetic cements in hyperthermia cancer therapies. Specifically, the population of human glioblastoma cells decreased six-fold at the 24 h time point following the end of the magnetic field treatment, while the population of the bone cancer cells dropped approximately twofold. The analysis of the MC3T3-E1 cell/cement interaction reiterated the effects of iron in the cement on the bone growth marker expression by showing signs of adverse effects on the cell morphology and proliferation only for the cement containing the higher concentration of Fe ions (1.09 wt%). Biological testing concluded that the effects of iron are beneficial from the perspective of a magnetic hyperthermia therapy and antibacterial prophylaxis, but its concentration in the material must be carefully optimized to avoid the adverse effects induced above a certain level of iron concentrations. •Self-setting Fe-doped bone cements with two dopant concentrations were prepared.•Cements exhibited osteoinductivity inversely proportional to the Fe ions content.•Cements exhibited antibacterial activity against E. coli, S. enteritidis, P. aeruginosa, S. aureus.•Glioblastoma and bone cancer cell populations declined due to magnetic field treatment.•Effects of Fe are beneficial from the perspective of a magnetic hyperthermia therapy.</description><subject>Air hardening</subject><subject>Animals</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibacterial activity</subject><subject>Antibacterial materials</subject><subject>Background noise</subject><subject>Biocompatibility</subject><subject>Biological activity</subject><subject>Biomedical materials</subject><subject>Bone cancer</subject><subject>Bone cement</subject><subject>Bone cements</subject><subject>Bone Cements - pharmacology</subject><subject>Bone growth</subject><subject>Calcium</subject><subject>Calcium phosphates</subject><subject>Calcium Phosphates - chemistry</subject><subject>Cancer</subject><subject>Cbfa-1 protein</subject><subject>Cell Line</subject><subject>Cell morphology</subject><subject>Cement</subject><subject>Compressive strength</subject><subject>Core Binding Factor Alpha 1 Subunit - metabolism</subject><subject>Crystallography</subject><subject>Crystals</subject><subject>Cytology</subject><subject>Dopants</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Gene expression</subject><subject>Genetic transformation</subject><subject>Glioblastoma</subject><subject>Glioblastoma cells</subject><subject>Gold</subject><subject>Gold - pharmacology</subject><subject>Growth factors</subject><subject>Hardening behaviour</subject><subject>Hardening rate</subject><subject>Humans</subject><subject>Hyperthermia</subject><subject>Intermediates</subject><subject>Ions</subject><subject>Iron</subject><subject>Iron - 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pharmacology</topic><topic>Growth factors</topic><topic>Hardening behaviour</topic><topic>Hardening rate</topic><topic>Humans</topic><topic>Hyperthermia</topic><topic>Intermediates</topic><topic>Ions</topic><topic>Iron</topic><topic>Iron - chemistry</topic><topic>Iron 57</topic><topic>Iron-doped tricalcium phosphate</topic><topic>Kinetics</topic><topic>Magnetic fields</topic><topic>Materials science</topic><topic>Mechanical properties</topic><topic>Mice</topic><topic>Morphology</topic><topic>Osseointegration - drug effects</topic><topic>Osteoblastic MC3T3-E1</topic><topic>Osteoblasts</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>Osteocalcin</topic><topic>Osteocalcin - genetics</topic><topic>Osteocalcin - metabolism</topic><topic>Osteogenesis</topic><topic>Phase transitions</topic><topic>Porosity</topic><topic>Powders</topic><topic>Prophylaxis</topic><topic>Pseudomonas aeruginosa</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Salmonella enteritidis</topic><topic>Side effects</topic><topic>Silver</topic><topic>Silver - pharmacology</topic><topic>Spectrometry</topic><topic>Spectroscopy, Mossbauer</topic><topic>Spectrum Analysis, Raman</topic><topic>Staphylococcus aureus</topic><topic>Temperature</topic><topic>X-Ray Diffraction</topic><toplevel>online_resources</toplevel><creatorcontrib>Uskoković, Vuk</creatorcontrib><creatorcontrib>Graziani, Valerio</creatorcontrib><creatorcontrib>Wu, Victoria M.</creatorcontrib><creatorcontrib>Fadeeva, Inna V.</creatorcontrib><creatorcontrib>Fomin, Alexander S.</creatorcontrib><creatorcontrib>Presniakov, Igor A.</creatorcontrib><creatorcontrib>Fosca, Marco</creatorcontrib><creatorcontrib>Ortenzi, Marzo</creatorcontrib><creatorcontrib>Caminiti, Ruggero</creatorcontrib><creatorcontrib>Rau, Julietta V.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Materials Science &amp; Engineering C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uskoković, Vuk</au><au>Graziani, Valerio</au><au>Wu, Victoria M.</au><au>Fadeeva, Inna V.</au><au>Fomin, Alexander S.</au><au>Presniakov, Igor A.</au><au>Fosca, Marco</au><au>Ortenzi, Marzo</au><au>Caminiti, Ruggero</au><au>Rau, Julietta V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gold is for the mistress, silver for the maid: Enhanced mechanical properties, osteoinduction and antibacterial activity due to iron doping of tricalcium phosphate bone cements</atitle><jtitle>Materials Science &amp; Engineering C</jtitle><addtitle>Mater Sci Eng C Mater Biol Appl</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>94</volume><spage>798</spage><epage>810</epage><pages>798-810</pages><issn>0928-4931</issn><eissn>1873-0191</eissn><abstract>Self-hardening calcium phosphate cements present ideal bone tissue substitutes from the standpoints of bioactivity and biocompatibility, yet they suffer from (a) weak mechanical properties, (b) negligible osteoinduction without the use of exogenous growth factors, and (c) a lack of intrinsic antibacterial activity. Here we attempt to improve on these deficiencies by studying the properties of self-setting Fe-doped bone-integrative cements containing two different concentrations of the dopant: 0.49 and 1.09 wt% Fe. The hardening process, which involved the transformation of Fe-doped β-tricalcium phosphate (Fe-TCP) to nanocrystalline brushite, was investigated in situ by continuously monitoring the cements using the Energy Dispersive X-Ray Diffraction technique. The setting time was 20 min and the hardening time 2 h, but it took 50 h for the cement to completely stabilize compositionally and mechanically. Still, compared to other similar systems, the phase transformation during hardening was relatively fast and it also followed a relatively simple reaction path, virtually free of complex intermediates and noisy background. Mössbauer spectrometry demonstrated that 57Fe atoms in Fe-TCP were located in two non-equivalent crystallographic sites and distributed over positions with a strong crystal distortion. The pronounced presence of ultrafine crystals in the final, brushite phase contributed to the reduction of the porosity and thereby to the enhancement of the mechanical properties. The compressive strength of the hardened TCP cements increased by more than twofold when Fe was added as a dopant, i.e., from 11.5 ± 0.5 to 24.5 ± 2.0 MPa. The amount of iron released from the cements in physiological media steadied after 10 days and was by an order of magnitude lower than the clinical threshold that triggers the toxic response. The cements exhibited osteoinductive activity, as observed from the elevated levels of expression of genes encoding for osteocalcin and Runx2 in both undifferentiated and differentiated MC3T3-E1 cells challenged with the cements. The osteoinductive effect was inversely proportional to the content of Fe ions in the cements, indicating that an excessive amount of iron can have a detrimental effect on the induction of bone growth by osteoblasts in contact with the cement. In contrast, the antibacterial activity of the cement in the agar assay increased against all four bacterial species analysed (E. coli, S. enteritidis, P. aeruginosa, S. aureus) in direct proportion with the concentration of Fe ions in it, indicating their key effect on the promotion of the antibacterial effect in this material. This effect was less pronounced in broth assays. Experiments involving co-incubation of cements with cells in an alternate magnetic radiofrequency field for 30 min demonstrated a good potential for the use of these magnetic cements in hyperthermia cancer therapies. Specifically, the population of human glioblastoma cells decreased six-fold at the 24 h time point following the end of the magnetic field treatment, while the population of the bone cancer cells dropped approximately twofold. The analysis of the MC3T3-E1 cell/cement interaction reiterated the effects of iron in the cement on the bone growth marker expression by showing signs of adverse effects on the cell morphology and proliferation only for the cement containing the higher concentration of Fe ions (1.09 wt%). Biological testing concluded that the effects of iron are beneficial from the perspective of a magnetic hyperthermia therapy and antibacterial prophylaxis, but its concentration in the material must be carefully optimized to avoid the adverse effects induced above a certain level of iron concentrations. •Self-setting Fe-doped bone cements with two dopant concentrations were prepared.•Cements exhibited osteoinductivity inversely proportional to the Fe ions content.•Cements exhibited antibacterial activity against E. coli, S. enteritidis, P. aeruginosa, S. aureus.•Glioblastoma and bone cancer cell populations declined due to magnetic field treatment.•Effects of Fe are beneficial from the perspective of a magnetic hyperthermia therapy.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30423766</pmid><doi>10.1016/j.msec.2018.10.028</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-7953-1853</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0928-4931
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issn 0928-4931
1873-0191
language eng
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source ScienceDirect Freedom Collection
subjects Air hardening
Animals
Anti-Bacterial Agents - pharmacology
Antibacterial activity
Antibacterial materials
Background noise
Biocompatibility
Biological activity
Biomedical materials
Bone cancer
Bone cement
Bone cements
Bone Cements - pharmacology
Bone growth
Calcium
Calcium phosphates
Calcium Phosphates - chemistry
Cancer
Cbfa-1 protein
Cell Line
Cell morphology
Cement
Compressive strength
Core Binding Factor Alpha 1 Subunit - metabolism
Crystallography
Crystals
Cytology
Dopants
E coli
Escherichia coli
Gene expression
Genetic transformation
Glioblastoma
Glioblastoma cells
Gold
Gold - pharmacology
Growth factors
Hardening behaviour
Hardening rate
Humans
Hyperthermia
Intermediates
Ions
Iron
Iron - chemistry
Iron 57
Iron-doped tricalcium phosphate
Kinetics
Magnetic fields
Materials science
Mechanical properties
Mice
Morphology
Osseointegration - drug effects
Osteoblastic MC3T3-E1
Osteoblasts
Osteoblasts - cytology
Osteoblasts - metabolism
Osteocalcin
Osteocalcin - genetics
Osteocalcin - metabolism
Osteogenesis
Phase transitions
Porosity
Powders
Prophylaxis
Pseudomonas aeruginosa
RNA, Messenger - genetics
RNA, Messenger - metabolism
Salmonella enteritidis
Side effects
Silver
Silver - pharmacology
Spectrometry
Spectroscopy, Mossbauer
Spectrum Analysis, Raman
Staphylococcus aureus
Temperature
X-Ray Diffraction
title Gold is for the mistress, silver for the maid: Enhanced mechanical properties, osteoinduction and antibacterial activity due to iron doping of tricalcium phosphate bone cements
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