Cross-linking Sites Research Articles

Amplifying endogenous stem cell migration for in situ bone tissue formation: Substance P analog and BMP mimetic peptide-loaded click-crosslinked hyaluronic acid hydrogel

Endogenous stem cell-driven in situ bone tissue formation has recently garnered increasing attention. Therefore, our study sought to refine methods to enhance the migration and subsequent osteogenic differentiation of these cells. Our innovative approach involves using an injectable hydrogel that combines click cross-linking sites and a BMP-2 mimetic peptide (BP) with hyaluronic acid (HA). This injectable formulation, hereinafter referred to as SPa + Cx-HA-BP, incorporates a substance P analog peptide (SPa) with Cx-HA-BP, proving versatile for in vitro and in vivo applications without cytotoxicity. The controlled release of SPa creates a gradient that guides endogenous stem cells towards the Cx-HA scaffold from specific tissue niches. Both Cx-HA and SPa+Cx-HA induced minimal changes in the expression of genes associated with osteogenic differentiation. In contrast, these genes were robustly induced by both SPa + Cx-HA+BP and SPa + Cx-HA-BP, in which BP was respectively integrated via physical and chemical methods. Remarkably, chemically incorporating BP (Cx-HA-BP) resulted in 4–9 times higher osteogenic gene expression than physically mixed BP in Cx-HA+BP. This study validates the role of SPa role in guiding endogenous stem cells toward the hydrogel and underscores the substantial impact of sustained BP presence within the hydrogel. Collectively, our findings offer valuable insights for the development of innovative strategies to promote endogenous stem cell-based tissue regeneration. The developed hydrogel effectively guides stem cells from their natural locations and facilitates sustained osteogenic differentiation, thus holding great promise for applications in regenerative medicine.

The crosslinking sites and molecular conformation of gelatin hydrogel modified by transglutaminase

This work aimed to investigate the covalent crosslinking sites induced by transglutaminase (TGase, EC 2.3.2.13) in gelatin hydrogel and their impact on the gelatin molecular conformation. LC-MS/MS results demonstrated that Lys644 and Gln1351 of α1 chain and Gln19 of α2 chain were the main sites. The results of molecular dynamic (MD) simulation indicated that at the moderate degree of covalent crosslinking (13.55%), Radius of gyration (Rg) values decreased from 11.5 to 10.0 nm at 4 °C and led to a more compact structure, therefore enhancing structural tightness and gel strength. As the degree of crosslinking rose, the number of crosslinking sites gradually increased, with a predominant distribution in the C-terminal pro-peptide of gelatin chain. At the high crosslinking degree (37.48%), Rg value decreased at 100 °C and gelatin chains were connected through a “head to tail” linkage configuration, resulting in a significant reduction in the triple helix-like structure. The structure maintained the gel-forming ability at high temperature while lowering the aggregation energy of water molecules from −2.359 × 105 to −2.455 × 105 kJ/mol, leading to thermal irreversibility of gelatin hydrogel.

Effect of tremella polysaccharides on the quality of collagen jelly: insight into the improvement of the gel properties and the antioxidant activity of yak skin gelatin.

The present study aimed to investigate the effects of tremella polysaccharides on the gel properties and antioxidant activity of yak skin gelatin with a view to improving the quality of collagen jellies. The preparation of composite gels were performed by yak skin gelatin (66.7 mg mL-1) and tremella polysaccharides with different concentrations (0, 2, 4, 6, 8 mg mL-1), and finally the collagen jelly was prepared by composite gel (yak skin gelatin: 66.7 mg mL-1; tremella polysaccharides:6 mg mL-1) with the best performance. Tremella polysaccharides not only improved the hardness, springiness, gel strength, water holding capacity and melting temperature of yak skin gelatin, but also enhanced the composite gel's scavenging activity against ABTS radicals, DPPH radicals, O2 and OH radicals. The filling of tremella polysaccharides into the gelatin network increased the number of crosslinking sites inside the gel, which resulted in the gel network structure becoming dense and orderly. The gel particles became finer and more uniform, and the thermal stability was improved. Furthermore, the sensory score of commercially available gelatin jelly decreased more rapidly during storage compared to the composite gel jelly. The gel properties and antioxidant activity of yak skin gelatin were improved by adding tremella polysaccharides, and then the quality and storage properties of the jelly were improved, which also provided technical reference for the development of functional gel food. © 2024 Society of Chemical Industry.

Co-pyrolysis behaviors of biomass and polymer plastics by using reactive molecular dynamics simulation

Co-pyrolysis of oxygen-rich biomass and hydrogen-rich plastic polymer is a promising approach for waste management, which has been investigated by using reactive molecular dynamics simulation (ReaxFF MD) in this work. The blend models containing multicomponent mixtures of polymer (polyethylene, polypropylene, polystyrene) and biomass (cellulose, hemicellulose and lignin) were constructed for the first time, which is close to the real utilization of waste materials. The simulation results show that the degree of positive synergistic effect between biomass and polymer increases with temperature, where the polymer promotes biomass pyrolysis and delays its recombination. Co-pyrolysis greatly affects the product yields through cross reactions of hydrogen and hydroxyl transfer, leading to more oxygen-containing bio-oils produced with the aid of polymers providing hydrogen. Produced from heavy tar at first and light char at late pyrolysis period, char precursors are generated more and faster in the co-pyrolysis system with more biomass because oxygen functional groups provide the initial cross-linking sites. As compared to pyrolysis of only binary components, the observed qualitative synergistic results in co-pyrolysis of biomass-polymer mixtures provide important insights into the detailed reactions for co-pyrolysis process, which can complement experimental observations to modulate the nature and yield of the desired bio-oils and bio-chars.

Injectable nanoparticle-crosslinked xyloglucan/ε-poly-l-lysine composite hydrogel with hemostatic, antimicrobial, and angiogenic properties for infected wound healing

Skin wounds are susceptible to infection, leading to severe inflammatory reactions that can progress to chronic wounds, ultimately causing significant physical and mental distress to the patient. In this study, we propose an injectable composite hydrogel achieved through one-pot gelation of oxidized xyloglucan (OXG), cationic polyamide ε-poly-l-lysine (EPL), and surface amino-rich silicon nanoparticles (SiNPs). OXG exhibits commendable anti-inflammatory properties and provides crosslinking sites. SiNPs serve as mechanically reinforced crosslinkers, facilitating the construction of a dynamic Schiff base network. SiNPs significantly reduced the gelation time to 3 s and tripled the storage modulus of the hydrogels. Additionally, the combination of EPL and SiNPs demonstrated synergistic antimicrobial activity against both S. aureus and E. coli. Notably, the hydrogel effectively halted liver bleeding within 30 s. The hydrogel demonstrated outstanding shear-thinning and self-healing properties, crucial considerations for the design of injectable hydrogels. Furthermore, its efficacy was evaluated as a wound dressing in a mouse model with S. aureus infection. The results indicated that, compared to commercial products, the hydrogel exhibited a shorter wound healing time, decreased inflammation, thinner epithelium, increased hair follicles, enhanced neovascularization, and more substantial collagen deposition. These findings strongly suggest the promising potential of the proposed hydrogel as an effective wound dressing for the treatment of infected wounds.

Investigating Texture and Freeze-Thaw Stability of Cold-Set Gel Prepared by Soy Protein Isolate and Carrageenan Compounding.

In this study, the purpose was to investigate the effects with different concentrations of carrageenan (CG, 0-0.30%) on the gel properties and freeze-thaw stability of soy protein isolate (SPI, 8%) cold-set gels. LF-NMR, MRI, and rheology revealed that CG promoted the formation of SPI-CG cold-set gel dense three-dimensional network structures and increased gel network cross-linking sites. As visually demonstrated by microstructure observations, CG contributed to the formation of stable SPI-CG cold-set gels with uniform and compact network structures. The dense gel network formation was caused when the proportion of disulfide bonds in the intermolecular interaction of SPI-CG cold-set gels increased, and the particle size and zeta potential of SPI-CG aggregates increased. SG20 (0.20% CG) had the densest gel network in all samples. It effectively hindered the migration and flow of water, which decreased the damage of freezing to the gel network. Therefore, SG20 exhibited excellent gel strength, water holding capacity, freeze-thaw stability, and steaming stability. This was beneficial for the gel having a good quality after freeze-thaw, which provided a valuable reference for the development of freeze-thaw-resistant SPI cold-set gel products.

A polypyrrole-dopamine/poly(vinyl alcohol) anisotropic hydrogel for strain sensor and bioelectrodes

Flexible hydrogel-based wearable sensors are of interest for monitoring human movement and electrophysiological signal detection. The high mechanical properties, high conductivity, and sensing sensitivity are the main performance parameters. Inspired by the structure of human muscles, ligaments, and other tissues, a polypyrrole-dopamine/poly(vinyl alcohol) (DA-PPy/PVA) hydrogel with a bionic anisotropic structure is prepared in this study using a directed freeze–thaw strategy. The introduction of DA-PPy nanoparticles can significantly improve the mechanics, adhesion, and conductivity due to the high water dispersibility. Moreover, they can act as physical cross-linking sites to further improve the mechanical properties. The anisotropic structure would influence many properties (mechanical, conductivity, resistance to crack extension, etc.) of DA-PPy/PVA hydrogel. In addition, the prepared DA-PPy/PVA hydrogel exhibits a wide range of strain responses, moreover, its relative resistance change (ΔR/R0) strain curve maintains a line linear within 400% strain. The oriented structure would influence the sensing sensitivity, the gauge factor of anisotropic DA-PPy/PVA in parallel direction is 3.00. In addition, the anisotropic DA-PPy/PVA can effectively motor the physiological electrical signals as a bioelectrode. For example, the acquired electrocardiogram (ECG) and electromyography (EMG) signals not only are clearer than those of the commercial electrodes but show a higher signal-to-noise ratio. It is conceivable that the bionic anisotropic DA-PPy/PVA hydrogels provide a feasible material to construct flexible wearable sensors for monitoring human movement and electrophysiological signals.

Effect of Repeat Unit’s Composition Ratio on the Properties of a Random Copolymer: A Molecular Dynamics Simulation Study

For thermosetting resins the degree of cross-linking plays a crucial role in the dielectric properties of the resin. In our previous works we confirmed this by simulating the relationship between the dielectric properties of poly(2-(4-benzocyclobutenyl)-divinylbenzene (DVB-S-BCB)) and the degree of cross-linking. In our research described here, we constructed a novel random copolymer with all-hydrocarbon structure based on poly(DVB-S-BCB) by introducing styrene (St) as the second polymerization monomer, thus controlling the number of cross-linking sites in the polymer. The effect of changes in St monomer content (number of cross-linking points) in the polymer chains, i.e. DVB-S-BCB and St, on the dielectric properties of the cured resins was investigated by molecular dynamics simulations. The simulation results showed that increasing the St monomer content in the copolymer, decreasing the cross-linking points, led to an increase in the dielectric constant of the cured resin, in addition to which the copolymer exhibited excellent thermo-mechanical properties. We also tested resin samples prepared by the experimental method and compared them with the simulated data, confirming the reliability of the results within acceptable error limits.

Biomass crosslinked fluorinated methacrylate elastomer for stress sensors with recyclability, reprocessability, remoldability, and hydrophobicity

Fluorinated copolymers typically exhibit exceptional chemical inertness and interesting surface properties. However, the failure to further enhance the mechanical properties of copolymers, particularly their elasticity and resilience, is a significant constraint on their practical application due to the lack of cross-link sites. Here, we synthesize a series of fluorinated copolymers containing various contents of the aldehyde group via ternary emulsion copolymerization. Then, fluorinated elastomers are prepared by forming an imine-based network with a crosslinker. As a result, the tensile strength of the material is adjustable from 2.12 MPa to 9.26 MPa, while the water contact angle is adjustable from 91.3° to 112.6°, which greatly expands the scope of application of fluorinated material. On the other hand, the imine-based network established performs as a biomass dynamic cross-link network, and the dynamic nature of materials is studied. The elastomer is verified as a reprocessing, remoldable, and recyclable material, which meets the current idea of sustainable development. After the introduction of an ionic conducting liquid, the potential application of the ionic conducting elastomer in sensing is demonstrated through stress sensing testing. This functionalized fluorinated elastomers, which can be easily prepared by cross-linking, are important for promoting the development of fluorinated elastic materials.

Site‐Selective Photo‐Crosslinking of Stilbene Pairs in a DNA Duplex Mediated by Ruthenium Photocatalyst

AbstractWe herein report a method for site‐selective photo‐crosslinking of a DNA duplex. A stilbene pair was introduced into a DNA duplex and a ruthenium complex was conjugated with a triplex‐forming oligonucleotide. We demonstrated that [2+2] photocycloaddition of the stilbene pair occurred upon irradiation with visible light when the ruthenium complex was in close proximity due to triplex formation. No reaction occurred when the ruthenium complex was not in proximity to the stilbene pair. The wavelength of visible light used was of lower energy than the wavelength of UV light necessary for direct excitation of stilbene. Quantum chemical calculation indicated that ruthenium complex catalyzed the photocycloaddition via triplet‐triplet energy transfer. Site selectivity of this photo‐crosslinking system was evaluated using a DNA duplex bearing two stilbene pairs as a substrate; we showed that the site of crosslinking was precisely regulated by the sequence of the oligonucleotide linked to the ruthenium complex. Since this method does not require orthogonal photoresponsive molecules, it will be useful in construction of complex photoresponsive DNA circuits, nanodevices and biological tools.

Site-Selective Photo-Crosslinking of Stilbene Pairs in a DNA Duplex Mediated by Ruthenium Photocatalyst.

We herein report a method for site-selective photo-crosslinking of a DNA duplex. A stilbene pair was introduced into a DNA duplex and a ruthenium complex was conjugated with a triplex-forming oligonucleotide. We demonstrated that [2+2] photocycloaddition of the stilbene pair occurred upon irradiation with visible light when the ruthenium complex was in close proximity due to triplex formation. No reaction occurred when the ruthenium complex was not in proximity to the stilbene pair. The wavelength of visible light used was of lower energy than the wavelength of UV light necessary for direct excitation of stilbene. Quantum chemical calculation indicated that ruthenium complex catalyzed the photocycloaddition via triplet-triplet energy transfer. Site selectivity of this photo-crosslinking system was evaluated using a DNA duplex bearing two stilbene pairs as a substrate; we showed that the site of crosslinking was precisely regulated by the sequence of the oligonucleotide linked to the ruthenium complex. Since this method does not require orthogonal photoresponsive molecules, it will be useful in construction of complex photoresponsive DNA circuits, nanodevices and biological tools.

The RNA-Binding Domain of hnRNP U Extends beyond the RGG/RG Motifs.

Heterogeneous nuclear ribonucleoprotein U (hnRNP U) is a ubiquitously expressed protein that regulates chromatin architecture through its interactions with numerous DNA, protein, and RNA partners. The RNA-binding domain (RBD) of hnRNP U was previously mapped to an RGG/RG motif within its disordered C-terminal region, but little is understood about its binding mode and potential for selective RNA recognition. Analysis of publicly available hnRNP U enhanced UV cross-linking and immunoprecipitation (eCLIP) data identified high-confidence binding sites within human RNAs. We synthesized a set of diverse RNAs encompassing 11 of these identified cross-link sites for biochemical characterization using a combination of fluorescence anisotropy and electrophoretic mobility shift assays. These in vitro binding experiments with a rationally designed set of RNAs and hnRNP U domains revealed that the RGG/RG motif is a small part of a more expansive RBD that encompasses most of the disordered C-terminal region. This RBD contains a second, previously experimentally uncharacterized RGG/RG motif with RNA-binding properties comparable to those of the canonical RGG/RG motif. These RGG/RG motifs serve redundant functions, with neither serving as the primary RBD. While in isolation, each RGG/RG motif has modest affinity for RNA, together they significantly enhance the association of hnRNP U with RNA, enabling the binding of most of the designed RNA set with low to midnanomolar binding affinities. Identification and characterization of the complete hnRNP U RBD highlight the perils of a reductionist approach to defining biochemical activities in this system and pave the way for a detailed investigation of its RNA-binding specificity.

Structure and dynamics heterogeneity in poly(vinyl acetal)s: The effect of side group length

Understanding on the structure and dynamics of poly(vinyl acetal)s is insufficient due to the complicated chemical structure and amorphous nature of this type of polymers. In this work, we investigate the effect of side group length on structure and dynamics heterogeneity at different length scales spanning from side group, segment, and polymer network by combing dynamic mechanical analysis (DMA), dielectric relaxation spectroscopy (DRS), solid-state NMR, and differential scanning calorimetry analysis (DSC). By increasing the length of acetal side group, its intrinsic dynamics slows down. Taking into account the scale of segment and networks, with the increase of acetal group length, the formation of cross-linking sites formed by the hydroxyl-rich domain is suppressed, the relaxation distribution of the segment widens, and the volume fraction of rigid component decreases. The effect of side group length on the structure and dynamics heterogeneity of poly(vinyl acetal)s at different scales results in significant changes in material properties such as the non-monotonic change in loss factor value (tan δ) and a monotonous reduction in glass transition temperature (Tg).

Preparation of high performance membrane via one-step polymerization and co-deposition of polydopamine/zwitterionic monomers/poly(ethylene glycol) diacrylate

Membrane separation is an effective method for water purification. However, conventional preparation processes for the membranes usually suffer from complicated production technology and lack versatility. Mussel-inspired chemistry has generated extensive interest in exploring a facile strategy for the preparation of polymeric membranes. In this work, a simple, green and time saving strategy is proposed for accomplishing the surface functionalization via one-step polymerization and co-deposition of dopamine/zwitterion/poly(ethylene glycol) diacrylate (PEGDA). The chain segment of the zwitterion can tightly bind water molecules upon the membrane surface, enhancing the hydrophilicity of the membrane. The chain segment of PEGDA can offer cross-linking sites during the co-deposition process, facilitating the formation of the network structure. The retention to dyes for the membranes prepared with PEGDA was higher than those membranes prepared without PEGDA. The optimized membrane exhibited high water permeance up to 25.9 L m−2 h−1 bar−1, with rejection of 99.7 % and 99.6 % for Methyl blue and Congo Red. Meanwhile, the anti-bacterial rate for the optimized membrane reaches 75.9 %, and the water flux recovery rate (FRR) is as high as 86.65 %. The results cast a light on the exploration of the PDA-based NF membranes, featuring simple production technology and versatile capabilities for the separation of various dyes.

Enhancing protein dynamics analysis with hydrophilic polyethylene glycol cross-linkers.

Cross-linkers play a critical role in capturing protein dynamics in chemical cross-linking mass spectrometry techniques. Various types of cross-linkers with different backbone features are widely used in the study of proteins. However, it is still not clear how the cross-linkers' backbone affect their own structure and their interactions with proteins. In this study, we systematically characterized and compared methylene backbone and polyethylene glycol (PEG) backbone cross-linkers in terms of capturing protein structure and dynamics. The results indicate the cross-linker with PEG backbone have a better ability to capture the inter-domain dynamics of calmodulin, adenylate kinase, maltodextrin binding protein and dual-specificity protein phosphatase. We further conducted quantum chemical calculations and all-atom molecular dynamics simulations to analyze thermodynamic and kinetic properties of PEG backbone and methylene backbone cross-linkers. Solution nuclear magnetic resonance was employed to validate the interaction interface between proteins and cross-linkers. Our findings suggest that the polarity distribution of PEG backbone enhances the accessibility of the cross-linker to the protein surface, facilitating the capture of sites located in dynamic regions. By comprehensively benchmarking with disuccinimidyl suberate (DSS)/bis-sulfosuccinimidyl-suberate(BS3), bis-succinimidyl-(PEG)2 revealed superior advantages in protein dynamic conformation analysis in vitro and in vivo, enabling the capture of a greater number of cross-linking sites and better modeling of protein dynamics. Furthermore, our study provides valuable guidance for the development and application of PEG backbone cross-linkers.

Ti3C2Tx MXene- and Sulfuric Acid-Treated Double-Network Hydrogel with Ultralow Conductive Filler Content for Stretchable Electromagnetic Interference Shielding.

Hydrogels are emerging as stretchable electromagnetic interference (EMI) shielding materials because of their tissue-like mechanical properties and water-rich porous cellular structures. However, achieving high-performance hydrogel shields remains a challenge because enhancing conductivity often results in a compromise in deformation adoptability. This work proposes a treatment strategy involving sulfuric acid/titanium carbide MXene, which can simultaneously enhance the conductivity and stretchability of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/poly(vinyl alcohol) (PVA) double-network hydrogels. Multiple spectroscopic characterizations reveal that sulfuric acid promotes the linear conformation transition of the PEDOT molecular chain, while MXene increases charge delocalization and hydrogen bond cross-linking sites. The hydrogels, synthesized with a combined content of 0.6 wt % of MXene and PEDOT:PSS, exhibit an average X-band EMI SE of 41 dB. This performance is sustained at 94.5%, even following stretching and release at a strain of 200%. Interestingly, the EMI SE is found to linearly increase, reaching a value of 99 dB as the frequency is increased to 26.5 GHz. This increase is attributed to the enhanced water molecular polarization process, as supported by theoretical calculations of the impedance and attenuation constant. This work introduces a post-treatment technique that optimizes double-network hydrogels, providing deep insights into their EMI shielding mechanism and enabling high-performance EMI shielding with an ultralow conductive filler content.

A facile method to prepare biobased flexible polydimethylsiloxane − Benzoxazine resin: Dielectric properties and high heat resistance

For the benefit of meet the industrial demand of integrated circuits for low dielectric constant (k) and the environmental requirements of sustainable development, it is important to prepare biobased benzoxazine resin with low k and high heat resistance by solvent-free method. In this paper, the biobased monomer V-fa containing aldehyde group was synthesized by biobased raw materials furfurylamine and vanillin, and then reacted with amino-terminated polydimethylsiloxane (PDMS) to prepare benzoxazine monomer V-fa-pdms containing schiff base structure by a solvent-free method. Then, the monomer was cured to obtain biobased benzoxazine resin poly(V-fa-pdms), and the heat resistance, mechanical and dielectric properties of poly(V-fa-pdms) were studied. The results indicate that the resin exhibits excellent thermal stability and toughness by combining benzoxazine and PDMS reasonably. The initial thermal decomposition temperature (Tdi, 5% thermogravimetric loss) is 387 °C, and the material also exhibits excellent dielectric properties. When the frequency increases from 1 Hz to 1 MHz, the k of the material decreases from 2.71 to 2.60, and the fluctuation range of dielectric loss is 0.0051–0.0049. With the increase of frequency, both k and dielectric loss show a downward trend. At the same time, the material shows good corrosion resistance in commonly used solvents. These excellent properties of poly(V-fa-pdms) are due to the existence of a high cross-linked network structure formed by multiple cross-linking sites in the polymer network and the combined effect of low k and high heat-resistant PDMS components.

Reinforced, self-healing, recyclable rubber materials based on multiple dynamic bond constructs crosslinked with chemical groups

Enhancing the mechanical attributes of traditional rubber, while simultaneously imparting superior self-healing and recyclability, remains a formidable task within the realm of polymer science. In this study, we introduce, for the inaugural time, the utilization of metal–ligand interactions to amalgamate chemical cross-linking sites within a styrene-butadiene rubber matrix. This approach facilitates the creation of a fortified, self-healing, and recyclable rubber composite, interconnected by an array of dynamic bonds within a singular chemical entity. This chemical assembly engenders a microphase-separated architecture that exhibits reinforcement and resistance to creep. In addition, the presence of reversible oxime-carbamate and metal–ligand bonds bestow the rubber composites with remarkable self-healing and recyclability. Notably, the self-healing efficiency reached an impressive 87%, while the recyclability retention hovered between 85 and 91% (in terms of tensile strength) post multiple reprocesses. This research paves a novel avenue for the fabrication of rubber composites that are robust, self-healing, and recyclable.

Osnovni principi otkrivanja oštećenja DNK pomoću alkalnog komet testa

The Comet assay is a highly sensitive and rapid method for detecting DNA damage at the level of individual cells. It measures single-stranded and double-stranded DNA breaks, alkali-labile, incomplete excision repair and cross-linking sites. A major advantage of the Comet assay is its applicability to both proliferating and non-proliferating cells, and it can be performed on all types of eukaryotic cells. The basic principle of the alkaline Comet assay is to lyse the biological membranes to release proteins bound to the DNA, followed by a short-term electrophoresis at a pH above 13. Through this process, the DNA fragments migrate and form a comet-like shape, which is visualized by staining with a DNA-binding fluorescent dye. The extent of electrophoretic migration is proportional to the amount of DNA damage. Key advantages of the Comet assay include sensitivity-the assay can detect low levels of DNA damage, versatility-it can be used with a small amount of test substance, speed-results are usually available within 24 to 48 hours, and broad applicability-the method is suitable for numerous purposes, including molecular epidemiology, occupational exposure studies, environmental biomonitoring, antigenotoxicity assessments and clinical research. Overall, the Comet assay provides valuable data for a range of scientific and clinical fields, making it a versatile and powerful tool for assessing DNA damage.

Engineering a polyvinyl butyral hydrogel as a thermochromic interlayer for energy-saving windows.

Achieving mastery over light using thermochromic materials is crucial for energy-saving glazing. However, challenges such as high production costs, limited durability, and recyclability issues have hindered their widespread application in buildings. Herein, we develop a glass interlayer made of a polyvinyl butyral-based hydrogel swollen with LiCl solution. In addition to a fast, isochoric, and reversible transparency-to-opacity transition occurring as ambient temperatures exceed thermally comfortable levels, this hydrogel uniquely encompasses multiple features such as frost resistance, recyclability, scalability, and toughness. The combination of these features is achieved through a delicate balance of polyvinyl butyral's amphiphilicity and the suppression of network-forming phase separation. This design endows a nanostructured polyvinyl butyral-LiCl composite gel with swollen molecular segments linked by dispersed cross-linking sites in the form of hydrophobic nano-nodules. Upon laminating this hydrogel (a thickness of 0.3 mm), the resultant glazing product demonstrates approximately 90% luminous transmittance even at sub-zero temperatures, along with a significant modulation of solar and infrared radiation at 80.8% and 68.5%, respectively. Through simulations, we determined that windows equipped with the hydrogel could reduce energy consumption by 36% compared to conventional glass windows in warm seasons. The widespread adoption of polyvinyl butyral in construction underscores the promise of this hydrogel as a thermochromic interlayer for glazing.