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Each year, more than four million people around the world undergo bone grafts and prosthesis transplants to treat bone defects and injuries by repairing and/or replacing native bone. As a result, the scaffold holds great promise for the regeneration of damaged or diseased bone tissues. One of the key components is the design of scaffolds that can mimic the structure and function of natural bone. Based on unit cell design, triply periodic minimal surface (TPMS) has attracted the attention of researchers for designing porous scaffolds. In current study, uniform and multi-morphology hybrid graded structures were designed based on TPMS, namely, primitive and I-graph-wrapped package (IWP) minimal surfaces. Furthermore, a computational fluid dynamic (CFD) model was designed based on COMSOL Multiphysics to understand the fluidic characteristics (permeability and wall shear stress) of the structures. The results show that structures reported a permeability of 7.4 – 14.3 × 10 -8 m2, meeting the requirements of natural bone. Moreover, the average wall shear stress of 0.5 – 136 mPa was observed, suitable for osteoblast differentiation and proliferation.

Acetabular cup liners made of ultra‐high molecular weight polyethylene (UHMWPE), in hip implants fail mostly due to wear debris generation and poor wear resistance. Consequently, strengthening UHMWPE becomes essential. The current work exhibits how the addition of 5 vol% carbon nanotubes (CNT) and functionalized carbon nanotubes (fCNT) in UHMWPE (denoted as U) affects the mechanical properties (hardness, elastic modulus) and tribological properties (wear resistance) of biocomposites. To form a composite, powders were mixed using a planetary centrifugal mixer followed by freeze‐drying to disperse‐CNTs, followed by its compression molding at 220°C for 1 h at 10 MPa. With the addition of CNT and fCNT, ≥95% densification was obtained for all samples resulting an increase in hardness and elastic modulus from 74.96 MPa to 168.11 MPa (124%) and 1.65 GPa to 2.96 GPa (79%), respectively, which led to the reduction in wear rate from 12.5 × 10−5 mm3/Nm (U) to 2.5 × 10−5 mm3/Nm (UfCNT). The amount of apatite formation enhanced from U (58.2%) to UfCNT (65.1%) is confirmed via X‐ray diffraction and X‐ray photoelectron spectroscopy. Cell proliferation studies have validated the cytocompatible efficacy of U‐CNT composites with osteoblast‐like MG‐63 cells, making UfCNT as potential material for acetabular cup liners. [ABSTRACT FROM AUTHOR]

Antimicrobial potential of bioactive glass (BAG) makes it promising for implant applications, specifically overcoming the toxicity concerns associated with traditional antibacterial nanoparticles. The 58S composition of BAG (with high Ca and absence of Na) has been known to exhibit excellent bioactivity and antibacterial behaviour, but the mechanisms behind have not been investigated in detail. In this pioneering study, we are using Atomic Force Microscopy (AFM) to gain insights into 58S BAG's adhesive interactions with planktonic cells of both gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli) bacteria; along with the impact of crystallinity on antibacterial properties. We have recorded greater bacterial inhibition by amorphous BAG compared to semi-crystalline glass–ceramics and stronger effect against gram-negative bacteria via conventional long-term antibacterial tests. AFM force distance curves has illustrated substantial bonding between bacteria and BAG within the initial one second (observed at a gap of 250 ms) of contact, with multiple binding events. Further, stronger adhesion of BAG with E.coli (~ 6 nN) compared to S. aureus (~ 3 nN) has been found which can be attributed to more adhesive nano-domains (size effect) distributed uniformly on E.coli surface. This study has revealed direct evidence of impact of contact time and 58S BAG's crystalline phase on bacterial adhesion and antimicrobial behaviour. Current study has successfully demonstrated the mode and mechanisms of initial bacterial adhesion with 58S BAG. The outcome can pave the way towards improving the designing of implant surfaces for a range of biomedical applications. [ABSTRACT FROM AUTHOR]