bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.09.05.673512

2D Boron Nanoplatelets as a Multifunctional Additive for Osteogenic, Gram-Negative Anti-Microbial and Mechanically Reinforcing Bone Repair Scaffolds

Abstract

Two-dimensional boron offers unique advantages in bone tissue engineering, unlocking capabilities that conventional additives struggle to achieve. In this study, we leverage the 2D morphology and intrinsic bioactivity of boron nanoplatelets, incorporated into collagen-based scaffolds, to simultaneously achieve osteogenic, neurogenic, angiogenic, anti-inflammatory, mechanically reinforcing, and anti-microbial effects. We synthesize boron nanoplatelets from non- layered precursors using liquid-phase exfoliation and combine them with collagen to form boron- collagen scaffolds (BColl). Boron significantly reinforces the collagen matrix, beneficial for mechanoresponsive bone cells. Osteoblasts and mesenchymal stem cells exhibit healthy morphology and proliferation on BColl films and scaffolds, with extended culture leading to increased alkaline phosphatase release and significantly increased calcium deposition, indicating enhanced osteogenesis. E. coli viability decreases significantly on BColl films, demonstrating their potential to limit post-implantation infections. Finally, we observe angiogenic, neurogenic and anti-inflammatory effects, with dose-dependent upregulation of vascular endothelial growth factor-A, nerve growth factor-beta and interleukin-10, and downregulation of interleukin-6 highlighting borons potential to drive pro-reparative processes. Taken together, these data showcase borons potential in developing next-generation bone biomaterials, by offering multifunctional benefits to clinically relevant aspects of bone regeneration such as mineralization, angiogenesis, and innervation, while improving the mechanical and anti-microbial properties of natural polymer scaffolds. Graphical Abstract & ToC TextAn ideal bone scaffold would enhance osteogenesis, angiogenesis, and neurogenesis, while preventing inflammation, infection, and stiffness mismatch. 2D materials unlock diverse properties arising from the nanoplatelet morphology, while simultaneously leveraging the intrinsic properties of the material, enabling such multifunctional scaffolds. In this study, we combine 2D boron nanoplatelets with a bioactive collagen matrix to form a multifunctional, versatile bone repair scaffold with osteogenic, angiogenic, neurogenic, anti-inflammatory, and anti-microbial behaviour. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=175 SRC="FIGDIR/small/673512v1_ufig1.gif" ALT="Figure 1"> View larger version (68K): org.highwire.dtl.DTLVardef@1611344org.highwire.dtl.DTLVardef@37f0bcorg.highwire.dtl.DTLVardef@9e044dorg.highwire.dtl.DTLVardef@2c6bf5_HPS_FORMAT_FIGEXP M_FIG C_FIG

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Maughan, J., Kaur, H., Prendeville, L., Carey, T., O'Connor, C., Synnatschke, K., Palomeque, J. C., Woods, I., O'Brien, F. J., Coleman, J. N.. 2025-09-10. 2D Boron Nanoplatelets as a Multifunctional Additive for Osteogenic, Gram-Negative Anti-Microbial and Mechanically Reinforcing Bone Repair Scaffolds. https://doi.org/10.1101/2025.09.05.673512

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Single-Component Photo-Crosslinked Lipoic Acid Functionalized Mucin Hydrogels: Dynamic Mucus Mimetics for Antiviral Protection

Native mucus protects epithelial surfaces through viscoelastic networks of disulfide-linked mucins. However, commercially available mucins often fail to reconstitute comparable mechanical and barrier properties, while synthetic and hybrid mucus mimetics require polymeric crosslinkers that may alter mucus-like composition. Inspired by the native architecture, we directly functionalized porcine gastric and bovine submaxillary mucins with -lipoic acid to develop a single-component, photo-crosslinkable hydrogels. Upon UV irradiation (365 nm), the modified mucins rapidly form disulfide-crosslinked networks without added photo-initiator/ polymeric crosslinkers, two orders of magnitude faster as compared with PEG-SH approaches. The resulting mucin-lipoic acid (MUC-LA) hydrogels exhibit mucus-relevant properties, including tunable viscoelasticity, redox responsiveness, self-healing, and size-dependent restrictions on nanoparticle transport. In transwell-based infection models, MUC-LA hydrogels (2-3%) mimicking the healthy airway mucus (G' {approx} 10-20 Pa) suppress epithelial infection by SARS-CoV-2 and influenza A virus. Crosslinked MUC-LA provides greater protection against SARS-CoV-2 than the non-crosslinked, whereas both formulations suppress influenza A infection, suggesting distinct contributions from network formation and mucin-associated interactions. These findings establish a dynamic, mucus-mimetic platform integrating rapid photo-gelation, controllable mechanics, selective transport, and antiviral barrier functionality. MUC-LA hydrogels offer opportunities to investigate mucosal transport and host-pathogen interactions, with potential applications in drug delivery, and as biomaterials.

bioengineering↗

A Fibrous Optofluidic Probe for Endovascular Sensing of Blood Oxygenation and Flow Velocity

Local hemodynamic information including blood oxygenation and flow velocity could guide vascular interventions, yet obtaining these parameters in deep, narrow vessels remains challenging. Here, we report a flexible, submillimeter-scale fibrous optofluidic probe for endovascular sensing of blood oxygenation and flow velocity. The probe integrates a polymer optical fiber for light transmission with a microfluidic tube for dye injection, enabling spectroscopic oximetry and fluorescence dilution-based velocimetry through a single device. Via vascular intervention, we demonstrate local hemodynamic sensing in rabbit arteries and angiography-guided deployment in canine carotid arteries. The probe captures local changes in blood oxygenation and flow velocity during vascular occlusion and reperfusion, revealing hemodynamic disturbances that are not reflected in peripheral monitors. These results illustrate the complementary information provided by local oximetry and velocimetry and establish a compact optofluidic platform for quantitative hemodynamic monitoring during vascular interventions.

bioengineering↗

Broad-spectrum in situ genetic reprogramming of native microbiomes

Complex microbial communities are found throughout terrestrial, aquatic, and animal-associated ecosystems. Genetic modification of discrete microbial taxa within native communities represents a powerful tool to study and augment microbiome functions. Herein, we develop Synthetic Phage Assisted Reprogrammable and Targetable Addition (SPARTA) as a one-step strategy for packaging, delivering, and integrating large synthetic DNA into a broad range of native microbiomes. SPARTA leverages a broad-spectrum synthetic phage particle for in situ genome engineering within complex soil, freshwater, and mammalian fecal microbiomes, reprogramming 59 native species across 16 families. By modulating SPARTA components, we further demonstrated tunability of SPARTA towards targeted microbiome population. Additionally, we built a novel companion tool to quantitatively identify engineered taxa, named 16S crRNA-guided inference of bacterial engineering sequencing or ScRibe-seq. The SPARTA-ScRibe-seq pipeline delivered and validated functional synthetic gene clusters in diverse native microbiomes while preserving the original microbial community structure. Together, this novel genome engineering framework constitutes an end-to-end programmable platform for rational and customizable reprogramming of native microbiomes.

bioengineering↗