Polina Sinitsyna
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Polina Sinitsyna has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- Leena Hupa
Laboratory of Molecular Science and Engineering, Åbo Akademi, Henriksgatan 2, 20500 Åbo, Finland
3 shared publications Leena Hupa
2 shared publications- Markus Engblom
Åbo Akademi University, Faculty of Science and Engineering, Turku, Finland
2 shared publications - Adrian Stiller
Laboratory of Molecular Science and Engineering, Åbo Akademi, Henriksgatan 2, 20500 Åbo, Finland
1 shared publication - Bo Jonson
Department of Built Environment and Energy Technology, Linnaeus University, 35195 Växjö, Sweden
1 shared publication - Laura Aalto-Setälä
Johan Gadolin Process Chemistry Centre, Åbo Akademi University, Turku, Finland
1 shared publication
Latest Publications
- Open Access
- 24 September 2026
- Published by Elsevier in Journal of Non-Crystalline Solids
- Vol. 692
Effect of constant and alternating fluid flow conditions on the dissolution of bioactive glass S53P4
- 24 September 2026
- Published by Elsevier in Journal of Non-Crystalline Solids
- Vol. 692
Open AccessEffect of constant and alternating fluid flow conditions on the dissolution of bioactive glass S53P4
- Open Access
- 28 May 2024
- Published by Elsevier in Journal of Non-Crystalline Solids
- Vol. 637
Analysis and modelling of in vitro bioactivity for bioactive glass microspheres and granules in continuous fluid flow conditions
- 28 May 2024
- Published by Elsevier in Journal of Non-Crystalline Solids
- Vol. 637
Open AccessAnalysis and modelling of in vitro bioactivity for bioactive glass microspheres and granules in continuous fluid flow conditions
- Open Access
- 22 August 2023
- Published by Elsevier in Open Ceramics
- Vol. 16
Impact of substituting K2O for Na2O on physico-chemical properties and in vitro bioactivity of bioactive glass S53P4
- 22 August 2023
- Published by Elsevier in Open Ceramics
- Vol. 16
Open AccessImpact of substituting K2O for Na2O on physico-chemical properties and in vitro bioactivity of bioactive glass S53P4
- Open Access
In Vitro Dissolution of Na-Ca-P-Oxynitrides
Sodium-calcium-phosphate based oxynitride glasses and glass-ceramics doped with Mg, Si, and Nb were studied in vitro in simulated body fluid (SBF) under static conditions. The release of ions and pH changes up to 7 days of immersion were investigated. The nitrogen incorporation into phosphate glass matrix was found to notably influence in vitro dissolution only of homogenous glasses. Increasing the nitrogen content in the samples decreased the mean mass loss, while the niobate incorporation increased it. The correlation between the nitrogen content and increase in pH of SBF was also observed. The presence of phosphates crystallites was found to support the dissolution process at the beginning step (up to 3 days).
Open AccessIn Vitro Dissolution of Na-Ca-P-Oxynitrides
Sodium-calcium-phosphate based oxynitride glasses and glass-ceramics doped with Mg, Si, and Nb were studied in vitro in simulated body fluid (SBF) under static conditions. The release of ions and pH changes up to 7 days of immersion were investigated. The nitrogen incorporation into phosphate glass matrix was found to notably influence in vitro dissolution only of homogenous glasses. Increasing the nitrogen content in the samples decreased the mean mass loss, while the niobate incorporation increased it. The correlation between the nitrogen content and increase in pH of SBF was also observed. The presence of phosphates crystallites was found to support the dissolution process at the beginning step (up to 3 days).
- Open Access
Dissolution of Amorphous S53P4 Glass Scaffolds in Dynamic In Vitro Conditions
The silicate-based bioactive glass S53P4 is clinically used in bone regenerative applications in granule form. However, utilization of the glass in scaffold form has been limited by the high tendency of the glass to crystallize during sintering. Here, careful optimization of sintering parameters enabled the manufacture of porous amorphous S53P4 scaffolds with a strength high enough for surgical procedures in bone applications (5 MPa). Sintering was conducted in a laboratory furnace for times ranging from 25 to 300 min at 630 °C, i.e., narrowly below the commencement of the crystallization. The phase composition of the scaffolds was verified with XRD, and the ion release was tested in vitro and compared with granules in continuous flow of Tris buffer and simulated body fluid (SBF). The amorphous, porous S53P4 scaffolds present the possibility of using the glass composition in a wider range of applications.
Open AccessDissolution of Amorphous S53P4 Glass Scaffolds in Dynamic In Vitro Conditions
The silicate-based bioactive glass S53P4 is clinically used in bone regenerative applications in granule form. However, utilization of the glass in scaffold form has been limited by the high tendency of the glass to crystallize during sintering. Here, careful optimization of sintering parameters enabled the manufacture of porous amorphous S53P4 scaffolds with a strength high enough for surgical procedures in bone applications (5 MPa). Sintering was conducted in a laboratory furnace for times ranging from 25 to 300 min at 630 °C, i.e., narrowly below the commencement of the crystallization. The phase composition of the scaffolds was verified with XRD, and the ion release was tested in vitro and compared with granules in continuous flow of Tris buffer and simulated body fluid (SBF). The amorphous, porous S53P4 scaffolds present the possibility of using the glass composition in a wider range of applications.