Synthesis Of Biomaterials Research Articles

Deep eutectic solvents in analysis, delivery and chemistry of pharmaceuticals.

Deep eutectic solvents (DES) have an emerging scientific role, assisting modern pharmaceutics. They are uniquely supporting the resolution of crucial issues, such as the effective extraction and isolation of bio-actives. They act as media and catalysts for pharmaceutical drug synthesis, and as green solvents and modifiers in pharmaceutical analysis. Their role in pharmaceutical formulation and drug delivery is also up-and-coming, for instance, as alternative drug-solubilizing agents, drug stabilizers and functional additives, as therapeutic deep eutectic solvents, deep eutectic API, and monomers and reaction media for the synthesis of biomaterials for advanced drug delivery. The DES also help transforming medicinal/pharmaceutical chemistry. Although DES were described in 1918, their first pharmaceutical use is only reported in 1960. In view of their broad applicability in pharmaceutics, it may be interesting to review their history, origin, evolution, potential advantages, limitations, and specific applications as green solvents. A chronological and comparative study of the literature showed the important role of DES in green approaches for modern pharmaceuticals. The concepts, applications, and outcomes of DES in pharmaceutical analysis, formulation/drug delivery, and pharmaceutical/medicinal chemistry are presented. A comprehensive outline of the atypical applications of DES as effective green solvents in pharmaceutical bioactive extraction was assessed. Efforts to present classifications of DES explored in pharmaceuticals were also made. The present manuscript also covers computational trend, adds on commercial aspects with potential future applications of DES in pharmaceutical sciences.

Eliminating aqueous effluents with low-cost bioadsorbents: adsorbent characterization and mechanistic removal studies

This study focused on the synthesis and preparation of cationic and anionic biomaterials. These materials were used as adsorbents in waters polluted by various adsorbates likely to be present in the environment. Using a batch adsorption approach, this work interprets biomass Pumpkin Seed Shells (PS) as an inexpensive, environmentally benign, and promising adsorbent for 4-nitrophenol (4NP) adsorption from aqueous solution. X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and Brunauer Emmett Teller (BET) spectroscopy were among the methods used to characterize the produced biosorbent. Batch experiments were conducted based on various process factors, such as temperature, pH, concentration, contact time, and material dose. Very excellent results were obtained with a pH of 6.5, a biosorbent dosage of 0.030 g, an initial 4-nitrophenol concentration of 30 mg/L, and a temperature of 25°C.and 298 K, which were ideal for removing 4NP. 97.95% sorption was the maximum. Adsorption data better fit the Freundlich, Temkin, Liu, and Langmuir isotherms. It was demonstrated that the biosorption process is spontaneous and exothermic and that the rate of sorption obeys the Elovich and pseudo-second-order kinetics.This article explains how to create inexpensive, environmentally friendly adsorbents and looks at how well they can remove 4-nitrophenol from wastewater. The unaltered biochar-based pumpkin seed shells were characterized using basic analysis, FTIR, SEM, and BET.

Integrating AI with Chemical Engineering for Rapid Biomaterial Development in Health Applications

This research presents an innovative approach to healthcare biomaterial development by integrating AI with chemical engineering methodologies. This study combines AI’s predictive power with the precision of chemical engineering to accelerate the discovery and optimization of biomaterials tailored for health applications while focusing on biocompatibility, adaptability, and stringent biomedical functionality. By using machine learning frameworks and advanced simulation software, the project developed predictive models that streamline biomaterial synthesis. This reduced experimental cycles by up to 40% and shortened development timelines by over 30%. Through neural networks and hybrid AI models, material properties such as degradation rate, strength, and biocompatibility can be accurately predicted, which minimizes in vivo testing and accelerates the transition from laboratory research to clinical trials. Protocols optimized through AI-driven insights enhance biomaterial production’s reproducibility and scalability while reducing material costs by 20%, which supports economically viable synthesis methods for large-scale applications. This research contributes a customizable AI framework for health-focused biomaterial solutions and impacts areas such as regenerative medicine, drug delivery, and implantable devices. Future directions include integrating real-time clinical feedback into AI models to improve safety and adaptability, thus advancing sustainable and personalized approaches to biomaterial development. This interdisciplinary framework demonstrates how AI-enhanced chemical engineering workflows can yield adaptive biomaterials suited to specific biomedical needs and offers unprecedented precision in material selection. The model’s high predictive accuracy in biocompatibility screening, achieving over 90%, enables focused experimental validation while reducing the need to rely on animal studies, which fosters ethical research practices. The sustainability impact of this project is significant, as AI-driven optimization reduces resource consumption and waste and aligns with eco-friendly biomaterial development practices. Ultimately, this research paves the way for rapid, efficient, and sustainable innovations in healthcare materials and sets a foundation for future advancements in personalized medical applications.

Open-vessel polymerization of N-carboxyanhydride (NCA) for polypeptide synthesis.

Synthetic polypeptides, also known as poly(α-amino acids), have the same polyamide backbone structures as natural proteins and peptides. As an important class of biomaterials, polypeptides have been widely used because of their biocompatibility, bioactivity and biodegradability. Ring-opening polymerization of N-carboxyanhydride (NCA) is a classical and widely used method for the synthesis of polypeptides. The dominantly used primary amine-initiated NCA polymerization can yield well-defined polymers and complex macromolecular architectures, but the reaction is slow and sensitive to moisture, making it necessary to use anhydrous solvents and a glovebox. One solution is to use lithium hexamethyldisilazide (LiHMDS) as the initiator, as described in this protocol. LiHMDS-initiated NCA polymerization is less sensitive to moisture and can be carried out in an open vessel outside the glovebox. It is also very fast; the reaction can be complete within 5 min to produce 30-mer polypeptides. In this protocol, poly(γ-benzyl-L-glutamate) is prepared as an example, but the protocol can easily be adapted to the synthesis of other polypeptides by generating NCAs from different amino acids, making it particularly suitable for the efficient parallel synthesis of polypeptide libraries. We provide detailed procedures for NCA synthesis and purification, the method of polymer end-group modification and measurement of polymerization kinetics and reactivity ratio. The procedure for synthesis of monomers and polymerization to form polypeptides requires <1 d. The superfast and open-vessel NCA polymerization method described here will probably enable a wide range of applications in the synthesis and functional study of polypeptide biomaterials.

A terphenyl derivative-based colorimetric-fluorimetric probe for the detection of lysine and arginine and their bioimaging

Lysine (Lys) and arginine (Arg) play a crucial role in the human diets, medical diagnostics, and functional biomaterial synthesis. The imbalance of intake for these two amino acids causes various diseases. Although many analytical techniques have been reported for the detection of amino acids, there are still some issues such as the need for bulky instruments, professional operators, sensitivity to be improved, and real-time detection. Here, a novel colorimetric-fluorimetric probe based on a terphenyl derivative (TPT) has been synthesized for the precise detection of Lys and Arg. In the EtOH-H2O solution of TPT, the NH2 group at the chain end of Lys/Arg undergoes a nucleophilic addition reaction with CN groups of benzothiazole groups of the probe TPT, which breaks the initial long-conjugated system of the probe molecule. As a result, blue shifts can be observed for both UV–vis absorption spectra and fluorescence spectra, accompanying with color changes of the TPT solution. The UV–vis absorption peak of TPT solution shifts from ∼410 nm to ∼325 nm, and the solution color changes from light-yellow to colorless. The fluorescence emission shifts from ∼580 nm to ∼470 nm and the bright-yellow TPT solution changes to blue under the irradiation of 365 nm UV light. For colorimetric method, the limits of detection (LoD) are 0.82 μM and 0.90 μM for Lys and Arg, respectively. For fluorimetric method, they are 2.02 nM and 1.62 nM for Lys and Arg, respectively. In addition, TPT has good selectivity and anti-interference for Lys and Arg. The synthesized probe TPT has been successfully used for the precise detection of Lys and Arg in drugs and for fluorescence imaging of living cells. This work demonstrates that terphenyl-based derivatives are promising organic probes for the detection of Lys and Arg, providing a new way for designing other amino acids probes.

Recent Advances in the Biosynthesis of Mid- and Long-Chain Dicarboxylic Acids Using Terminally Oxidizing Unconventional Yeasts.

As high-performance monomers for the manufacture of polyamide materials, mid- and long-chain dicarboxylic acids (DCAi, i ≥ 6) have received extensive attention from researchers. Biosynthesis is gradually replacing chemical synthesis due to its outstanding advantages in the industrial production of mid- and long-chain dicarboxylic acids, which is mostly achieved by using the strong terminal oxidation ability of nonmodel microorganisms such as Candida tropicalis to oxidize hydrophobic substrates such as alkanes. Here, we first summarize the metabolic pathways of oxidative alkane conversion into dicarboxylic acid by terminally oxidizing unconventional yeasts and the corresponding metabolic engineering strategies. Then, we summarize the research progress on new dicarboxylic acid production processes. Finally, the future development directions in the biosynthesis of mid- and long-chain dicarboxylic acids are prospected from synthetic biology and bioprocess engineering, which can also provide a reference for the synthesis of other biobased chemicals and biomaterials.

Microwave Revolution: Transforming Biomedical Synthesis for Tissue Engineering Advancements

: Microwave-Assisted Synthesis (MAS) has emerged as a groundbreaking technique revolutionizing the field of biomedical and tissue engineering. This review aims to explore the fundamental principles, techniques, and applications of MAS in these domains. Beginning with an overview highlighting its significance, we delve into the basic principles, mechanisms, and comparative analysis with conventional methods. Subsequently, the review explores MAS techniques in biomaterial synthesis, tissue scaffold fabrication, functionalization, and nanomaterial synthesis, along with their role in drug delivery systems. We then examine its diverse applications, including rapid biomaterial synthesis, property tailoring, biocompatibility enhancements, and tissue regeneration strategies. Furthermore, we address the challenges and future perspectives, focusing on safety considerations, understanding cellular responses, integration with advanced technologies, regulatory aspects, and future directions. This comprehensive review underscores MAS as a transformative tool driving innovations in biomedical research and therapeutic applications.

Tailor-Made Polysaccharides for Biomedical Applications.

Polysaccharides (PSAs) are carbohydrate-based macromolecules widely used in the biomedical field, either in their pure form or in blends/nanocomposites with other materials. The relationship between structure, properties, and functions has inspired scientists to design multifunctional PSAs for various biomedical applications by incorporating unique molecular structures and targeted bulk properties. Multiple strategies, such as conjugation, grafting, cross-linking, and functionalization, have been explored to control their mechanical properties, electrical conductivity, hydrophilicity, degradability, rheological features, and stimuli-responsiveness. For instance, custom-made PSAs are known for their worldwide biomedical applications in tissue engineering, drug/gene delivery, and regenerative medicine. Furthermore, the remarkable advancements in supramolecular engineering and chemistry have paved the way for mission-oriented biomaterial synthesis and the fabrication of customized biomaterials. These materials can synergistically combine the benefits of biology and chemistry to tackle important biomedical questions. Herein, we categorize and summarize PSAs based on their synthesis methods, and explore the main strategies used to customize their chemical structures. We then highlight various properties of PSAs using practical examples. Lastly, we thoroughly describe the biomedical applications of tailor-made PSAs, along with their current existing challenges and potential future directions.

Synthesis and Characterization of Triticale Starch-Based Hydrogel for pH Responsive Controlled Diffusion.

Considering the FAO perspectives for agriculture toward 2030, many natural sources will be no longer profitable for the synthesis of many biomaterials. Triticale (X Triticosecale Wittmack) is a cereal crop synthesized to withstand those marginal conditions; however, it is primarily used as fodder worldwide. We reported for the first time the synthesis of a natural anionic hydrogel with gastrointestinal pH stimulus-response as a new alternative of smart material, based on Eronga triticale starch as sustainable biomass, using citrate (pK a ∼3.1, 4.7, and 6.4) as cross-linking agent. The scanning electron microscopy and X-ray diffraction exhibited A and B-type starch granules, and semicrystallinity A-type. The presence of the anionic sensing group (COOH) was verified by infrared spectroscopy, the interactions by hydrogen bonds between starch and glycerol and esterification between starch and citric acid were identified by 1H NMR spectra, and through thermal analysis hydrogels exhibited four endothermic curves (179-319 °C, ∼0.711-39 kJ/mol E a). The results showed that the slight addition of glycerol increases the thermal stability, but a higher amount of glycerol decreases the intermolecular forces affecting the thermal stability contrary, the mechanical properties could be benefited. The rheological analyses showed viscoelastic tendency (G' > G″) with high stability (Tanδ < 1) in frequency, time, and strain sweeps. Gastrointestinal pH sensitivity (∼2-7.8) was verified (α ≤ 0.01) following Fick's diffusive parameters, which resulted in a tendency to gradually release BSA with increasing pH ∼3-7 by anomalous and case-II diffusion, showing greater release at pH ∼7.8/3.5 h (80-96%). We aim to expand the biomaterials area focusing on triticale starch due to its limited reported investigations, low-cost, green modification, and its rheological performance as plastic.

A study on tung oil-infused polyurea microcapsules: Prioritizing self-healing with bioassay-based toxicity and antibiofilm evaluations

This study presents a novel approach to enhancing the longevity and efficacy of dental materials through the incorporation of Tung oil into polyurea microcapsule coatings. Tung oil is renowned for its superior moisture barrier and antimicrobial properties, and when merged with the durable nature of polyurea, it creates a coating poised to substantially improve self-healing capabilities in dental applications. Focusing on the dual objectives of mechanical fortitude and biocompatibility, this research meticulously evaluates the coatings' proficiency in withstanding the rigors of the oral environment and their compatibility with oral tissues. Employing a suite of bioassays, we meticulously assess the toxicity and antibiofilm characteristics of these coatings, in addition to their self-healing efficiency. These evaluations measure the coatings’ ability to autonomously repair physical damage and counteract microbial colonization. The results reveal that tung oil significantly enhances the polyurea matrix's intrinsic self-repair features, which proves crucial in resisting the abrasive and microbial challenges prevalent in the oral cavity. The modified coatings demonstrate marked improvements in wear resistance and microbial interaction, heralding a significant advancement in dental material technology. This in-depth analysis corroborates the amplified capabilities of Tung oil-infused polyurea coatings and paves the way for future investigations into the integration of natural oils within medical-grade material design, opening a new chapter in the synthesis of biomaterials tailored for oral healthcare advancements.

INTELLIGENT INFORMATION TECHNOLOGIES TO SUPPORT DECISION-MAKING WHEN APPLYING THE CAD/CAM/CAE SYSTEM OF DESIGN AND USING ADDITIVE TECHNOLOGIES

The direction of research is the development of principles and methods for making scientifically based decisions in the design and additive manufacturing of bone substitutes based on apatite-biopolymer composites with functional properties depending on the nature of the localization of the cavity bone defect and its size. The relevance is due to the fact that the development of an intelligent decision-making support system based on neural network modeling, the development of methods for their training, tabagato-criterion optimization of design processes, will allow the creation of three-dimensional solid models of defects taking into account their spatial structure and bone substitutes for the synthesis of biomaterials with controlled composition, porosity and mechanical strength, which are optimal for a specific area of bone replacement, which will increase the effectiveness of treatment and prosthetics in orthopedics and traumatology. A set of methods for analyzing images of bone tissue, taking into account its spatial structure, which are obtained by sensors of different physical nature, with the use of neural network models, development of methods of their design, optimization, and training is proposed. A modification of the method of learning neural networks based on gradient descent, based on the application of the theory of nonlinear dynamics, is proposed. Corresponding theoretical provisions have been developed.

Incorporation of Multiple β2-Hydroxy Acids into a Protein In Vivo Using an Orthogonal Aminoacyl-tRNA Synthetase.

The programmed synthesis of sequence-defined biomaterials whose monomer backbones diverge from those of canonical α-amino acids represents the next frontier in protein and biomaterial evolution. Such next-generation molecules provide otherwise nonexistent opportunities to develop improved biologic therapies, bioremediation tools, and biodegradable plastic-like materials. One monomer family of particular interest for biomaterials includes β-hydroxy acids. Many natural products contain isolated β-hydroxy acid monomers, and polymers of β-hydroxy acids (β-esters) are found in polyhydroxyalkanoate (PHA) polyesters under development as bioplastics and drug encapsulation/delivery systems. Here we report that β2-hydroxy acids possessing both (R) and (S) absolute configuration are substrates for pyrrolysyl-tRNA synthetase (PylRS) enzymes in vitro and that (S)-β2-hydroxy acids are substrates in cellulo. Using the orthogonal MaPylRS/MatRNAPyl synthetase/tRNA pair, in conjunction with wild-type E. coli ribosomes and EF-Tu, we report the cellular synthesis of model proteins containing two (S)-β2-hydroxy acid residues at internal positions. Metadynamics simulations provide a rationale for the observed preference for the (S)-β2-hydroxy acid and provide mechanistic insights that inform future engineering efforts. As far as we know, this finding represents the first example of an orthogonal synthetase that acylates tRNA with a β2-hydroxy acid substrate and the first example of a protein hetero-oligomer containing multiple expanded-backbone monomers produced in cellulo.

Hydrothermally doping valve metal Nb into Titanate nanofibers structure for potentially engineering bone tissue

Recent research efforts in bone tissue engineering have been primarily directed towards manufacture-viable synthesis of biomaterials that can significantly enhance the biocompatibilities and osteogenic capabilities on the new biomaterials. This paper presents a straightforward, cost-effective, optimized, and well-controlled hydrothermal synthesis of Nb-doped potassium titanate nanofibers in high-purity. Characterization data revealed that the Nb-doping potassium titanate maintained the crystal structure, showing great promise for applications in bone tissue engineering.

Transcriptomic Insights into Metabolism-Dependent Biosynthesis of Bacterial Nanocellulose.

Bacterial nanocellulose (BNC) is an attractive green-synthesized biomaterial for biomedical applications and various other applications. However, effective engineering of BNC production has been limited by our poor knowledge of the related metabolic processes. In contrast to the traditional perception that genome critically determines biosynthesis behaviors, here we discover that the glucose metabolism could also drastically affect the BNC synthesis in Gluconacetobacter hansenii. The transcriptomic profiles of two model BNC-producing strains, G. hansenii ATCC 53582 and ATCC 23769, which have highly similar genomes but drastically different BNC yields, were compared. The results show that their BNC synthesis capacities were highly related to metabolic activities such as ATP synthesis, ion transport protein assembly, and carbohydrate metabolic processes, confirming an important role of metabolism-related transcriptomes in governing the BNC yield. Our findings provide insights into the microbial biosynthesis behaviors from a transcriptome perspective, potentially guiding cellular engineering for biomaterial synthesis.

Degradable and Multifunctional PEG-Based Hydrogels Formed by iEDDA Click Chemistry with Stable Click-Induced Supramolecular Interactions.

The inverse electron demand Diels-Alder (iEDDA) reactions are highly efficient click chemistry increasingly utilized in bioconjugation, live cell labeling, and the synthesis and modification of biomaterials. iEDDA click reactions have also been used to cross-link tetrazine (Tz) and norbornene (NB) modified macromers [e.g., multiarm poly(ethylene glycol) or PEG]. In these hydrogels, Tz-NB adducts exhibit stable supramolecular interactions with a high hydrolytic stability. Toward engineering a new class of PEG-based click hydrogels with highly adaptable properties, we previously reported a new group of NB-derivatized PEG macromers via reacting hydroxyl-terminated PEG with carbic anhydride (CA). In this work, we show that hydrogels cross-linked by PEGNBCA or its derivatives exhibited fast and tunable hydrolytic degradation. Here, we show that PEGNBCA (either mono- or octafunctional) and its dopamine or tyramine conjugated derivatives (i.e., PEGNB-D and PEGNB-T) readily cross-link with 4-arm PEG-Tz to form a novel class of multifunctional iEDDA click hydrogels. Through modularly adjusting the macromers with unstable and stable iEDDA click-induced supramolecular interactions (iEDDA-CSI), we achieved highly tunable degradation, with full degradation in less than 2 weeks to over two months. We also show that secondary enzymatic reactions could dynamically stiffen these hydrogels. These hydrogels could also be spatiotemporally photopatterned through visible light-initiated photochemistry. Finally, the iEDDA-CSI hydrogels post ester hydrolysis displayed shear-thinning and self-healing properties, enabling injectable delivery.

Hydrogels based on lignin extracted from cashew apple bagasse and its application in antimicrobial wound dressings

Hydrogels are versatile materials with a three-dimensional network structure that can retain water and release bioactive compounds. They have found applications in various fields, including agriculture, biomaterial synthesis, and pharmaceuticals. Incorporating natural antimicrobial compounds into hydrogels is a promising approach to developing non-toxic biomedical materials, particularly for wound healing dressings. It was evaluated the extraction and use of cashew apple bagasse lignin (CAB-Lig) due to its healing, anti-inflammatory, and antimicrobial properties for producing a hydrogel-based bandage. The extraction process involved acid and alkali treatments followed by precipitation. The antimicrobial potential of CAB-Lig was evaluated at different concentrations for formulating hydrogels. Hydrogels containing 0.1 % and 3 % lignin showed high swelling and liquid retention abilities. The 3 % lignin hydrogel exhibited effectiveness against Escherichia coli and Staphylococcus aureus. Incorporating CAB-Lig into the hydrogel structure improved its mechanical properties, making it more suitable for application as a bandage. Moreover, the extracted lignin showed low toxicity, indicating its safe use. A bandage was formulated by combining the CAB-Lig-based hydrogel with polyester, which possessed antimicrobial properties and demonstrated biocompatibility (L929 and HaCat cells). The results confirmed the potential of CAB-Lig for synthesizing hydrogels and dressings with antimicrobial properties, offering a sustainable solution for utilizing lignocellulosic biomass.

Understanding plant growth using automation approaches for biomaterial synthesis

Understanding plant growth using automation approaches for biomaterial synthesis

Solvent-free synthesis of biostable segmented polyurethane shape memory polymers for biomedical applications.

Biostable shape memory polymers that remain stable in physiological conditions are beneficial for user-defined shape recovery in response to a specific stimulus. For potential commercialization and biocompatibility considerations, biomaterial synthesis must be simple and scalable. Hence, a library of biostable and cytocompatible shape memory polymers with tunable thermomechanical properties based on hard segment content was synthesized using a solvent-free method. Polymer surface chemistry, thermomechanical and shape memory properties, and biostability were assessed. We also investigated the effects of processing methods on thermomechanical and shape memory properties. All polymers showed high glass transition temperatures (>50 °C), which indicates that their temporary shape could be preserved after implantation. Polymers also demonstrate high shape fixity (73-80%) and shape recovery (93-95%). Minimal mass loss (<5%) was observed in accelerated oxidative (20% H2O2) and hydrolytic (0.1 M NaOH) media. Additionally, minimal shape recovery (∼0%) occurred in programmed samples with higher hard segment content that were stored in degradation media. After 40 days of storage in media, programmed samples recovered their primary shapes upon heating to temperatures above their transition temperature. Annealing to above the polymer melting point and solvent casting of polymers improved shape memory and thermal properties. To enable their potential use as biomaterial scaffolds, fiber formation of synthesized polyurethanes was compared with those of samples synthesized using a previously reported solvent-based method. The new method provided polymers that can form fibrous scaffolds with improved mechanical and shape memory properties, which is attributed to the higher molecular weight and crystalline content of polymers synthesized using the new, solvent-free approach. These biostable segmented polyurethanes could be coupled with a range of components that respond to specific stimuli, such as enzymes, magnetic field, pH, or light, to enable a specific shape change response, which could be coupled with drug and/or bioactive material delivery in future work.

Animal models, treatment options, and biomaterials for female stress urinary incontinence.

In the quest to tackle stress urinary incontinence (SUI), the synthesis of cutting-edge biomaterials and regenerative materials has emerged as a promising frontier. Briefly, animal models like vaginal distension and bilateral ovariectomy serve as crucial platforms for unraveling the intricacies of SUI, facilitating the evaluation of innovative treatments. The spotlight, however, shines on the development and application of novel biomaterials-ranging from urethral bulking agents to nano-gel composites-which aim to bolster urethral support and foster tissue regeneration. Furthermore, the exploration of stem cell therapies, particularly those derived from adipose tissues and urine, heralds a new era of regenerative medicine, offering potential for significant improvements in urinary function. This review encapsulates the progress in biomaterials and regenerative strategies, highlighting their pivotal role in advancing the treatment of SUI, thereby opening new avenues for effective and minimally invasive solutions.

Synthesis and mechanical characterization of hydroxyapatite-based biomaterials reinforced with nickel-titanium-magnesium alloys for use in cortical bone implants

In this work, biomaterials consisting of bioactive hydroxyapatite-based ceramic and nickel-titanium-magnesium alloys were made. The biomaterials were obtained through powder techniques involving mechanical milling, uniaxial pressing and pressureless sintering. The purpose of the study was to evaluate the effect of alloys on the mechanical properties of hydroxyapatite, the alloy additions were 0, 20, 30, 40, 40, 50 and 60 wt.%. The results were compared with cortical bone samples of bovine origin. From the results, it is possible to comment that, with increasing alloy contents in the hydroxyapatite, the mechanical properties increase considerably. The behavior of the composites reinforced with 50 and 60 wt.% NiTiMg alloy is similar to that of bovine cortical bone. The microstructures of the biomaterials are fine, homogeneous, and similar to those of bovine cortical bone. From the study it can be commented that given the mechanical characteristics of the biomaterials obtained, they could be used as possible bone implants.