Skin tissue engineering scaffolds should possess key properties such as porosity, degradability, durability, and biocompatibility to effectively facilitate skin cell adhesion and growth. In this study, recombinant human collagen (RHC) was used to fabricate porous scaffolds via freeze-drying, offering an alternative to animal-derived collagen where bovine collagen (BC)-based scaffolds were also prepared for comparison. The internal morphology of the RHC scaffolds were characterized by scanning electron microscopy (SEM) and the pore size ranged from 68.39 to 117.52 µm. The results from compression and fatigue tests showed that the mechanical strength and durability of RHC scaffolds could be tailored by adjusting the RHC concentration, and the maximum compressive modulus reached to 0.003 MPa, which is comparable to that of BC scaffolds. The degradation test illustrated that the RHC scaffolds had a slower degradation rate compared to BC scaffolds. Finally, the biocompatibilities of the porous scaffolds were studied by seeding and culturing the human foreskin fibroblasts (HFFs) and human umbilical vein endothelial cells (HUVECs) in samples. The fluorescent images and Cell Counting Kit-8 (CCK-8) assay revealed RHC porous scaffolds were non-cytotoxic and supported the attachment as well as the proliferation of the seeded cells. Overall, the results demonstrated that RHC-based scaffolds exhibited adequate mechanical strength, ideal biodegradability, and exceptional biocompatibility, making them highly suitable for skin-tissue-engineering applications.

Lumbar interbody fusion (LIF) is a standard treatment for spinal instability, yet postoperative subsidence and adjacent segment degeneration (ASD) remain critical challenges. This study evaluates the biomechanical efficacy of personalized porous fusion cages—featuring Gyroid (G-Cage) and Voronoi (V-Cage) architectures—against classic (C-Cage) and personalized (P-Cage) designs, aiming to enhance stability and mitigate subsidence risks. A finite element model of the L3–L4 segment, derived from CT scans of a healthy male volunteer, was developed to simulate six motion modes (compression, rotation, flexion, extension, and left/right bending). Biomechanical parameters, including range of motion (ROM), cage stress, endplate stress, and displacement, were analyzed. The results demonstrated that the V-Cage exhibited superior performance, reducing ROM by 51% in extension, cage stress by 41.7% in compression, and endplate stress by 63.7% in right bending compared to the C-Cage. The porous designs (G-Cage, V-Cage) exhibited biomimetic stress distribution and minimized micromotion, which was attributed to their trabecular-like architectures. These findings highlight the Voronoi-based porous cage as a biomechanically optimized solution, offering enhanced stability and reduced subsidence risk when compared to classic implants. The study underscores the potential of patient-specific porous designs in advancing LIF outcomes, warranting further clinical validation to translate computational insights into practical applications.

Rapid corrosion and poor coating adhesion continue to limit the use of magnesium alloys as temporary orthopedic implants. The two-stage laser process was developed to separate the high-temperature melting of 45S5 bioactive glass (BG) from the low-melting-point AZ31 substrate. Femtosecond-laser grids with spacings of 100, 200, and 300 μm were first produced on AZ31 to provide anchoring sites. Then, the target 45S5 BG was suspended above the substrate, locally melted with CO₂ laser, and transported onto the textured surface by gas jet. The 200 μm grid texture for Mg substrate with lowest water contact angle could give the highest tape-test adhesion rating (4B). At the selected deposition conditions of 20 W and 20 L·min⁻¹, two coating cycles produced a continuous layer approximately 50.5 μm thick. Relative to bare Mg alloy, this double-layer coating increased polarization resistance from 1.20 × 103 to 1.39 × 10⁵ Ω·cm² and decreased corrosion current density from 8.70 × 10⁻⁴ to 5.33 × 10⁻⁶ A·cm⁻². It also limited alkalization and mass loss during 28 days in simulated body fluid. As such, the double-layer surface coating supported apatite formation and improved MC3T3-E1 proliferation and alkaline phosphatase activity. These findings indicated that suspended-target deposition was able to form adherent, bioactive glass coatings on magnesium while limiting direct thermal damage to the substrate.