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Due to the uncertainty of trauma or infection, customized bone substitutes are often required in clinic. Meanwhile, excessive use of antibiotics may lead to drug resistance. Therefore, the design of anti-infection bone tissue engineering scaffold is of very important. In this study, porous titanium alloy bone tissue engineering scaffolds were designed and fabricated by 3D printing. TiO2 nanotubes were further constructed on the scaffolds through electrochemical anodic oxidation, achieving the drug loading and anti-infection functions. The micron-level bionic pores were fabricated by the 3D printing process, and the secondary nanoscale-level nanotubes were achieved through the anodic oxidation process. Thereafter, the micro–nano structured porous bone tissue engineering scaffolds are presented. This structure features that the drug release rate can be regulated by loading the anti-infection drug minocycline and coating them with poly(lactic-co-glycolic acid) (PLGA) in the nanotubes. According to the results, the micro–nano composite porous scaffold showed uniform and controllable micro–nano pores, it may load anti-infection drugs and shown anti-infection ability. In addition, the PLGA coating may delay the drug release and maintain a sustained anti-infection function for the scaffold in a week. This study provides new ideas for designing antibacterial bone tissue engineering scaffold.

The emergence of tissue engineering provides an alternative therapeutic strategy for various regeneration. It is the crucial step for choosing an ideal scaffold to support the cellular behaviors of various functional cells. Various biomaterials have been found or synthesized and applied to tissue repair. Among these biomaterials, as a natural-derived material, decellularized extracellular matrix (dECM) derived from cells, tissues, and organs is attracting more and more interest due to its good biocompatibility, biodegradability, and the ability to mimic a microenvironment similar to extracellular matrix. More and more researchers utilized dECM derived from cells, tissues, and organs to fabricate tissue-engineered scaffolds to repair musculoskeletal tissues, since the bioactive molecules of dECM, such as fibrous proteins, proteoglycans, and adhesive glycoproteins, could provide various bioactive cues for tissue regeneration and remodeling. The physiochemical properties of dECM can be enhanced by changing decellularization and modification techniques. In addition, dECM can act as carriers of drugs, factors, or exosomes, delivering agents to injured tissues and promoting tissue repair and regeneration. Therefore, we conduct this review to discuss the current status and challenges of dECM in repairing the musculoskeletal system. Furthermore, the fabrication and modification of dECM were also discussed in our study.

The bed structure of high-grade large-scale CNC machine tools is crucial for maintaining their long-term service accuracy. This study focused on the key casting process of large nodular cast iron beds. AnyCasting software was employed to simulate and analyze the casting scheme, and then the mold filling and solidification processes were proposed based on the simulation results. The proposed casting scheme indicates that the designed gating system exhibited excellent filling capability. The dual sprue ceramic pipe bottom pouring technique, in conjunction with the chills, not only improved casting efficiency but also met the requirements of sequential solidification design. The castings possessed a dense microstructure characterized by uniform and stable phase composition, primarily comprising lamellar pearlite, with ≤0.5% of phosphorus eutectic and cementite. Furthermore, the microstructure of these materials displayed favorable graphite morphology with a spheroidization rate exceeding 85% and spheroidization grade of 2–3. This study has important academic and application value for the casting process of producing low-stress, high-grade CNC machine tool bed cast iron materials.

Porous structures and surface morphology of bone tissue scaffolds play an important role in improving the biocompatibility and antibacterial properties for bone repair. In this study, we investigated the effect of different anodic oxidation parameters on the nanotubes morphology in 3D printed porous titanium scaffolds. Micron-scale pores were fabricated by 3D printing first, and then the nano-scale tubes were obtained via anodizing treatments. The results demonstrated that the morphology of the nanotubes depended on the anodic oxidation time and voltage, respectively. Longer anodic oxidation led to the formation of circle-like nanotubes, and the diameter of the nanotubes increased with the voltage. The scaffolds anodized at 30 V showed the best cell proliferation potential. The presence of nanotubes on the surface of scaffold altered the adhesion of bacteria so that it improved the antibacterial properties of scaffold. The formation of nanotubes improved the drug-loading ability of the scaffold, which are used for loading of minocycline antibacterial drugs. The proposed 3D printed porous Ti6Al4V scaffold with nanotubes surface modification showed obvious antibacterial effect, which is expected to have a promising application in antibacterial bone prosthesis.

Nano-hydroxyapatite (nano-HA) has been widely studied as a promising biomaterial because of its potential mechanical and biological properties. In this article, different synthesis methods for nano-HA were summarized. Key factors for the synthesis of nano-HA, including reactant concentration, effects of temperature, PH, additives, aging time, and sintering, were separately investigated. The biological performances of the nano-HA depend strongly on its structures, morphology, and crystallite sizes. Nano-HA with different morphologies may cause different biological effects, such as protein adsorption, cell viability and proliferation, angiogenesis, and vascularization. Recent research progress with respect to the biological functions of the nano-HA in some specific biological applications are summarized and the future development of nano-sized hydroxyapatite is prospected.

Three-dimensional (3D) printing technology has the advantages of fast design and fabrication in clinical orthopedics. This study proposed the application of 3D-printed personalized reverse shoulder prosthesis in a reverse total shoulder arthroplasty for a patient with tuberculosis of the shoulder joint. Traditional and personalized shoulder prostheses were compared and studied. The mechanical simulation analysis was conducted on the individualized prosthesis and scapula. A personalized reverse total shoulder prosthesis was fabricated by 3D printing technology. Finite element analyses were conducted for implantation of traditional and personalized prostheses. The numerical results show that the maximum equivalent stress of screws inserted into bone tissue is 43.23 MPa in the personalized prosthesis. But in traditional prostheses, the maximum equivalent stress of screws performing the same function is 246.50 MPa. The structural advantages of the personalized prosthesis effectively reduce the local pressure of the screws to ensure the safety and effectiveness of the material during service. At the same time, the scapula paired with the personalized prosthesis also shown a smaller mean equivalent stress that can reduce patient stress. The postoperative evaluation of implant stability and patient status was good. The results indicated that 3D printing technology has important application value in orthopedic surgery.

Extracellular vesicles (EVs), products released by cells in multiple biological activities, are currently widely accepted as functional particles and intercellular communicators. From the orthodox perspective, EVs derived from apoptotic cells (apoEVs) are responsible for cell debris clearance, while recent studies have demonstrated that apoEVs participate in tissue regeneration. However, the underlying mechanisms and particular functions in tissue regeneration promotion of apoEVs remain ambiguous. Some molecules active during apoptosis also function in tissue regeneration triggered by apoptosis, such as caspases. ApoEVs are generated in the process of apoptosis, carrying cell contents to manifest biological effects and possess biomarkers to target phagocytes. The regenerative effect of apoEVs might be due to their abilities to facilitate cell proliferation and regulate inflammation. Such regenerative effect has been observed in various tissues, including skin, bone, cardiovascular system, and kidneys. Engineered apoEVs are produced to amplify the biological benefits of apoEVs, rendering them optional for drug delivery. Meanwhile, challenges exist in thorough mechanistic exploration and standardization of production. In this review, we discussed the link between apoptosis and regeneration, current comprehension of the origination and investigation strategies of apoEVs, and mechanisms in tissue regeneration of apoEVs and their applications. Challenges and prospects are also addressed here.