摘要
The development of advanced biomaterials is crucial for addressing the increasing demand for improved medical implants and tissue engineering scaffolds. Hydroxyapatite (HAp), a naturally occurring mineral form of calcium apatite, is widely recognized for its excellent biocompatibility and osteoconductivity, making it an ideal candidate for bone-related applications. However, its brittleness and lack of flexibility limit its broader application in dynamic biological environments. To overcome these limitations, this study explores the synthesis of Hydroxyapatite/Alginate (HAp/Alg) nanocomposites, leveraging the biocompatibility and flexibility of alginate—a natural polysaccharide derived from brown seaweed. The HAp/Alg nanocomposites were synthesized using in situ hybridization techniques with varying alginate concentrations (10 to 40 wt%) to optimize their structural and functional properties. The motivation behind this work lies in the potential of these composites to combine the desirable properties of both HAp and alginate, resulting in a material that not only mimics the mineral composition of bone but also offers enhanced flexibility and structural integrity. A comprehensive analysis was conducted using X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric Analysis/Differential Thermal Analysis (TGA/DTA), Scanning Electron Microscopy (SEM), and cytotoxicity testing to evaluate the structural, chemical, and biological properties of the composites. XRD analysis indicated a complex interaction between alginate concentration and crystal growth, with crystallite size increasing up to 10 wt% alginate before decreasing. FT-IR spectra confirmed significant biological reactivity at the composite’s surface and within the polymer matrix, suggesting strong potential for biological interactions. SEM images revealed a more uniform microstructure in HAp/Alg composites compared to pure HAp, which is likely to improve their performance in biomedical applications. TGA/DTA results demonstrated the thermal stability of the composites across various temperature conditions, while cytotoxicity tests confirmed their biocompatibility, making them suitable for use in medical applications. This study not only successfully synthesizes HAp/Alg nanocomposites with enhanced structural uniformity and biocompatibility but also provides a promising avenue for the development of next-generation biomaterials that could significantly impact the field of regenerative medicine and biomedical engineering.
The development of advanced biomaterials is crucial for addressing the increasing demand for improved medical implants and tissue engineering scaffolds. Hydroxyapatite (HAp), a naturally occurring mineral form of calcium apatite, is widely recognized for its excellent biocompatibility and osteoconductivity, making it an ideal candidate for bone-related applications. However, its brittleness and lack of flexibility limit its broader application in dynamic biological environments. To overcome these limitations, this study explores the synthesis of Hydroxyapatite/Alginate (HAp/Alg) nanocomposites, leveraging the biocompatibility and flexibility of alginate—a natural polysaccharide derived from brown seaweed. The HAp/Alg nanocomposites were synthesized using in situ hybridization techniques with varying alginate concentrations (10 to 40 wt%) to optimize their structural and functional properties. The motivation behind this work lies in the potential of these composites to combine the desirable properties of both HAp and alginate, resulting in a material that not only mimics the mineral composition of bone but also offers enhanced flexibility and structural integrity. A comprehensive analysis was conducted using X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric Analysis/Differential Thermal Analysis (TGA/DTA), Scanning Electron Microscopy (SEM), and cytotoxicity testing to evaluate the structural, chemical, and biological properties of the composites. XRD analysis indicated a complex interaction between alginate concentration and crystal growth, with crystallite size increasing up to 10 wt% alginate before decreasing. FT-IR spectra confirmed significant biological reactivity at the composite’s surface and within the polymer matrix, suggesting strong potential for biological interactions. SEM images revealed a more uniform microstructure in HAp/Alg composites compared to pure HAp, which is likely to improve their performance in biomedical applications. TGA/DTA results demonstrated the thermal stability of the composites across various temperature conditions, while cytotoxicity tests confirmed their biocompatibility, making them suitable for use in medical applications. This study not only successfully synthesizes HAp/Alg nanocomposites with enhanced structural uniformity and biocompatibility but also provides a promising avenue for the development of next-generation biomaterials that could significantly impact the field of regenerative medicine and biomedical engineering.
作者
Suraya Sabrin Soshi
Syeda Kariumnnesa
Mohammad Abdul Gafur
Suraya Sabrin Soshi;Syeda Kariumnnesa;Mohammad Abdul Gafur(Department of Mechanical and Production Engineering, Ahsanullah University of Science and Technology, Dhaka, Bangladesh;Department of Physics, University of Chittagong, Chittagong, Bangladesh;Bangladesh Council of Scientific and Industrial Research, Dhaka, Bangladesh)
