Search Results (1,656)

Sustainable nanotechnologies derived from renewable resources are increasingly being positioned at the interface of green chemistry, advanced drug delivery, and translational pharmaceutics. Over the past decade, lignocellulosic nanomaterials, chitin/chitosan platforms, polysaccharide-based nanogels and nano-enabled hydrogels, lignin- and polyphenol-derived nanostructures, and bio-based lipid nanocarriers have been engineered through progressively eco-efficient routes, including solvent-minimized self-assembly, nanoprecipitation, spray drying, hot-melt extrusion, and microfluidic-assisted fabrication. This work provides a structured evidence map of nano-enabled drug delivery and therapeutic platforms derived from renewable biological resources. Specifically, we aim to (i) identify and classify nanoplatform classes and renewable feedstocks; (ii) summarize reported pharmaceutical critical quality attributes (CQAs) and performance and safety endpoints; and (iii) appraise how “renewability” and “green” claims are evidenced (feedstock origin vs. process sustainability) and how frequently translational readiness factors (scalability, quality control, regulatory alignment) are addressed. We critically compare renewable and conventional nanomaterial platforms across key translational dimensions, including carbon footprint, batch consistency, biodegradability, functional tunability, safety/persistence, and scale-up maturity. Finally, we delineate a practical translational pathway—from biomass sourcing and fractionation to nanoformulation, characterization/stability, and GMP scale-up—highlighting cross-cutting enablers such as lifecycle assessment, EHS/toxicology risk assessment, quality-by-design, and regulatory alignment. Collectively, the evidence supports renewable nanomaterials as viable, scalable candidates for next-generation therapeutics, provided that variability control, standardized characterization, and safety-by-design principles are embedded early in development. Full article

In order to achieve rapid and qualitative detection of soluble heavy metal ions, nitrogen-doped fluorescent carbon quantum dots (N-CQDs) were synthesized using chitin extracted from shrimp and crab shells as the carbon source. The structural, morphological, and optical properties of the synthesized N-CQDs were systematically characterized using transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FTIR), Raman, X-ray photoelectron spectroscopies (XPS), ultraviolet-visible (UV-Vis) absorption spectroscopy and fluorescence spectroscopy. The resulting N-CQDs exhibited a carbonization yield of 54.46% and a fluorescence quantum yield of 34.33%. Their morphology, structure and optical properties were thoroughly characterized using a range of analytical techniques. The synthesized N-CQDs exhibited excellent fluorescence properties, and remarkable stability. When applied for metal ion detection, the N-CQDs displayed a distinct and selective fluorescence quenching response exclusively toward Fe³⁺ ions. The detection limit for Fe³⁺ at room temperature was 4.04 μmol/L. Furthermore, due to the inherent nitrogen present in the acetyl amino groups of chitin, nitrogen doping was achieved without the need for external dopants during the hydrothermal synthesis process. Owing to their high stability, low cost and low toxicity, the N-CQDs synthesized in this study provide a promising fluorescence sensing platform with excellent selectivity for Fe³⁺ detection, achieved through precise control of surface functional groups. Full article

The silkworm (Bombyx mori) is an economically important insect that plays a crucial role in agricultural development. Antimony tin oxide, a high-tech multifunctional nanomaterial, is extensively utilized in contemporary industries due to its properties of transparency, conductivity, and stability. Nevertheless, the toxicity and potential adverse effects of antimony tin oxide on living organisms remain poorly understood. In this study, we evaluated the effects of antimony tin oxide at varying concentrations (0–3.2 μg/μL) on the growth, oxidative stress response, gene expression, and midgut integrity of fifth-instar silkworm larvae. Exposure to high concentrations of antimony tin oxide resulted in a significant reduction in larval weight and severely disrupted the antioxidant defense system. RNA sequencing (RNA-Seq) analysis identified 239 differentially expressed genes (DEGs), which were confirmed by qPCR, revealing up-regulated lipid synthesis gene AGPAT5, down-regulated chitin degradation gene Chi, and suppressed glycerolipid hydrolysis gene H9J6N7_BOMMO. Histopathological and ultrastructural examinations revealed severe damage to the structure of midgut epithelial cells. Structural and functional analysis of conserved domains in key DEG-encoded proteins revealed that gene dysregulation disrupted energy metabolism and compromised the physical barrier, ultimately linking molecular abnormalities to observed tissue damage. These findings elucidate the mechanisms by which antimony tin oxide induces midgut toxicity through interference with critical metabolic pathways and functional perturbations at the molecular level. Full article

Lysin motif (LysM) domain-containing proteins are widespread in prokaryotes and eukaryotes, and play crucial roles in microbe-host interactions. In recent decades, a large number of LysM domain-containing proteins have been identified and confirmed to participate in various biological processes, including microbial growth, fungal pathogenesis, and recognition of pathogens by plant immune receptors. Emerging evidence has shown that some LysM domain-containing proteins in plant pathogenic fungi have evolved as key virulence factors. They manipulate host immune responses mainly by interfering with the plant’s perception of chitin, a core pathogen-associated molecular pattern (PAMP) of fungal cell walls. However, the functions of LysM domain-containing proteins in plant pathogenic fungi have not been systematically summarized. In this review, we discuss the latest advances in the structural characteristics, classification, and functional mechanisms of these proteins, as well as their applications in plant disease control. We also propose the current challenges and future research directions in this field. This review aims to deepen the understanding of the molecular mechanisms underlying plant-fungal interactions mediated by LysM domain-containing proteins and provide theoretical references for developing novel and environmentally friendly strategies for fungal disease management in agriculture. Full article

The tomato leaf miner, Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae), poses a significant threat to global tomato production. However, environmentally sustainable management strategies for this pest, as well as its mechanisms of insecticide resistance, remain insufficiently understood. Broflanilide, a novel meta-diamide compound, can bind specifically to the transmembrane domain of the RDL subunit, causing prolonged opening of the chloride channel, disruption of neurotransmission, and ultimately insect paralysis and death. This study employed the leaf immersion method to conduct bioassays on the second-instar larvae of T. absoluta to evaluate physiological responses to sublethal concentrations of the novel amide insecticide broflanilide. Subsequently, high-throughput transcriptome sequencing was performed to investigate changes in gene expression and metabolic pathways. Bioassay results determined the larval sublethal concentrations of broflanilide to be 0.136 mg/L (LC₁₀) and 0.210 mg/L (LC₃₀). Sublethal exposure significantly prolonged the larval period, reduced pupal weight, and inhibited fecundity of female adults. Transcriptomic and qPCR analyses revealed that, compared with the control (CK), expression of the vitellogenin gene Vg decreased by 15.99% and 30.27% under LC₁₀ and LC₃₀ treatments, respectively, while its receptor gene VgR decreased by 11.56% and 24.49%. Similarly, expression of chitin synthase genes chs1 and chs2 declined by 13.56% and 30.17% (chs1), and 7.85% and 19.45% (chs2), respectively. Gene expression analysis elucidated how sublethal insecticides treatment impact larval development and fecundity. Furthermore, the study revealed upregulation of cytochrome P450-mediated detoxification pathways and Toll/Imd immune signaling pathways under broflanilide stress, indicating activation of a coordinated defense response in T. absoluta. Sublethal broflanilide exposure modulated larval gene expression to balance growth, development, and stress adaptation. Such exposure exerts selective pressure on susceptible populations, potentially driving adaptive shifts in detoxification metabolism and contributing to the development of field resistance. These findings advance our understanding of the sublethal effects of novel insecticides and provide valuable insights for insecticide deployment strategies and resistance management. Full article

Marine byproducts generated from seafood processing represent valuable reservoirs of structurally and functionally distinct biomolecules, whose composition reflects species, habitat, and processing history. This systematic review identified which marine byproducts have been most extensively studied between 2020 and 2025, with emphasis on their composition, valorisation, and suitability for tracing their geographic origin. Following the PRISMA protocol, 6443 publications were initially retrieved, of which 96 peer-reviewed studies were included for data extraction and analysis. The five most frequently investigated byproducts—skin, bones, scales, shells, and roe—were identified as rich sources of proteins (collagen and gelatin), minerals (hydroxyapatite and calcium carbonate), polysaccharides (chitin), lipids (notably polyunsaturated fatty acids (PUFAs), docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA)), and vitamin B12. Collagen properties, particularly imino acid content, hydroxylation degree, crosslinking density, and thermal stability, correlate more strongly with environmental temperature than taxonomy, supporting their potential as markers for tracing geographic origin. The mineral fractions, dominated by hydroxyapatite in bones and scales, or calcium carbonate in shells, provided complementary inorganic fingerprints based on calcium-to-phosphorus ratios, carbonate substitution, trace element composition, and thermal analyses. While the lipid profile alone could not completely discriminate fish roe, proteomic techniques, such as MALDI-TOF MS, make it possible to reliably identify species. Collectively, these byproducts offer complementary organic and inorganic markers that support integrated strategies that allow tracing their origin and fostering their sustainable valorisation, overcoming a key technical bottleneck for their use. However, their large-scale conversion into market-ready products remains limited by technical complexity, process variability, and cost-related constraints. Full article

Acidic chitinase (Chia) degrades chitin, a structural polysaccharide in insect exoskeletons, and plays important roles in omnivorous and insectivorous mammals and birds. In birds, gene duplications have generated multiple Chia paralogs with functional divergence, but the molecular basis for this diversification remains unclear. Here, we characterized three chicken Chia paralogs (Chia1–3) and identified distinct pH-dependent enzymatic profiles. Chia1 is enzymatically inactive but was captured by chitin-affinity resin despite lacking a canonical chitin-binding domain, suggesting residual substrate interaction through the catalytic domain or a non-catalytic role. Chia2 exhibits maximal activity at pH 2.0, whereas Chia3 peaks at pH 5.0 and displays broader activity. Exon swapping and site-directed mutagenesis identified residues 104 (Ala in Chia2, Asp in Chia3) and 269 (His vs. Asn) as key contributors to pH-dependent activity differences. Reciprocal substitutions shifted pH profiles accordingly. Structural modeling and computational pKa predictions suggested that D213 and residue 269 may function as a pKa-regulating module influencing catalytic ionization. Comparative sequence analysis revealed lineage-specific conservation of these residues, consistent with adaptive divergence. Our findings show that limited amino acid substitutions can markedly modify pH-dependent enzymatic activity, providing mechanistic insight into how local residue variation contributes to the functional diversification of duplicated genes. Full article

The global demand for sustainable and effective food preservation techniques has spurred significant interest in biodegradable packaging materials, with chitosan films emerging as a promising solution for extending the shelf life of highly perishable seafood products such as shrimp. This review systematically summarizes recent advances in the development, characterization, and functional enhancement of chitosan-based films for shrimp. Chitosan, derived from chitin, has inherent antimicrobial, antioxidant, and biodegradable properties, making it an ideal candidate for eco-friendly packaging. The key physicochemical and functional properties of chitosan films, including their mechanical strength, barrier performance, and structural characteristics, are discussed. Functional enhancements, such as the incorporation of natural bioactive compounds (e.g., essential oils and plant extracts) and nanofillers, have been shown to significantly improve the antimicrobial efficacy, oxygen and water vapor barrier properties, and mechanical stability of films. A critical aspect of this progress is the synergistic effect achieved by combining chitosan with other antimicrobials, which broadens the spectrum of activity against various bacterial strains and enhances overall preservation efficacy. Recent studies have demonstrated that functionalized chitosan coatings effectively inhibit microbial growth, retard lipid oxidation, and maintain sensory and nutritional quality during refrigerated storage of shrimp. In addition, this review evaluates current limitations related to large-scale production, cost-effectiveness, and regulatory approval for commercial applications. Overall, chitosan-based preservation systems represent a promising approach for sustainable seafood packaging. Future research may focus on industrial scalability, multifunctional film design, and integration with smart/active packaging technologies. Full article

Postharvest Lentinula edodes (shiitake mushroom) undergoes rapid textural deterioration, which is primarily driven by complex cell wall remodeling. This study investigates the physiological and transcriptomic changes in L. edodes during storage at 4 °C for 8 days. Results showed that cellulose content significantly decreased, while chitin and β-glucan levels exhibited anomalous increases, accompanied by a surge in the activities of cellulase, chitinase, and β-1,3-glucanase. Concurrently, intensifying membrane lipid peroxidation and an imbalance in reactive oxygen species (ROS) homeostasis were observed. Transcriptomic analysis identified 2204 and 1808 differentially expressed genes (DEGs) at the middle (4 d) and late (8 d) storage stages, respectively. Partial Least Squares Regression (PLSR) identified a core module of nine key regulatory genes (VIP > 1.0), including β-glucanase, laccase, and catalase, which significantly contributed to the physiological shifts. The results suggest that an upstream ROS imbalance may contribute to the dysregulation of midstream laccases, potentially reducing the oxidative cross-linking of phenolic components and loosening the cell wall matrix. These alterations may increase the accessibility of structural polysaccharides to downstream cell wall-degrading enzymes, which could contribute to structural collapse, although functional validation is required to establish causality. These findings provide a gene-level framework for understanding postharvest edible fungi physiology. Full article

The molting of crustaceans is accompanied by exoskeleton reconstruction. To reveal the molecular regulation mechanism of exoskeleton remodeling, the transcriptomic profiles of the exoskeleton across the entire molting process in the red swamp crayfish Procambarus clarkii were investigated by RNA sequencing, yielding a total of 7671 differentially expressed genes (DEGs) across five different molting stages. Notably, the key DEGs were those related to cuticular exoskeleton synthesis (cuticular proteins), degradation (chitinase 2, chitinase 10) and hardening (chitin deacetylase 1), and their expression abundance varied by 10-fold or greater across the molting cycle. Analysis of Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) showed that significantly enriched pathways included the structural constituents of the cuticle, structural molecule activity, chitin binding of chitin metabolism, and hormone biosynthesis. The expression profiles of nine selected molting-related DEGs were further validated via real-time RT-PCR assays. The acquired unique temporal expression patterns involved in exoskeleton remodeling provide a preliminary insight into the regulation of gene expression during the molting cycle in the red swamp crayfish. Full article

The use of seven biomaterials was examined in the study: polyethylene (PE), polypropylene (PP), polyurethane (PU), teflon (PTFE), polycaprolactone (PCL), polylactide (PLLA), and a copolymer of poly L-lactide and dibutyryl chitin (PLLA/DBC). The use of these materials has not been discussed in the context of animal reproduction so far. Due to the specific nature of the reproductive system and the high sensitivity of reproductive cells, at the outset the biocompatibility and cytotoxicity of the materials were tested in somatic cell and embryo cultures. Additionally, the material properties of the catheters were determined in terms of the roughness of the internal and external surfaces, the stability of the shape of the catheters, their elasticity, durability, and ductility. Finally, clinical testing of the developed catheters was performed in laparoscopic transplantation of embryos into the uterine tubes of the sows. Significant toxicity of PTFE, PCL and PLLA/DBC towards the embryos was indicated in the cytotoxicity testing. In the materials testing, numerous flaws of the PP, PLLA, and PLLA/DBC catheters were indicated. In the final stage, catheters were developed using PE and PU. In clinical testing, these latter catheters exhibited high effectiveness in transferring embryos. Among the seven biomaterials tested, only polyethylene and polyurethane exhibited high biocompatibility and the material properties mentioned above. There is thus good indication for the introduction of these catheters for embryo transfer in animal reproduction biotechnology. Full article

Cuticular proteins (CPs)—key components of the insect exoskeleton—not only regulate development but also serve as structural barriers that enhance resistance against environmental stressors. This study identified CP gene families in Apis mellifera and analyzed their expression patterns during the worker capped brood development stages from mature larva to pre-eclosion. Using a comprehensive genome-wide bioinformatic approach, we identified 85 CP genes in A. mellifera which comprise six families: CPR (n = 43), CPAPs (n = 27), CPF (n = 2), Tweedle (n = 2), CPLCP (n = 8) and Apidermin (n = 3). Analysis of CP gene evolutionary relationship revealed that each CP family forms a distinct, relatively independent clade. Domain and motif analyses confirmed that all CPR members harbor a conserved Chitin_Bind_4 domain, consistent with CPR family structures in other taxa. Additionally, CPAP members possess one or three Chitin-binding Peritrophin-A domain (CBM_14), CPF members possess a conserved Pupal cuticle protein C1 domain (Cuticle_3), and Tweedle members contain a conserved domain of unknown function (DUF243). In addition, the analysis found no conserved domain within the CPLCP and Apidermin families. RNA-seq data revealed dynamic expression patterns of AmCPs during pupal development, with each gene family displaying a relatively characteristic temporal profile. Quantitative PCR validation of eight highly expressed CPR genes at 9 days post-capping confirmed the RNA-seq results. This work provides a comprehensive bioinformatic characterization and transcriptional analysis of CP genes in A. mellifera, offering a foundation for future functional studies on cuticle formation and identifying candidate genes potentially involved in cuticle development in honeybees. This work relies on transcriptomic data and in silico analyses. All proposed biological roles are hypothetical and require experimental validation. Full article

Postharvest autolysis severely compromises the commercial value of fresh Dictyophora rubrovolvata. This study integrated physiological, ultrastructural, and metabolomic analyses to elucidate the underlying mechanism. Results indicated a continuous decline in cellular adenosine triphosphate levels during storage, leading to an energy crisis and triggering cellular stress responses. Metabolomic analysis revealed that the fruiting bodies activate pathways such as glycolysis and the pentose phosphate pathway through metabolic reprogramming to maintain homeostasis. However, the intensifying energy crisis inhibited Calcium ion ATPase activity, disrupting ion homeostasis and leading to Ca²⁺ influx. This activated phospholipases and initiated membrane lipid degradation, accompanied by a burst of reactive oxygen species and elevated levels of H₂O₂ and malondialdehyde, creating a vicious cycle of oxidative stress. Concurrently, cell wall components (chitin, β-1,3-glucan, cellulose) are accelerated in degradation due to the upregulation of corresponding hydrolases. Transmission electron microscopy confirmed progressive disintegration of cellular structures, including mitochondria, the plasma membrane, and the cell wall. These findings establish an “energy-membrane lipid-cell wall” cascade framework, revealing that D. rubrovolvata autolysis is an active, orderly form of programmed cell death under energy stress. This study provides new insights into the physiological mechanisms of postharvest quality deterioration in edible fungi. Full article

Pyriproxyfen, a juvenile hormone analog insecticide, poses severe risks to non-target silkworms (Bombyx mori), as evidenced by disrupted metamorphosis—a process strictly dependent on chitin synthesis and its precursor trehalose. However, the specific molecular interference of pyriproxyfen in these metabolic pathways remains unclear. This study investigated the transcriptional response of silkworm midguts to pyriproxyfen using RNA-Seq and validated spatiotemporal gene expression via qRT-PCR. By integrating transcriptomic data with long-term spatiotemporal profiling, we revealed novel tissue-specific expression dynamics. RNA-Seq identified 2059 differentially expressed genes, primarily enriched in metabolic pathways. Spatiotemporal analysis revealed that most chitin- and trehalose-related genes generally exhibited a biphasic “suppression–compensation” trend (initial downregulation followed by upregulation). Notably, tissue-specific responses were evident, with ChsA being continuously suppressed in the middle silk gland, which may be associated with impaired sericin secretion, while showing abnormal upregulation in the posterior silk gland. Additionally, trehalose metabolism genes (Treh and Tret) paralleled the fluctuation of chitin genes, indicating systemic metabolic reprogramming. These results suggest that the toxicity of pyriproxyfen is associated with a decoupling of trehalose metabolism from chitin synthesis and the induction of tissue-specific metabolic disorders. The tissue-specific, long-term spatiotemporal profiling of chitin and trehalose genes presented in this study fills a critical knowledge gap. This study characterizes the transcriptional profile associated with pyriproxyfen toxicity and provides a robust molecular reference for assessing its environmental risks to beneficial insects. Full article

While Saccharomyces cerevisiae (baker’s yeast) offers a safe, non-animal source of chitin-glucan (CG), its potential as a functional cosmetic ingredient has been overshadowed by industrial sources like Aspergillus niger. This study advances the existing literature by establishing a critical structure–function relationship for CG micro/nano particles extracted via three physical disruption methods: ultrasonic bath, ultrasonic probe, and autoclaving. The obtained CG was systematically characterized by physicochemical and biological tests. A significant trade-off was identified: while autoclaving (40 min) resulted in lower mass yield compared to ultrasonication, it produced particles with the highest crystallinity, an enriched chitin/glucan ratio, and the smallest particle size (~70% of particles with mean diameter of 480 ± 33 nm). Structurally, these sub-micron particles demonstrated superior colloidal stability and a physical “barrier effect” for sustained hydration, outperforming the amorphous structures typically associated with mild extraction. The anti-wrinkle efficacy was validated through a specific “triad” mechanism: (1) the insoluble 3D network ensures prolonged water retention, (2) the particles exhibit robust free radical scavenging activity (~67%), and (3) most notably, the specific nano-structure significantly upregulated Collagen Type I-α1 expression in human dermal fibroblasts (HDF) and human skin fibroblasts (HSF), surpassing commercial chitin controls. These findings prove that the extraction-induced nano-structure, rather than mass yield, is the determinant factor for bioactivity, positioning S. cerevisiae CG as a high-performance, multi-target ingredient for anti-aging formulations. Full article