Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural Properties

Bone substitute materials require specific properties to make them suitable for implantation, such as biocompatibility and resistance to mechanical loads. Mg,Sr-cosubstituted hydroxyapatite (MgSr-HA) is a promising bone scaffold candidate because its structure is similar to the native bone matrix. H...

Full description

Bibliographic Details
Main Authors: Elena Landi, Stefano Guizzardi, Elettra Papa, Carlo Galli
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/11/11/4930
_version_ 1797532482149548032
author Elena Landi
Stefano Guizzardi
Elettra Papa
Carlo Galli
author_facet Elena Landi
Stefano Guizzardi
Elettra Papa
Carlo Galli
author_sort Elena Landi
collection DOAJ
description Bone substitute materials require specific properties to make them suitable for implantation, such as biocompatibility and resistance to mechanical loads. Mg,Sr-cosubstituted hydroxyapatite (MgSr-HA) is a promising bone scaffold candidate because its structure is similar to the native bone matrix. However, MgSr-HA materials do not typically withstand thermal treatments over 800 °C, because Mg promotes HA degradation to less stable tricalcium phosphate, a compound that, albeit biocompatible, is not found in bone. We, therefore, designed an ion-exchange process to enrich sintered Sr-HA with Mg and obtain MgSr-HA porous constructs. These materials contained a 0.04–0.08 Mg/Ca molar ratio and a 0.12–0.13 Sr/Ca molar ratio, and had up to 20 MPa of compressive strength, suitable for use as bone fillers or scaffolds. Unlike previous synthetic Mg,Sr-substituted apatite powders, the proposed process did not degrade HA and thus preserved its similarity to bone structure. The obtained material thus combines the presence of bioactive Mg and Sr ions in the HA lattice with a 3D morphological/structural organization that can be customized in pore size and distribution, as well as in mechanical strength, thus potentially covering a wide range of clinical applications.
first_indexed 2024-03-10T10:59:47Z
format Article
id doaj.art-c46bb9cd82de476da0c903007ce82507
institution Directory Open Access Journal
issn 2076-3417
language English
last_indexed 2024-03-10T10:59:47Z
publishDate 2021-05-01
publisher MDPI AG
record_format Article
series Applied Sciences
spelling doaj.art-c46bb9cd82de476da0c903007ce825072023-11-21T21:37:19ZengMDPI AGApplied Sciences2076-34172021-05-011111493010.3390/app11114930Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural PropertiesElena Landi0Stefano Guizzardi1Elettra Papa2Carlo Galli3ISTEC-CNR, Institute of Science and Technology for Ceramics-National Research Council, Via Granarolo 64, 48018 Faenza, ItalyDiMeC, Department of Medicine and Surgery, University of Parma, Via Volturno 39, 43126 Parma, ItalyISTEC-CNR, Institute of Science and Technology for Ceramics-National Research Council, Via Granarolo 64, 48018 Faenza, ItalyDiMeC, Department of Medicine and Surgery, University of Parma, Via Volturno 39, 43126 Parma, ItalyBone substitute materials require specific properties to make them suitable for implantation, such as biocompatibility and resistance to mechanical loads. Mg,Sr-cosubstituted hydroxyapatite (MgSr-HA) is a promising bone scaffold candidate because its structure is similar to the native bone matrix. However, MgSr-HA materials do not typically withstand thermal treatments over 800 °C, because Mg promotes HA degradation to less stable tricalcium phosphate, a compound that, albeit biocompatible, is not found in bone. We, therefore, designed an ion-exchange process to enrich sintered Sr-HA with Mg and obtain MgSr-HA porous constructs. These materials contained a 0.04–0.08 Mg/Ca molar ratio and a 0.12–0.13 Sr/Ca molar ratio, and had up to 20 MPa of compressive strength, suitable for use as bone fillers or scaffolds. Unlike previous synthetic Mg,Sr-substituted apatite powders, the proposed process did not degrade HA and thus preserved its similarity to bone structure. The obtained material thus combines the presence of bioactive Mg and Sr ions in the HA lattice with a 3D morphological/structural organization that can be customized in pore size and distribution, as well as in mechanical strength, thus potentially covering a wide range of clinical applications.https://www.mdpi.com/2076-3417/11/11/4930apatite synthesissinteringion exchangeporous scaffoldcharacterization
spellingShingle Elena Landi
Stefano Guizzardi
Elettra Papa
Carlo Galli
Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural Properties
Applied Sciences
apatite synthesis
sintering
ion exchange
porous scaffold
characterization
title Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural Properties
title_full Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural Properties
title_fullStr Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural Properties
title_full_unstemmed Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural Properties
title_short Mg,Sr-Cosubstituted Hydroxyapatite with Improved Structural Properties
title_sort mg sr cosubstituted hydroxyapatite with improved structural properties
topic apatite synthesis
sintering
ion exchange
porous scaffold
characterization
url https://www.mdpi.com/2076-3417/11/11/4930
work_keys_str_mv AT elenalandi mgsrcosubstitutedhydroxyapatitewithimprovedstructuralproperties
AT stefanoguizzardi mgsrcosubstitutedhydroxyapatitewithimprovedstructuralproperties
AT elettrapapa mgsrcosubstitutedhydroxyapatitewithimprovedstructuralproperties
AT carlogalli mgsrcosubstitutedhydroxyapatitewithimprovedstructuralproperties