Hamza Elbaza , Hanaa Mabroum , Yousra Hamdan , Rachid El Fatimy , Sanae Ben Mkaddem , Hicham Ben youcef , Allal Barroug , Hassan Noukrati
{"title":"原位合成多糖稳定的无定形磷酸钙:力学性能和体外生物学评价","authors":"Hamza Elbaza , Hanaa Mabroum , Yousra Hamdan , Rachid El Fatimy , Sanae Ben Mkaddem , Hicham Ben youcef , Allal Barroug , Hassan Noukrati","doi":"10.1016/j.coco.2025.102436","DOIUrl":null,"url":null,"abstract":"<div><div>The short lifetime and the weak mechanical properties of amorphous calcium phosphate-based materials (ACP) constitute the most relevant drawbacks prohibiting their use for orthopedic application. The current study focuses on the <em>in-situ</em> synthesis of ACP composite using sodium alginate and/or chitosan as biopolymers to address these drawbacks. The prepared composites were characterized using XRD, FTIR, SEM, and TGA-DTA. The formulated composites using alginate (ACP<sub>Alg</sub>), chitosan (ACP<sub>CS</sub>), and alginate-chitosan (ACP<sub>Alg-CS</sub>) exhibited an amorphous structure typical of the amorphous nature of the ACP phase. The evolution of the precipitated amorphous phase as a function of the maturation time indicated that polymer-free ACP is stable only for 5 min. However, adding the polysaccharides increases the amorphous phase lifetime from 5 min to 2 h, thus raising its stability. The TGA-DTA analysis demonstrated that the presence of polymers significantly delayed the crystallization of ACP, confirming their stabilization effect. Furthermore, the polymer content in the amorphous composites estimated using TGA analysis revealed that only 6.7 wt% and 7.2 wt% of the polymeric phase were associated with the amorphous matrix in ACP<sub>Alg</sub> and ACP<sub>Alg-CS</sub>, respectively. Nevertheless, 19 wt% of chitosan polymer was successfully associated with the ACP<sub>CS</sub> matrix. The three-dimensional composites elaborated from ACP<sub>CS</sub> and ACP<sub>Alg-CS</sub> and using acetic acid as a liquid phase exhibited high compressive strength, achieving a value of 98 MPa for ACP<sub>CS</sub>-based composite. The <em>in vitro</em> bioactivity and biodegradability of the prepared biocomposites in the SBF solution were confirmed. Moreover, the cytotoxicity test of the selected composites highlighted their high biocompatibility.</div></div>","PeriodicalId":10533,"journal":{"name":"Composites Communications","volume":"57 ","pages":"Article 102436"},"PeriodicalIF":6.5000,"publicationDate":"2025-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In situ synthesis of polysaccharide-stabilized amorphous calcium Phosphate: Mechanical performance and In vitro biological assessment\",\"authors\":\"Hamza Elbaza , Hanaa Mabroum , Yousra Hamdan , Rachid El Fatimy , Sanae Ben Mkaddem , Hicham Ben youcef , Allal Barroug , Hassan Noukrati\",\"doi\":\"10.1016/j.coco.2025.102436\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The short lifetime and the weak mechanical properties of amorphous calcium phosphate-based materials (ACP) constitute the most relevant drawbacks prohibiting their use for orthopedic application. The current study focuses on the <em>in-situ</em> synthesis of ACP composite using sodium alginate and/or chitosan as biopolymers to address these drawbacks. The prepared composites were characterized using XRD, FTIR, SEM, and TGA-DTA. The formulated composites using alginate (ACP<sub>Alg</sub>), chitosan (ACP<sub>CS</sub>), and alginate-chitosan (ACP<sub>Alg-CS</sub>) exhibited an amorphous structure typical of the amorphous nature of the ACP phase. The evolution of the precipitated amorphous phase as a function of the maturation time indicated that polymer-free ACP is stable only for 5 min. However, adding the polysaccharides increases the amorphous phase lifetime from 5 min to 2 h, thus raising its stability. The TGA-DTA analysis demonstrated that the presence of polymers significantly delayed the crystallization of ACP, confirming their stabilization effect. Furthermore, the polymer content in the amorphous composites estimated using TGA analysis revealed that only 6.7 wt% and 7.2 wt% of the polymeric phase were associated with the amorphous matrix in ACP<sub>Alg</sub> and ACP<sub>Alg-CS</sub>, respectively. Nevertheless, 19 wt% of chitosan polymer was successfully associated with the ACP<sub>CS</sub> matrix. The three-dimensional composites elaborated from ACP<sub>CS</sub> and ACP<sub>Alg-CS</sub> and using acetic acid as a liquid phase exhibited high compressive strength, achieving a value of 98 MPa for ACP<sub>CS</sub>-based composite. The <em>in vitro</em> bioactivity and biodegradability of the prepared biocomposites in the SBF solution were confirmed. 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In situ synthesis of polysaccharide-stabilized amorphous calcium Phosphate: Mechanical performance and In vitro biological assessment
The short lifetime and the weak mechanical properties of amorphous calcium phosphate-based materials (ACP) constitute the most relevant drawbacks prohibiting their use for orthopedic application. The current study focuses on the in-situ synthesis of ACP composite using sodium alginate and/or chitosan as biopolymers to address these drawbacks. The prepared composites were characterized using XRD, FTIR, SEM, and TGA-DTA. The formulated composites using alginate (ACPAlg), chitosan (ACPCS), and alginate-chitosan (ACPAlg-CS) exhibited an amorphous structure typical of the amorphous nature of the ACP phase. The evolution of the precipitated amorphous phase as a function of the maturation time indicated that polymer-free ACP is stable only for 5 min. However, adding the polysaccharides increases the amorphous phase lifetime from 5 min to 2 h, thus raising its stability. The TGA-DTA analysis demonstrated that the presence of polymers significantly delayed the crystallization of ACP, confirming their stabilization effect. Furthermore, the polymer content in the amorphous composites estimated using TGA analysis revealed that only 6.7 wt% and 7.2 wt% of the polymeric phase were associated with the amorphous matrix in ACPAlg and ACPAlg-CS, respectively. Nevertheless, 19 wt% of chitosan polymer was successfully associated with the ACPCS matrix. The three-dimensional composites elaborated from ACPCS and ACPAlg-CS and using acetic acid as a liquid phase exhibited high compressive strength, achieving a value of 98 MPa for ACPCS-based composite. The in vitro bioactivity and biodegradability of the prepared biocomposites in the SBF solution were confirmed. Moreover, the cytotoxicity test of the selected composites highlighted their high biocompatibility.
期刊介绍:
Composites Communications (Compos. Commun.) is a peer-reviewed journal publishing short communications and letters on the latest advances in composites science and technology. With a rapid review and publication process, its goal is to disseminate new knowledge promptly within the composites community. The journal welcomes manuscripts presenting creative concepts and new findings in design, state-of-the-art approaches in processing, synthesis, characterization, and mechanics modeling. In addition to traditional fiber-/particulate-reinforced engineering composites, it encourages submissions on composites with exceptional physical, mechanical, and fracture properties, as well as those with unique functions and significant application potential. This includes biomimetic and bio-inspired composites for biomedical applications, functional nano-composites for thermal management and energy applications, and composites designed for extreme service environments.