Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.10.30.685681

Chitosan-Polyphosphate Scaffold Loaded with Copper for Endodontic Regeneration: A Laboratory Study

Abstract

ObjectiveRegenerative endodontics procedures show promise in treating immature teeth with necrotic pulp and apical periodontitis. This procedure involves the replacement of damaged and infected pulp tissue with viable tissue that restores the normal tooth structure and function. Antimicrobials are currently used to control the infection; however, they are cytotoxic to stem cells of the apical papilla (SCAP) and can lead to root canal calcification. Management of these teeth requires a scaffold that can control root canal infection, wick the blood into the canal, and support the viability and differentiation of SCAP while inhibiting intracanal calcification. This study aims to develop a composite scaffold made of polyphosphate, a calcium binding inorganic polymer shown to promote cell proliferation and tissue regeneration, chitosan, a natural antimicrobial polymer that supports stem cell viability and activity, and copper, a metal ion with bactericidal properties. MethodologyThe scaffold was prepared by adding copper (Cu) to chitosan solution, followed by polyphosphate. The resulting scaffold was then freeze-dried and analyzed for elemental composition, chemical structure, release of Cu, antibacterial properties, cytotoxicity, as well as differentiation and mineralization assays. Data were analysed by a two-way analysis of variance (ANOVA) followed by the Tukey post hoc test. ResultThis study demonstrates that, by combining polyphosphate and chitosan, we could fabricate a scaffold that inhibits bacterial growth by 40 % and supports the viability of fibroblast and SCAP. Adding copper to this scaffold further increased bacterial growth inhibition by up to 68% while preserving cell viability. The immunocytochemistry and Alizarin Red staining revealed that this scaffold also supports the odontogenic differentiation of these stem cells while inhibiting their mineralization potential. Furthermore, this scaffold can be fabricated as a 3D cone-shaped scaffold with a strong vertical wicking ability at a rate of 0.5 mm/s and excellent degradability, with 53 % of the scaffold degraded after 28 days. ConclusionsThis study shows that a copper-loaded chitosan-polyphosphate scaffold combines biocompatibility, antibacterial activity, wicking ability, and biodegradability and has great potential as an endodontic regenerative scaffold.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Moussa, H., Mello, I., Leung, B. M., Filiaggi, M.. 2025-10-31. Chitosan-Polyphosphate Scaffold Loaded with Copper for Endodontic Regeneration: A Laboratory Study. https://doi.org/10.1101/2025.10.30.685681

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

KEEP EXPLORING

Related preprints

Comparative study of chlorophyll measurement in Physcomitrium patens moss using a conventional microscope adapted for combined 2D+1D imaging and spectral analysis

Imaging spectroscopy often requires expensive and complex equipment. Here we show a simple procedure for attaching a standard miniature fiber spectrometer to a conventional microscope, allowing easy integration of 2D imaging with 1D high-resolution spectral measurements. This combination provides much of the benefit of a full imaging spectrometer without the large equipment investment, and we provide instructions for modifying microscopes to this setup and the present measurements of living cells that demonstrate their performance. Using this setup, we compare the quantitative measurement of chlorophyll concentration in Physcomitrium patens moss using color imaging and spectral sampling.

bioengineering↗

De novo designed single-domain antibodies protect against lethal cobra venom neurotoxicity in vivo

Generative protein design can now rapidly produce de novo binders with high affinity and functional activity against a wide range of targets, including lethal snake venom toxins. However, so far most reported successes rely on new-to-nature scaffolds with limited therapeutic precedent. Single-domain antibodies (VHHs) offer a clinically validated alternative scaffold that can bind and neutralize long-chain -neurotoxins, which are some of the most lethal components in snake venoms. Here we compare three recently established de novo design models with VHH-design capabilities (Germinal, RFantibody, and BoltzGen) for their ability to generate VHHs against the neurotoxin -cobratoxin from the monocled cobra (Naja kaouthia). Using standardized model inputs and evaluation criteria based on AlphaFold3 interface confidence (ipTM) and RMSD self-consistency, we find that Germinal was the only method to generate designs passing stringent in silico criteria for experimental testing. We therefore performed a larger Germinal design campaign employing three different VHH frameworks and experimentally validated 46 designs in vitro. Of these, 42 expressed as soluble proteins and we identified four binding hits derived from two of the three tested frameworks. Of the four binders, two lead candidates were further characterized and demonstrated high affinity (KDs of 4.1 nM and 10.8 nM), monomeric behavior and low polyreactivity, indicating favorable biophysical and developability properties, as well as functional toxin neutralization in vitro. To assess their therapeutic potential we investigated their ability to protect against -cobratoxin toxicity in vivo. Both candidates fully protected mice after -cobratoxin challenge, with 100% survival compared to a lethal control. One candidate also retained notable neutralization capacity against whole venom of Naja kaouthia with a survival of 56%, while the other protected 22% when tested in a rescue setting. Together, we demonstrate that de novo VHH design can generate high affinity single-domain antibodies with in vivo protection against lethal cobra venom neurotoxicity, and provide practical insights into method- and framework-dependent performance.

bioengineering↗

Simple Feedback for Complex Movement: Capturing Whole-Limb Reorganization during Single-IMU Gait Retraining

Clinical gait retraining typically relies on multi-sensor arrays and high-dimensional feedback displays, imposing setup and interpretation burdens that limit routine clinical deployment. We developed a single-IMU visual biofeedback system that delivers real-time feedback of Lower Limb Trajectory Error (LLTE), a composite kinematic error metric integrating knee position and shank angle across the stance phase. Twenty able-bodied adults walked on a treadmill under two visual biofeedback targets (flexed-knee, extended-knee) while receiving either corrected (n=10) or uncorrected (n=8) feedback, where the correction accounted for limb orientation at initial contact. LLTE and stance-phase knee kinematics adapted consistently under the flexed-knee target for both feedback groups, with feedback formulation moderating the temporal trajectory of change. Adaptation toward the extended-knee target was limited, likely because participants were already operating near terminal knee extension and because the scalar error metric provided limited directional information for correction. Ankle range of motion (ROM) changed significantly across the stance phase under both target conditions, while hip ROM did not. Multiscale multivariate sample entropy (MSMVSE) increased monotonically with time scale across all conditions, with no statistically distinguishable difference between corrected and uncorrected feedback. These results suggest that single-IMU LLTE biofeedback can modify gait mechanics and that adaptation was expressed across multiple lower-limb segments rather than through changes at a single joint.

bioengineering↗