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Article: A novel, doped calcium silicate bioceramic synthesized by sol–gel method: Investigation of setting time and biological properties
Title | A novel, doped calcium silicate bioceramic synthesized by sol–gel method: Investigation of setting time and biological properties |
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Authors | |
Keywords | calcium silicate sol–gel zinc magnesium setting time |
Issue Date | 2020 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.interscience.wiley.com/jpages/0021-9304:1/ |
Citation | Journal of Biomedical Materials Research Part B: Applied Biomaterials, 2020, v. 108 n. 1, p. 56-66 How to Cite? |
Abstract | The aim of the current study was to synthesize a fast‐setting ion‐doped calcium silicate bioceramic by the sol–gel method and to characterize its in vitro apatite‐forming ability and cell viability. Calcium silicate (CS), doped calcium silicate with zinc and magnesium, with Ca/Zn molar ratios of 6.7:1 (DCS1), and 4.5:1 (DCS2), were synthesized by the sol–gel method. Matreva white MTA (WMTA, Matreva, CA, Egypt) was used as a control. The synthesized powders were characterized by x‐ray diffraction. Setting time was measured using the Gilmore needle indentation technique. The in vitro apatite‐forming ability of the materials was evaluated by scanning electron microscope and energy dispersive X‐ray. NIH3T3‐E1 cells viability was tested using MTT assay. The ion release of Ca, Si, Zn, and Mg was measured using inductive coupled plasma‐optical emission spectroscopy (ICP‐OES). One‐way ANOVA was used to analyze setting time results. The Tukey's HSD post hoc test was used to establish significance (p < 0.001). For nonparametric data, the Kruskal–Wallis H test with Dunn's correction for post hoc comparison was used (p < 0.05). CS, DCS1, and DCS2 showed a significant decrease in setting time 33 ± 1.63 min, 28 ± 1.63 min, and 41.75 ± 2.87 min, respectively, compared to WMTA 91 ± 3.16 min (p < 0.001). DCS1 showed the highest apatite‐forming ability and cell viability compared to the other groups. Ca and Si ions release decreased in both DCS1 and DCS2. The physical and biological properties of CS can be successfully improved by the sol–gel synthesis and ions doping. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 108B:56–66, 2020. |
Persistent Identifier | http://hdl.handle.net/10722/281784 |
ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 0.634 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Abdalla, MM | - |
dc.contributor.author | Lung, CYK | - |
dc.contributor.author | Neelakantan, P | - |
dc.contributor.author | Matinlinna, JP | - |
dc.date.accessioned | 2020-03-27T04:22:29Z | - |
dc.date.available | 2020-03-27T04:22:29Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Journal of Biomedical Materials Research Part B: Applied Biomaterials, 2020, v. 108 n. 1, p. 56-66 | - |
dc.identifier.issn | 1552-4973 | - |
dc.identifier.uri | http://hdl.handle.net/10722/281784 | - |
dc.description.abstract | The aim of the current study was to synthesize a fast‐setting ion‐doped calcium silicate bioceramic by the sol–gel method and to characterize its in vitro apatite‐forming ability and cell viability. Calcium silicate (CS), doped calcium silicate with zinc and magnesium, with Ca/Zn molar ratios of 6.7:1 (DCS1), and 4.5:1 (DCS2), were synthesized by the sol–gel method. Matreva white MTA (WMTA, Matreva, CA, Egypt) was used as a control. The synthesized powders were characterized by x‐ray diffraction. Setting time was measured using the Gilmore needle indentation technique. The in vitro apatite‐forming ability of the materials was evaluated by scanning electron microscope and energy dispersive X‐ray. NIH3T3‐E1 cells viability was tested using MTT assay. The ion release of Ca, Si, Zn, and Mg was measured using inductive coupled plasma‐optical emission spectroscopy (ICP‐OES). One‐way ANOVA was used to analyze setting time results. The Tukey's HSD post hoc test was used to establish significance (p < 0.001). For nonparametric data, the Kruskal–Wallis H test with Dunn's correction for post hoc comparison was used (p < 0.05). CS, DCS1, and DCS2 showed a significant decrease in setting time 33 ± 1.63 min, 28 ± 1.63 min, and 41.75 ± 2.87 min, respectively, compared to WMTA 91 ± 3.16 min (p < 0.001). DCS1 showed the highest apatite‐forming ability and cell viability compared to the other groups. Ca and Si ions release decreased in both DCS1 and DCS2. The physical and biological properties of CS can be successfully improved by the sol–gel synthesis and ions doping. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 108B:56–66, 2020. | - |
dc.language | eng | - |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.interscience.wiley.com/jpages/0021-9304:1/ | - |
dc.relation.ispartof | Journal of Biomedical Materials Research Part B: Applied Biomaterials | - |
dc.rights | Preprint This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Postprint This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | - |
dc.subject | calcium silicate | - |
dc.subject | sol–gel | - |
dc.subject | zinc magnesium | - |
dc.subject | setting time | - |
dc.title | A novel, doped calcium silicate bioceramic synthesized by sol–gel method: Investigation of setting time and biological properties | - |
dc.type | Article | - |
dc.identifier.email | Neelakantan, P: prasanna@hku.hk | - |
dc.identifier.email | Matinlinna, JP: jpmat@hku.hk | - |
dc.identifier.authority | Neelakantan, P=rp02214 | - |
dc.identifier.authority | Matinlinna, JP=rp00052 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/jbm.b.34365 | - |
dc.identifier.pmid | 30920144 | - |
dc.identifier.scopus | eid_2-s2.0-85063564867 | - |
dc.identifier.hkuros | 309502 | - |
dc.identifier.hkuros | 315951 | - |
dc.identifier.volume | 108 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | 56 | - |
dc.identifier.epage | 66 | - |
dc.identifier.isi | WOS:000500822700007 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1552-4973 | - |