Search bioRxiv⌕ Search

bioRxiv · 10.1101/2024.05.03.592363

Tuning of Chitosan with Lignin derived Bioactive Properties to develop a Lignin Reinforced and Sustainable Food Packaging Biomaterial

Abstract

The crucial component of food storage, preservation, and transportation is food packaging. Biodegradable biopolymers are a major area of focus for the future development of food packaging materials due to their ability to mitigate adverse environmental impact by reducing plastic pollution and promoting sustainable waste management practices. Exploring renewable resources is crucial for facilitating the transition from non-renewable practices to sustainability. Chitosan is known for its superior film-forming abilities but has limited antibacterial activity. The inherent properties of lignin, including its high tensile strength, antioxidant, antimicrobial, and UV barrier ability, can contribute to enhance chitosan film performance when added as a co-polymer, making it an active material for food packaging applications. The present work explores the acid-alkali treatment to extract lignin from sugarcane tops, an abundant agricultural waste, and the application of extracted lignin in biopolymer-based hydrogel synthesis for food packaging. The goal is to enhance the hydrogel formulation by incorporation and optimisation of lignin that holds high antioxidant, antimicrobial, UV barrier, and mechanical properties along with significantly low water transmissibility. This study introduces a novel approach by utilizing lignin extracted from sugarcane tops (SCT) rather than commercially derived lignin, thereby expanding the raw material scope of lignin applications. The incorporation of higher proportions of lignin in the hydrogel formulations represents an advancement over reported studies, aimed at improving the bioactivity of the hydrogel by leveraging its advantageous characteristics emanating from lignin. This approach can also reduce the dependency on chitosan which is relatively expensive. Further, the modified synthesis of hydrogels expedited through heating method contributes to shorten the time duration needed for hydrogel film casting and drying. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=139 SRC="FIGDIR/small/592363v1_ufig1.gif" ALT="Figure 1"> View larger version (48K): org.highwire.dtl.DTLVardef@c88b2forg.highwire.dtl.DTLVardef@29c658org.highwire.dtl.DTLVardef@9ce06borg.highwire.dtl.DTLVardef@151a8b5_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIEnhanced lignin extraction from sugarcane tops using Plackett Burman Design C_LIO_LIFormulating green packaging hydrogels through valorisation of sugarcane tops C_LIO_LIHeating-based short time casting method for Lignin/Chitosan hydrogel synthesis C_LIO_LIOptimization of lignin content in the hydrogels for balanced mechanical and bioactive properties C_LI

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Garg, S., Althuri, A.. 2024-05-05. Tuning of Chitosan with Lignin derived Bioactive Properties to develop a Lignin Reinforced and Sustainable Food Packaging Biomaterial. https://doi.org/10.1101/2024.05.03.592363

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↗