1. Introduction
In recent decades, AM processes have seen widespread exploration across various sectors like aeronautics, the automotive industry, and the biomedical industry. AM relies on layer-by-layer deposition techniques, enabling the creation of intricate geometries while minimizing waste. It is particularly well-suited for producing prototypes and custom functional parts tailored to individual patients. The utilization of AM techniques for developing and fabricating implants has been extensively researched. Many medical conditions necessitate the insertion of orthopedic implants. Implants come in diverse shapes, sizes, and materials. However, it is widely acknowledged that traditional implants (mass-produced items conforming to set standards) often fail to precisely match the unique anatomy of each patient [
1,
2,
3,
4,
5]. An implant that does not fit properly can lead to sub-optimal results, compromising the patient’s healing process and the durability of the implant within the body. This is why there has been a growing interest in patient-specific implants over the past decade. Tailored precisely to match an individual’s anatomy, these implants aim to alleviate pain, reduce stress, and minimize the time required for the patient to adapt to the implant [
1,
2].
While the feasibility of producing patient-specific implants for reconstructive surgery, including orbital and craniofacial procedures, has been successfully demonstrated [
3,
6,
7], challenges arise when considering load-bearing and joint locations such as the hip, knee, ankle, and foot. These areas are subjected to substantial stress and loads, presenting more complex requirements for implant design and durability. Consequently, developing patient-specific implants for these regions necessitates meticulous attention to biomechanical factors, material selection, and manufacturing techniques, to ensure optimal performance and longevity under demanding physiological conditions [
3,
4,
5].
Despite these inherent challenges, significant strides have been made in the realm of patient-specific orthopedic implants. Numerous studies have focused on tailoring implants based on CT scans [
2,
8], while others have investigated optimal materials and 3D printing techniques for their production [
9,
10]. Notably, Hafez [
11] successfully produced a universal talus implant using innovative topological optimization methods, showcasing the potential of advanced design strategies. Similarly, Snekhalatha’s development of a patient-specific hip prosthesis via finite analysis underscored the critical role of computational modeling in implant customization [
12]. These efforts highlight the ongoing evolution of orthopedic implant technology, heralding promising advancements for improving patient outcomes and care.
Of the various 3D printing methods available, fused filament fabrication (FFF) stands out as the most popular. Its popularity stems from its user-friendly nature, extensive material options, and notably, the affordability of the printing equipment, which is often compact enough to fit on a small desktop [
13,
14]. The FFF process is illustrated in
Figure 1. In the FFF method, a thermoplastic or metallic filament (mixture of metallic particles and wax) undergoes continuous feeding into a heated chamber, where it melts. This molten material is then extruded through a nozzle and deposited layer-by-layer onto a heated table, adhering to a predefined pattern. The intended geometry is constructed along the Z-axis, as successive layers of melted filament are precisely laid down [
13,
14,
15]. Thermoplastic filaments like poly(lactic acid) (PLA) or poly(ether ether ketone) (PEEK) stand as the primary materials utilized in FFF, respectively, for common and medical applications [
13,
15,
16,
17]. However, in recent times, metallic filaments such as stainless steel, titanium, and aluminum alloys have gained increasing traction, owing to their diverse applications across various fields [
18,
19,
20].
Orthopedic implant manufacturing using fused filament fabrication (FFF) technology incorporates a variety of materials, encompassing both polymers and metallic alloys, selected based on their comprehensive mechanical properties, including strength, wear resistance, corrosion resistance, and proven bio-compatibility. Bio-compatibility is a pivotal parameter in implant development, delineating the interactions between the implant and the host environment. It is important to note that bio-compatibility is not universally standardized and can vary based on the implant’s location and the host’s response. Assessing a biomaterial’s bio-compatibility for a specific application involves conducting various tests, aiming for minimal host response across specific criteria: toxicity, mutagenicity, carcinogenicity, and immunogenicity [
21].
Polymers play a crucial role in orthopedic implant fabrication due to their biocompatibility, versatility, and ease of processing with FFF technology. Among polymers, PEEK is recognized for its exceptional mechanical properties, high temperature resistance, chemical resistance, and excellent strength [
17]. This material is often used in demanding applications where these qualities are necessary, such as aerospace, automotive applications, medical implants, and various industrial uses. Its properties make it particularly suitable for metal replacement [
13]. According to a compilation of studies as summarized by Toth [
22], PEEK demonstrates biocompatibility for bone implants and presents additional osteocompatibility. This signifies that a PEEK implant could potentially stimulate osteoblast production around the implant. Notably, PEEK showcases no chemical interactions with the host body, thereby preventing the release of ions or constituents into the host system [
23].
In addition to polymers, metallic alloys play a vital role in orthopedic implant fabrication, particularly for load-bearing applications (notably hip prosthesis) requiring high mechanical strength and durability. Stainless steel, including alloys like 316L and 17-4 PH, offers excellent corrosion resistance, mechanical properties, and biocompatibility, providing long-term stability within the host body. The 17-4 PH stainless steel alloy filament is a multipurpose steel that can be used in FFF technology. It can be heat treated to reach a hardness of 36 HRc and polished for a better surface roughness. [
19,
24,
25]. The 316L stainless steel filament is commercially designated as Ultrafuse 316L. It is one of the most common materials used in medical applications. It belongs to the family of austenitic stainless steels and offers excellent corrosion resistance, which is crucial for medical devices that come into contact with bodily fluids. [
18,
20,
21,
26]. Titanium and its alloys, such as Ti-6Al-4V and Ti-6Al-7Nb, combine low density and high bio-compatibility due to excellent corrosion resistance, making them a choice material for orthopedic implants [
27,
28], notably for hip and knee prostheses [
29], dental implants [
30], and craniofacial implants [
31]. Like steel-based implants, titanium implants can also enhance cell proliferation through the layering of specific coatings [
28,
32].
The primary objective of this study was to create a numerical solid model aimed at identifying the most suitable materials for a talus implant through simulation. Once the geometry had been generated and simplified, the optimal material (among a predefined selection) was determined based on simulation results, and it was manufactured using FFF technology. For certain materials, post-processing is required to sinter the final model or remove critical support structures. In the subsequent phase of the analysis, various materials underwent physical testing.
3. Results
3.1. Results of the Segmentation
Only bones were segmented, and
Figure 7 displays various transversal views of the segmented bones, emphasizing the talus in green. Furthermore, an isometric view of the joint is presented in the upper right quadrant, with the talus marked in purple.
Following the methodology outlined in
Section 2.2, a comparison between the original talus model and the various remeshed versions (with differing percentages of mesh reduction) was conducted. The evolution in the three criteria—average distance, mean distance, and standard deviation—with the percentage of mesh reduction is displayed in
Figure 8. Below
of mesh reduction, the values of average distance and mean distance were below 0.2 and the standard deviation was lower that 2. Between
and
of mesh reduction, the values of the three criteria rose slightly to 0.25, 0.5, and 3, respectively. These values were still acceptable, thus the impact of the remesh on the geometrical accuracy remained limited. However, starting at
reduction, the values of the three criteria underwent an exponential increase. Therefore, the critical threshold was determined to be
. For this specific study, the mesh reduction was maintained below
to guarantee optimal geometrical accuracy. The original mesh of the talus and the
-reduced version (which was used in the simulation) are displayed in
Figure 9.
3.2. Simulation Results
The successful modeling of ankle articulation enabled a comparison between various materials (PEEK, stainless steel, and titanium) and the original bone. After an unsuccessful attempt at force-driven simulation, the model was instead driven by displacements, as detailed in
Table 4. This displacement-based approach facilitated the attainment of converged solutions for each of the four movements considered in the analysis. Reaction forces in the X, Y, and Z directions, as well as the total reaction force, were computed and compared to the corresponding values for the bone.
Table 5 only presents the percentage differences between the considered material and the bone, while detailed values of the reaction forces can be found in
Appendix A.
According to the computed reaction forces, PEEK exhibited the lowest difference compared to the bones, with a maximum of for the infill. Decreasing the infill of PEEK resulted in higher but still acceptable difference values. In contrast, stainless steel and titanium showed much higher differences, reaching values up to . Stainless steel and titanium were excessively rigid compared to the behavior of the original bone material.
The magnitude of the reaction forces in the displacement-driven model corresponds to 14 times the body weight of a standard patient, equating to a safety factor of 4, for the load condition of a patient standing on one leg. This safety factor is rational, especially in scenarios where a person experiences a sudden fall from a certain height without any damping.
Fractures of the talus primarily occur at a specific location known as the neck of the talus [
52]. In alignment with this, the simulation results also revealed that the highest strains and stresses were concentrated in the neck of the talus, indicating a potential risk of fracture in this area. Equivalent strains and stresses were calculated around the neck, highlighting two distinct stress concentration zones, one at the top and another at the bottom, as illustrated in
Figure 10. The values of stress localized in the talus neck are presented in
Table 6.
Based on the stress distribution, two worst-case postures were identified: ELF and ELB. Consequently, the simulation focused specifically on these two cases. PEEK demonstrated significantly lower stress magnitudes compared to the original bone material, being less than half. In contrast, the stress in the talus models made of titanium and stainless steel was comparable to that of the bone.
It is noteworthy that the stress magnitudes for all materials surpassed their respective tensile strength, forming the basis for comparing the behavior of different materials. To address this issue and prevent excessively high stress magnitudes, material models should incorporate non-linearity, including some plasticity. The assumption is that a force equivalent to 14 times the weight of a patient can potentially lead to a fracture of the talus neck. The linear material model resulted in high stress magnitudes, and attention should also be given to the elastic strains.
Equivalent stress and strain in the neck of the talus were calculated for PEEK models with
,
, and
infill of the inner solid, to determine the optimal configuration. The Young’s modulus of fully dense PEEK was reported as 3950 MPa [
16]. For PEEK models with lower infill percentages, the Young’s modulus was obtained by multiplying the Young’s modulus of fully dense PEEK by the percentage of infill [
16]. Consequently, PEEK models with
,
, and
infill exhibited Young’s moduli of 197.5 MPa, 987.5 MPa, and 1975 MPa, respectively. The resulting Von Mises stresses are illustrated in
Figure 11. No significant difference between infill percentages was observed. The
PEEK infill showed slightly lower values compared to the other infills, although they were comparable. Additionally, the infill did not influence the location of the maximum stress values.
Elastic strain is a crucial consideration for implant assessment. The computed elastic strains of the various materials are presented for the two worst-case scenarios in
Figure 12. Focusing solely on the strain, it was indicated that a fracture of the talus under a force equivalent to 14 times the weight of the patient is unlikely. PEEK consistently exhibited values closest to those of natural bone, whereas titanium and stainless steel demonstrated a brittle behavior with an elastic strain below
. PEEK showcased a high level of flexibility, even surpassing that of bone. The computed elastic strains of PEEK remained far below the acceptable elongation at break provided by the material supplier. However, analyzing the elastic strain of PEEK for various infill values revealed no significant trend.
Consequently, PEEK emerged as a potentially suitable material for a talus implant. However, the percentage of infill remains a critical variable to determine. The stress and strain analysis did not reveal any trends regarding the optimal value of infill, but according to the computed reaction forces, a talus with infill behaved similarly to the natural bone material.
3.3. Print of the Talus Implant
Multiple specimens were 3D printed in PEEK, each with varying percentages of infill. In
Figure 13, two specimens are presented before and after heat treatment. Despite stainless steel not emerging as the optimal replacement material based on the simulation results, a few specimens were printed for evaluation. Detailed parameters of the models, including their mass, are provided in
Table 7. Mass is a critical parameter in implant development, and it should ideally align with the mass of the original bone.
According to the literature, the mass of the human talus is approximately 20 g, considering factors such as the sex, age, height, and other health considerations of the patient [
53]. PEEK implants with
infill exhibited a mass of 20.5 g, the closest value compared to the original talus. PEEK models with lower infill percentages also maintained a mass close to that of the original bone. In contrast, implants based on stainless steel weighed around 100 g, a significant deviation from the corresponding bone mass. Since titanium did not yield satisfactory results in the simulation and is expensive to print, no titanium implants were printed for weight comparison. Given the parameters selected in this study, stainless-steel-based implants seem to be the least optimal choice for talus replacement.
Taking into account the computed reaction forces, stress, and strain results, and mass, a talus with infill behaved similarly to natural bone material, making it the preferred choice for the implant material.
4. Discussion
The segmentation and simplification procedure developed for generating 3D solid numerical models has demonstrated excellent results in terms of precision and efficiency. These models are created with high accuracy and simplified to reduce the mesh size, thus decreasing the computational time without significant loss of geometric detail. Studies have shown that various smoothing algorithms, such as Laplacian smoothing, can effectively reduce mesh complexity, while preserving critical geometric features [
38,
54]. The precision of these models also allows them to be successfully 3D printed. Specifically, the implants made from PEEK with a 50% infill closely resembled the original bone structure.
Optimizing the implant surface post-treatment is crucial to enhance the relative movement of the ankle and reduce friction between the bones. This refinement aims to facilitate ligament attachment to the implant. Tailoring surface roughness is also vital for promoting cell adhesion and proliferation. Several techniques can be employed, such as sandblasting, which has been shown to enhance surface roughness, thereby improving osteoconduction, cell adhesion, bone-to-implant contact, and removal torque. These benefits support the viability of sandblasted PEEK as a bone implant [
55,
56]. Another promising technique for optimizing the surface roughness of polymeric implants is plasma coating. Studies by Wang et al. [
57] and Han et al. [
58] demonstrated that plasma coating significantly enhanced cell adhesion and proliferation. A further advancement would be to customize the surface treatment to achieve varied roughnesses across different areas of the implant. For instance, applying a higher roughness to specific regions could promote cell adhesion, while maintaining a smoother surface at the interface between the implant and adjacent bones could reduce friction and improve overall functionality.
Research suggests that antibiotic coatings are also critical for the integration of implants within the patient’s body [
59,
60]. Silver nanoparticles, used by Deng et al. [
61] as a coating agent on PEEK implant surfaces, were proven to prevent biofilm formation and limit immune reactions, while maintaining the mechanical properties of the coated implant. Alternatively, totarol, known for its strong antibacterial properties, was successfully applied to PEEK implants, leading to reduced immune response at the implant location [
62].
The simulation model produced satisfactory results in terms of strains and contact pressure for comparative purposes. Moreover, other studies have demonstrated similar and satisfactory results using analogous procedures. Shim et al. [
63] developed a hybrid method capable of generating patient-specific FE meshes from sparse or incomplete clinical datasets, though their focus was on a single bone rather than an articulation. Varghese et al. [
64] developed FE models based on CT scans that accurately determined strain and stress responses to two different loading conditions. The simulation model developed in this study incorporated four different types of movements combining bending and torsion. Validation of the model generation under more complex loading conditions will be pursued for greater clinical relevance.
However, it is important to note that certain damping effects, such as those from tendons, synovial fluid, blood vessels, or skin, were not considered in the current model for simplification reasons. While these complexities could influence the absolute output results, as highlighted by Viceconti et al. [
65], the comparison study remains valid, since the same simplifications were applied uniformly across all models, thereby damping them consistently [
54].
The linear material model employed may not accurately reflect real-world behavior, and was used for comparison purposes, although the calculated strain values remained below the ultimate strain. The PEEK implant was predicted to withstand 14 times the patient’s weight without failure. For those concerned with result accuracy, implementing a nonlinear material law could provide more precise stress and strain values, albeit at the expense of convergence stability and increased computational cost. Additionally, incorporating the non-linearity of large displacement options could enhance the result accuracy.
The friction coefficient, set at 0.05 based on the literature, did not undergo thorough estimation of its influence on results. This coefficient is influenced by various factors such as the age, sex, and health conditions of the patient [
66], making it difficult to determine accurately [
67]. Moreover, even with an accurate friction coefficient between the bones implemented in the simulation, the friction coefficient between the implant and the surrounding bones may differ, as highlighted by Rancourt et al. [
68]. Therefore, additional investigations should be conducted to examine the influence of the friction coefficient on the overall mechanical behavior of the ankle joint following the implementation of the implant.
The mechanical properties of the considered materials were also derived from the literature, but performing physical tensile and fatigue tests on the printed specimen would contribute to more accurate results and instill confidence in the simulation model.
Considering the long-term behavior of the printed model, particularly the adhesion between different layers of 3D-printed implants, is critical. Ongoing physical tests will be instrumental in further validating the simulation model [
59].