Szczegóły publikacji

Opis bibliograficzny

Effect of $Sm^{3+}$ ions on structure and reactivity of S53P4 and 13–93 bioactive glasses / Agata Baranowska, Marcin Kochanowicz, Aleksandra Wajda, Magdalena LEŚNIAK, Piotr Miluski, Dawid Łysik, Piotr JELEŃ, Maciej SITARZ, Zbigniew Olejniczak, Dominik DOROSZ // Spectrochimica Acta . Part A, Molecular and Biomolecular Spectroscopy ; ISSN  1386-1425. — 2026 — vol. 349 art. no. 127299, s. 1-19. — Bibliogr. s. 17-19, Abstr. — Publikacja dostępna online od: 2025-12-03

Autorzy (10)

Słowa kluczowe

bioactivityglass networkSm3+-dopinghydroxyapatite formationion release

Dane bibliometryczne

ID BaDAP166139
Data dodania do BaDAP2026-03-11
Tekst źródłowyURL
DOI10.1016/j.saa.2025.127299
Rok publikacji2026
Typ publikacjiartykuł w czasopiśmie
Otwarty dostęptak
Czasopismo/seriaSpectrochimica Acta, Part A, Molecular and Biomolecular Spectroscopy

Abstract

Bioactive glasses are widely recognized for their ability to bond with living tissues and stimulate regenerative processes, making them a cornerstone in the development of advanced biomaterials. Incorporating rare earth (RE) elements enables the integration of optical functionalities with biological activity while modifying network connectivity. However, previous studies have mainly focused on luminescent performance, and the structural mechanisms by which individual REE dopants influence dissolution kinetics and bioactivity remain insufficiently investigated. This study investigates the influence of samarium (Sm3+) doping on the structural and in vitro bioactive behavior of two Hench-type glasses, S53P4 and 13–93, containing 0.2 and 2 mol% Sm2O3. Structural characterization by MAS-NMR, FTIR, and Raman spectroscopy reveals that Sm3+ promotes silicate network depolymerization by generating non-bridging oxygens. Despite this depolymerization, Sm-doped glasses show reduced ion release (up to 20 % reduction in Ca and Si after 24 h), and lower pH changes (maximum pH 7.8 vs. 8.4 in the undoped glass), and a delayed hydroxycarbonate apatite (HCA) formation in simulated body fluid (SBF). These effects are attributed to strong Smsingle bondO bonding and restricted ion mobility in the glass network. The findings indicate that Sm3+ modifies the glass network and influences dissolution kinetics, providing clearer insight into the structure–bioactivity relationship in REE-doped silicate glasses. This combined behavior may be used to guide the design of compositions with controlled degradation for regenerative applications.

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