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The industrial food applications of native starches are limited due to their limited resistance to shear, susceptibility to thermal decomposition, and high tendency for retrogradation. Cross-linking of starches adds intra and inter-molecular bonds at various locations in the starch molecule that result in the stability of the granule and enhance functional attributes. This process involves the use of various cross-linking agents such as sodium trimetaphosphate (STMP), sodium tripolyphosphate (STPP), epichlorohydrin (EPI), phosphorus chloride (POCl3), and citric acid, etc., to introduce covalent or non-covalent linkages between starch molecules. Cross-linked starch exhibits improved resistance to retrogradation, enhanced freeze-thaw stability, and increased stability during cooking, shearing, and processing, such as high or low temperatures and pH. This review paper offers an overview of cross-linking modifications, emphasizing their importance in addressing native starch limitations. It underscores the significance of selecting appropriate cross-linking agents to customize starch properties for specific applications. Furthermore, the paper discusses the properties and applications of cross-linked starches and delves into regulatory considerations regarding their use. Regulatory consideration for cross-linked starches has also been discussed. Cross-linking modifications offer a promising avenue to unlock the full potential of starch and expand its utility across a wide range of applications. [ABSTRACT FROM AUTHOR]

Composite material based on polyethylene glycol (PEG) and polypyrrole (PPy) polyrotaxanes both encapsulated into α‐cyclodextrins (α‐CDs) macrocycle molecules was synthesized by cross‐linking reaction. The effect of PPy‐αCD polyrotaxane incorporation into the PEG‐αCD polyrotaxane matrix, on the structural, morphological, thermal, and dielectric properties was evaluated and compared to the reference material. Scanning electron microscopy spectroscopy indicates different surface morphologies of this material in comparison to the reference one. In addition, the contact angle measurements and surface free energy attest a hydrophilic surface, while the reference material exhibits a hydrophobic surface. More than that, the presence of the PPy‐αCD cross‐linked into the matrix has a beneficial effect on the thermal properties. The composite material shows an enhanced dielectric constant value of 31,365 at 10 Hz frequency compared to the 38.2 of the reference material, and higher dielectric loss (62,398 vs. 80 at 10 Hz, respectively). The conductivity measurements at 10 Hz frequency indicated for the reference material the value 4.5 × 10−11, while for the material with PPy‐αCD polyrotaxane, the conductivity is three orders of magnitude higher (3.5 × 10−8) confirming the improvements of the electrical properties. [ABSTRACT FROM AUTHOR]

Purpose: To assess the short and mid-term outcomes of epithelium-off (epi-off) corneal collagen cross-linking using Riboflavin with Vitamin E TPGS (Epi-off Ribocross® CXL) for progressive keratoconus (KC). Design: Retrospective, single-center non-comparative interventional study. Methods: Patients with progressive keratoconus who underwent CXL using (Epi-off Ribocross® CXL) from May 2021 to May 2022 who completed at least 12 months of follow-up in Humanitas Clinical and Research Center, Rozzano, Milan, Italy. Corrected distance visual acuity with spectable (CDVA), tomographic parameters (Belin ABCD) and topographic parameters were evaluated at baseline and at last follow up. Results: Twenty eyes of twenty patients fulfilled inclusion criteria. CDVA remained stable at last follow up (0.88 ± 0.19 from 0.83 ± 0.21, p = 0.45) with a significant reduction in cylinder (1.97 ± 1.69 from 2.78 ± 2.19, p = 0.03). Kmax significantly improved from 53.18D ± 6.32 to 50.96 ± 5.3D (p = 0.005). At the last follow up, no case of progression was noted. Conclusions: Epi-off Ribocross® CXL proved to be a safe treatment for progressive KC, with a stabilization of all cases at the one year follow up. Further studies are needed to confirm long-term stability. [ABSTRACT FROM AUTHOR]

The durability of anion exchange membranes (AEMs) and the balance between ionic conductivity and dimensional stability have been the focus of research. To this end, we propose a new type of AEMs with vinyl imidazole as the in situ cross‐linking monomer. The rigid‐flexible balance within the membrane was adjusted by changing the arrangement of the internal segments of the polymer and introducing different monomers into the main chain. The results showed that the performance of AEMs could be effectively improved by adopting an ether‐free backbone and a cationic cross‐linking strategy. The swelling rate of all AEMs was less than 20%. The ionic conductivity of BDCP‐80 reached 102.74 mS cm−1 at 80°C. Alkaline stability tests showed that the ionic conductivity of all AEMs remained above 82% after 720 h immersion in 2 M NaOH solution at 80°C. This study demonstrated that the simple in situ cross‐linking method can effectively improve the overall performance of AEMs and provide an effective way to develop high‐performance AEMs. [ABSTRACT FROM AUTHOR]

Iodothyronine deiodinases (Dio) are selenocysteine-containing membrane enzymes that activate and inactivate the thyroid hormones (TH) through reductive iodide eliminations. The three deiodinase isoforms are homodimers sharing highly conserved amino acid sequences, but they differ in their regioselectivities for the deiodination reaction and regulatory features. We have now solved a crystal structure of the mouse deiodinase 2 (Dio2) catalytic domain. It reveals a high overall similarity to the deiodinase 3 structure, supporting the proposed common mechanism, but also Dio2-specific features, likely mediating its unique properties. Activity studies with an artificially enforced Dio dimer further confirm that dimerization is required for activity and requires both the catalytic core and the enzyme's N-terminus. Cross-linking studies reveal the catalytic core's dimerization interface, providing insights into the architecture of the complete, active Dio homodimer. [ABSTRACT FROM AUTHOR]

The lack of fat in yogurt can lead to alterations in taste and whey separation, reducing consumer acceptance. In this study, the feasibility of enhancing the quality of skim milk yogurt through a combination of transglutaminase (TG) and protein-glutaminase (PG) was investigated. The combination of TG and PG resulted in simultaneous cross-linking and deamidation of CN micelles, with PG deamidation taking priority over TG cross-linking, leading to higher solubility and lower turbidity of milk proteins compared with TG alone. When 0.06 U/mL TG and 0.03 U/mL PG were added, firmness and viscosity indexes significantly increased by 38.26% and 78.59%, respectively, as compared with the control. Microscopic images revealed increased cross-linking with CN and filling of cavities by smaller submicelles in the combination of TG and PG treatment. Furthermore, the combination of TG and PG resolved issues of rough taste and whey separation, leading to improved overall liking. This study highlights the benefits of using both enzymes in dairy production and has important implications for future research. The list of standard abbreviations for JDS is available at adsa.org/jds-abbreviations-24. Nonstandard abbreviations are available in the Notes. [Display omitted] [ABSTRACT FROM AUTHOR]

Over the years, studies showed that hydrogels can be produced through synthetic route to overcome the limitations in obtaining natural-based hydrogels. Biomass resources offer potential alternatives as renewable feedstocks due to their outstanding biodegradability and biocompatibility. Oil palm mesocarp fiber (MF) is the biomass residue obtained after the pressing of palm fruits during palm oil extraction. There is approximately 11 % MF generated from palm fruits after oil extraction. However, the applications of MF are limited. This study aimed to investigate the development of hydrogels from holocellulose MF instead of commonly used cellulose which involving several pretreatment steps, through acid cross-linkers. Holocellulose MF was selected as polymer for chemical cross-linking with two inexpensive and nontoxic hydrophilic organic acids, citric acid and acetic acid for hydrogel production. Comparison study was carried out to evaluate the physicochemical properties, and degree of swelling, as well as gel content in different media for both acids in the production of hydrogel from holocellulose MF. Results indicated that the optimum concentrations of citric acid and acetic acid for gel content and degree of swelling were 5 M and 2 M, respectively. Both optimized hydrogels exhibited comparable profiles in terms of morphology, thermal stability and functional groups, in addition to showing similar degree of swelling profile in different media, i.e., salt solution, acidic, neutral to alkaline, implying their distinctive characteristics. In summary, holocellulose MF is suitable for the production of hydrogel with citric acid and acetic acid as crosslinkers for different desired applications. [ABSTRACT FROM AUTHOR]

Hyaluronic acid (HA) is a commonly used injectable material in temporary vocal fold injections (VFI) in patients with unilateral vocal fold paralysis (UVFP). Hyaluronic acid has generally been known for its three–six months of longevity following VFI. Owing to recent advances in cross-linking technologies, the longevity of HA-based materials, including deep-volumizing cross-linked HA used in VFI, has been improved. However, persisting injectable material in the subepithelial space poses undesirable complications following VFI. Herein, we report 2 cases of unexpected persistence of superficially injected cross-linked HA. In the first case, a 70-year-old man with iatrogenic UVFP received VFI with cross-linked HA three years ago and was referred for persistent dysphonia. Previously injected HA spilled out from the vocal fold (VF) when an epithelial incision was made in the subepithelial cystic lesion. In the second case, a 72-year-old woman with iatrogenic UVFP received VFI with cross-linked HA that migrated into the subepithelial space. Diffuse swelling of the injected VF caused dysphonia that lasted for a year. The previously injected HA spilled out when an epithelial incision was made in the swollen VF. Since superficially injected deep-volumizing cross-linked HA can persist for up to three years, laryngologists should be aware of possible sequelae upon suboptimal VFI with cross-linked HA. [ABSTRACT FROM AUTHOR]

This study investigated the prospective effect of ApnA enzyme under different concentrations (µL/100 mL soymilk) compared to chemical (pH, MgCl2, and K-carrageenan, respectively) as tofu coagulants. The resultant tofu samples were analyzed for compositional analysis, thermal properties, water distribution, and microstructure properties. The higher concentration of enzyme used, the higher resulted moisture content of tofu. ApnA enzyme increased the cross-linking through protein molecules and trapped more water within the gel network. Tofu samples prepared by different concentrations of ApnA enzyme displayed significantly less freezable water content (15.44, 12.84, and 19.46 g/100 g). In particular, 800 µL ApnA/100 mL soymilk formed an interconnected gel matrix with regular distribution with almost invisible cavities. The thermal pretreatment and the increased coagulation time might encourage this irregular structure. On the other hand, the gel network coagulated using the reduction of pH showed a weaker gel due to an accelerated acidification. [ABSTRACT FROM AUTHOR]

Long afterglow nanoparticles, a type of luminescence material, may gradually release stored light energy even after the excitation light has stopped. The modification of polymer membranes by introducing long afterglow nanoparticles via an inorganic particle mixtures, broaden their uses in biomedicine field. In this study, a new membrane modification approach was employed to reduce the loss of physical–mechanical performance, caused by inherent strontium aluminate inorganic particle aggregation. Moreover, eugenol, a cross-linking agent, was used to interact with acrylate monomers to form locally cross-linked compounds using an ex situ approach that improves strontium aluminate particle dispersion. Furthermore, the soap-free emulsion polymerization method used, regulates the degree of cross-linking in the membrane, hence addressing nanoparticles agglomeration. Results showed that the cross-linked structure of the membrane produced improves the heat stability and the hydrophobicity of the material produced while also increasing the nanoparticles dispersion as evidenced by the XRD study. Nevertheless, membranes with cross-linking agents outperformed in water droplet trials by not breaking or whitening the droplets. Furthermore, the generated membranes exhibit high antibacterial activity, making them attractive for paramedical applications such as protective membranes applied on the top of the skin or on the surface areas of sensors, microneedles and metal fasteners. [ABSTRACT FROM AUTHOR]

Lead halide perovskite solar cells (PSCs) have demonstrated power conversion efficiencies comparable to silicon‐based solar cells, yet their instability under environmental stressors, such as humidity, heat, and light, remains a significant barrier to commercialization. A primary cause of this instability is the uncoordinated lead ions (Pb2+), which accelerates the degradation of PSCs and pose environmental concerns due to potential lead leakage. Recently, the introduction of ligands into PSCs has shown promise in mitigating lead toxicity through effective passivation, primarily by forming hydrogen bonds (H‐bonds) between functional groups of the ligands and the perovskite structure. In this minireview, we explore the critical role of H‐bonds in stabilizing PSCs by enhancing the structural integrity of the perovskite layer and reducing lead leakage. Furthermore, we discuss the contribution of these ligands in defect passivation, hydrophobicity, self‐encapsulation, cross‐linking, and self‐healing mechanisms. These insights will highlight the multi‐functional capabilities of ligands in improving the long‐term stability and durability of PSCs, offering pathways to address current challenges in their commercialization. [ABSTRACT FROM AUTHOR]

Background: To determine if cross‐linking (CXL) treatment modifies any pre‐existing association between corneal optical density (COD) and age in keratoconus free of corneal scarring. Methods: COD was monitored in two groups (i) before and after standard CXL treatment for keratoconus (de‐epithelization with a crescent blade, n = 69 eyes) and (ii) age/gender‐matched cases without any signs of keratoconus (n = 24 eyes). Seven different markers of COD were quantified using a 0–100 grey scale, supplied with Pentacam™ software. Results: Mean age (±sd, range) in Group I (19 females and 50 males) was 24.2 years (±7.2, 11–44) and in Group II (9 females and 15 males), it was 24.7 years (±7.6, 17–45). COD over the apex and along the depth of the cornea (y, arbitrary scale units) was associated with age (x, in years) in Group I at preop (y = 0.08x + 13.12, rs = 0.350 and p = 0.003), at 12 months postop (y = 0.08x + 15.15, rs = 0.295 and p = 0.014) and in Group II, at the start (y = 0.16x + 11.28, rs = 0.474 and p = 0.019) and 12 months later (y = 0.24x + 8.63, rs = 0.600 and p = 0.002). The change in COD following CXL was significantly associated with the preop value. Conclusion: CXL initially breaks down the pre‐existing relationship between COD and age. This is re‐established by 12 months postop. The CXL induced change in COD depends on the preop value but not on the patient's age. [ABSTRACT FROM AUTHOR]

One of the few synthetic resins from petroleum-based sources that are biodegradable and can reduce the environmental pollution is polyvinyl alcohol (PVA). PVA film is non-toxic, transparent, and biocompatible in line with green ecologically friendly requirements. It is completely biodegradable and possesses good mechanical properties, chemical resistance, and gas barrier. PVA's hydroxyl groups, however, decrease its mechanical and thermal properties and make it water-soluble, which limits its use. However, it is possible to control the water solubility or absorption by partially cross-linking the polymer chains. This work aims to enhance the mechanical properties while making an insoluble film through cross-linking with oxalic acid (OA). In the present investigation, PVA film was cross-linked with OA (with variable weight percentage (wt%) of OA) to limit its ability to absorb moisture. Tensile testing was utilized to evaluate the mechanical properties of the films, revealing their ultimate tensile strength, % elongation, and Young's modulus. With increase in wt% of OA, % elongation of PVA-based films decreases, whereas maximum tensile strength was observed at 10 wt% of OA configuration. In comparison to neat PVA, the differential thermo-gravimetric analysis peak migrated towards the higher temperature side with an increase in the OA concentration. The peak value of tan δ curve also increased and shifted towards higher temperature side as the OA concentration increased. This concludes that prepared films have high damping coefficient and can absorb impact load. Finally, the films' creep-recovery behaviour was also examined in detail. To represent the potential application of these films as packaging materials, anti-microbial tests were also conducted. [ABSTRACT FROM AUTHOR]

Ultraviolet (UV), visible, and near‐infrared (NIR) broadband organic photodetectors are fabricated by sequential solution‐based thin film coatings of a polymer electron blocking layer (EBL) and a polymer photoactive layer. To avoid damage to a preceding polymer EBL during a subsequent solution‐based film coating of a polymer photoactive layer due to lack of solvent orthogonality, 2‐(((4‐azido‐2,3,5,6‐tetrafluorobenzoyl)oxy)methyl)−2‐ethylpropane‐1,3‐diyl bis(4‐azido‐2,3,5,6‐tetrafluorobenzoate) (FPA‐3F) is used as a novel organic cross‐linking agent activated by UV irradiation with a wavelength of 254 nm. Solution‐processed poly[N,N′‐bis(4‐butylphenyl)‐N,N′‐bis(phenyl)‐benzidine] (poly‐TPD) films, which are cross‐linked with a FPA‐3F photocrosslinker, are used for a preceding polymer EBL. A ternary blend film composed of PTB7‐Th, COi8DFIC, and PC71BM is used as a NIR‐sensitive organic photoactive layer with strong photosensitivity in multispectral (UV–visible–NIR) wavelengths of 300–1,050 nm. Poly‐TPD films are successfully cross‐linked even with a very small amount of 1 wt% FPA‐3F. Small amounts of FPA‐3F have little detrimental effect on the electrical and optoelectronic properties of the cross‐linked poly‐TPD EBL. Finally, organic NIR photodetectors with a poly‐TPD EBL cross‐linked by the small addition of FPA‐3F (1 wt%) show the detectivity values higher than 1 × 1012 Jones for the entire UV–visible–NIR wavelengths from 300 nm to 1050 nm, and the maximum detectivity values of 1.41 × 1013 Jones and 8.90 × 1012 Jones at the NIR wavelengths of 900 and 1000 nm, respectively. [ABSTRACT FROM AUTHOR]

Collagen has shown promising potential in biomedical fields due to its high biocompatibility, abundance of resources, ease of flexible modification, and potential for active targeting. The biomedical capacity is largely influenced by their unique structure and properties. Collagen is typically extracted from tissues and organs that are commonly discarded as waste. The extraction of collagen from agricultural and sideline resources is an environmentally friendly method for utilizing byproducts and generating high-value products. The extraction methods can significantly impact the structure and composition. Collagens can be cross-linked using external reagents or techniques to enhance their strength and meet growing demands. This review will discuss the recent advancements in collagen-based biomaterials for chronic wound healing, bone regeneration, and cornea defect repair, focusing on extraction and modification strategies. We are dedicated to bridging the gap between the pretreatment of collagens in various processes and their specific applications. This will facilitate the scientific design and optimal utilization of collagen-based biomaterials for tissue regeneration. This review provides readers with a comprehensive understanding of the advancements in extraction methods, cross-linking strategies, and the biomedical applications of collagen. [ABSTRACT FROM AUTHOR]

Hyaluronic acid (HA) fillers are extensively utilized in aesthetic medicine due to their biocompatibility, reversibility, and effectiveness in enhancing skin hydration, volume, and overall appearance. These fillers are predominantly produced through microbial fermentation, followed by a critical cross-linking process that enhances their longevity by resisting enzymatic degradation. This review provides a thorough examination of the manufacturing processes that differentiate HA fillers, with particular attention to the distinctions between biphasic and monophasic variants. Unlike previous studies, this review emphasizes the specific cross-linking techniques and their substantial impact on the fillers' rheological properties, such as elasticity and cohesiveness, which are crucial to their clinical performance and patient outcomes. Additionally, the review offers a comprehensive comparison of HA fillers with non-HA alternatives, including calcium hydroxylapatite, poly-l-lactic acid, and polymethyl methacrylate, highlighting the unique advantages and potential complications associated with each type. By presenting novel insights into the latest advancements and challenges in filler technology, this review aims to provide clinicians with a deeper understanding of filler properties, thereby guiding them in making informed decisions to optimize patient safety and aesthetic results. [ABSTRACT FROM AUTHOR]

Raising the cutoff voltage can efficiently increase the energy density of lithium cobalt oxide (LCO). However, upon charging over 4.55 V the LCO undergoes irreversible phase transition from the pristine O3 phase to the metastable H1‐3 phases, causing serious side reactions, which results in poor cycling stability. Herein, a multifunctional aqueous composite binder derived from the cross‐linking of fucoidan (FUC) and polyacrylamide (PAM) is developed to enhance the stability of LCO cathode at 4.6 V. The cross‐linking interaction of FUC and PAM provides a uniform coating on the surface of LCO and ensures a high peel strength for the electrode, effectively mitigating irreversible phase transition and detrimental interface side reactions. More importantly, the sulfur ester and amide groups of FUC‐PAM favorably function as surface charge compensators to the high valent Co upon charging under high voltages, thus stabilizes the surface lattice of LCO and suppresses the detrimental oxygen release. As expected, the LCO with a cutoff voltage of 4.6 V exhibits a high capacity retention of 90% after 100 cycles at a current density of 110 mA g−1. The interfacial coordination effect of composite binders offers a novel strategy to enhance the stability of high‐voltage LCO for high‐energy lithium‐ion batteries. [ABSTRACT FROM AUTHOR]

Cross-linkable hole-transporting materials with a new cross-linking group, benzocyclobutene, are designed and synthesized. These materials dissolve well in common organic solvents and exhibit excellent solvent resistance after thermal cross-linking. Electroluminescent (EL) devices were fabricated using these two hole-transporting materials. [ABSTRACT FROM AUTHOR]

The burning and melting of elastic fastening bands in high-temperature environments are major contributors to empyrosis and ambustion owing to their snug fit to human body parts in practical usage. Conventionally fabricated fastening bands show poor degradation, negative environmental impact, and poor flame-retardant performance. Herein, we report an ecofriendly cyclic phosphate ester-based flame-retardant polylactic acid (PLA) elastic band prepared using an impregnation-baking process, and experimental investigation was conducted on the optimized finishing process. The band was characterized using scanning electron microscopy, energy-dispersive spectroscopy, and thermogravimetry. The band exhibited a damage length of 3.9 cm after vertical combustion and self-extinguishing effect after being removed from the fire source without generating molten droplets. The cross-linking phenomenon between the modified PLA fibers was beneficial in improving the flame retardancy of the PLA elastic band in the condensed phase. The strength loss of the band was <5%. Thus, the prepared band can be widely used in real-world applications. [ABSTRACT FROM AUTHOR]

With the increasing development of productivity, new materials that allow for the efficient use of energy are slowly becoming a sought-after goal, as well as a challenge that is currently being faced. For this reason, we have made aerogels as the target of our research and prepared different series (CLPI (1–5)) of cross-linked polyimide aerogels by mixing and cross-linking the heat-insulating cross-linking agent 1,3,5-tris(4-aminobenzylamino)benzene (TAB) with polyamic acid solution. We created a three-dimensional spatial organization by using vacuum freeze-drying and programmed high-temperature drying, then controlled the concentration of the polyamidate solution to investigate the concentration and TAB's influence on aerogel-related properties. Among them, the shrinkage is reduced from 40% in CLPI-1 to 28% in CLPI-5, and it also shows excellent mechanical characteristics, the highest compression strength (CLPI-5) reaches 0.81 MPa and specific modulus reaches 41.95 KN m/Kg. In addition, adding TAB improves the aerogel thermal resistance, T5 in N2 from PI-2 519 °C to CLPI-2 556 °C. The three-dimensional network-type structure of the aerogel shows an excellent thermal insulation effect, where the thermal conductivity can be as low as 24.4 mWm−1 K−1. Compared with some protective materials, cross-linked polyimide aerogel presents better flame-retardant properties, greatly improving the scope of its application in the industrial protection. [ABSTRACT FROM AUTHOR]

Suitably modified sesbania gum as a biodegradable functional biomaterials was very attractive in many applications. Therefore, a combination of cross‐linking, carboxymethylation, and oxidation was chosen to modify sesbania gum (SG) to expand its use. The experimental results indicated that cross‐linking could be completed not only on SG particles, but also between different SG particles. The cross‐linking decreased the number of surface hydroxyl groups on SG. The sedimentation volume decreased with the increase of phosphorus content of cross‐linked sesbania gum (CLSG). The structure of SG particles was severely disrupted by carboxymethylation and oxidation, while the structure was less affected by cross‐linking. The viscosities of SG and modified SG paste in acidic medium were less than those in neutral medium, while their viscosities in alkaline medium were more than those in neutral medium. Cross‐linking, carboxymethylation, and oxidation could ameliorate the retrogradation of SG, but decrease its swelling power, freeze–thaw stability, acid, and alkaline resistance. The aldehyde groups had good antibacterial activity against Trichoderma harzianum, whereas the carboxymethyl groups and phosphate ester groups showed poor antimicrobial activity against T. harzianum. [ABSTRACT FROM AUTHOR]

The industrial food applications of native starches are limited due to their limited resistance to shear, susceptibility to thermal decomposition, and high tendency for retrogradation. Cross-linking of starches adds intra and inter-molecular bonds at various locations in the starch molecule that result in the stability of the granule and enhance functional attributes. This process involves the use of various cross-linking agents such as sodium trimetaphosphate (STMP), sodium tripolyphosphate (STPP), epichlorohydrin (EPI), phosphorus chloride (POCl3), and citric acid, etc., to introduce covalent or non-covalent linkages between starch molecules. Cross-linked starch exhibits improved resistance to retrogradation, enhanced freeze-thaw stability, and increased stability during cooking, shearing, and processing, such as high or low temperatures and pH. This review paper offers an overview of cross-linking modifications, emphasizing their importance in addressing native starch limitations. It underscores the significance of selecting appropriate cross-linking agents to customize starch properties for specific applications. Furthermore, the paper discusses the properties and applications of cross-linked starches and delves into regulatory considerations regarding their use. Regulatory consideration for cross-linked starches has also been discussed. Cross-linking modifications offer a promising avenue to unlock the full potential of starch and expand its utility across a wide range of applications.

In this case series, we will describe sterile keratitis in the early postoperative period after hypotonic collagen cross-linking (CXL) in two pediatric cases. This is a retrospective case series of two eyes of two children who developed inflammatory keratitis with central corneal haze after uneventful epithelial-off hypotonic CXL. After ensuring microbiological sterility, appropriate treatment with topical steroids and lubricants was started. There was complete resolution of corneal infiltrates with minimal scarring. Both patients regained almost the preoperative best-corrected visual acuity of 20/80 and 20/60, respectively.

Abstract Background Pectin from Taiwan Citrus depressa Hayata’s peels (CDH pectin) and sodium alginate (Na alginate) were mixed in neutral acidity to produce microhydrogel beads or microspheres. The potential use of the microspheres such as encapsulation materials for quercetin and nobiletin, DPPH (2,2-diphenyl-1-picrylhydrazyl) scavenging activity, toxic elements absorption ability, and thermal characteristics were explored. Results Different ratios of CDH pectin and Na alginate produced microspheres of varying sizes and shapes. The highest yield (47.59%) with the broadest diameter was obtained at a Na alginate—CDH pectin ratio of 2:1, while the smallest yield was obtained from Na alginate—CDH pectin ratio of 1:3 (24.13%). Increasing the amount of Na alginate resulted in more spherical microspheres, higher heavy metals (cobalt and nickel) removal rates, yet a lower swelling ratio. A high pectin concentration also increased the encapsulation efficiency of quercetin and nobiletin, reaching 91.5% and 86.74%, respectively. Quercetin and nobiletin release analysis (in vitro) showed a slow release of drugs from the microspheres. Less than 20% quercetin and nobiletin were released from the microspheres in SGF (simulated gastric fluid) pH 1.2 solution after 2 h and more than 40% of the encapsulated drug was released in SIF (simulated intestinal fluid) pH 6.8 after 4 h. The strong DPPH scavenging activity of quercetin (99%) was not hindered by encapsulation materials. ICP-OES (inductively coupled plasma–optical emission spectrometry) analysis demonstrated that the biopolymer can absorb cobalt and nickel from water. Thermogravimetric analysis (TGA) result showed that the combination of CDH pectin and Na alginate produced a biopolymer that exhibited a weight loss of only 1.86–4.33% at 100 °C. Conclusions These findings suggest that microspheres produced from CDH pectin cross-linked with sodium alginate had potential in nobiletin and quercetin encapsulation. Moreover, the polymer could absorb heavy metals and exhibit an important characteristic for hot food and beverage packaging applications.

Abstract Effective enzyme stabilization through immobilization is essential for the functional usage of enzymatic reactions. We propose a new method for synthesizing elastic hydroxyapatite microgel (E-HAp-M) materials and immobilizing lipase using this mesoporous mineral via the ship-in-a-bottle-neck strategy. The physicochemical parameters of E-HAp-M were thoroughly studied, revealing that E-HAp-M provides efficient space for enzyme immobilization. As a model enzyme, lipase (LP) was entrapped and then cross-linked enzyme structure, preventing leaching from mesopores, resulting in highly active and stable LP/E-HAp-M composites. By comparing LP activity under different temperature and pH conditions, it was observed that the cross-linked LP exhibited improved thermal stability and pH resistance compared to the free enzyme. In addition, they demonstrated a 156% increase in catalytic activity compared with free LP in hydrolysis reactions at room temperature. The immobilized LP maintained 45% of its initial activity after 10 cycles of recycling and remained stable for over 160 days. This report presents the first demonstration of a stabilized cross-linked LP in E-HAp-M, suggesting its potential application in enzyme-catalyzed processes within biocatalysis technology.

Tunable hydrogels have gained significant attention in the bioengineering field due to their designer preparation approach. Towards this end, gelatine stands out as a promising candidate owing to its desirable attributes, such as biocompatibility, ability to support cell adhesion and proliferation, biodegradability, and cost-effectiveness. This study presents the preparation of a robust gelatine hydrogel employing sacran aldehyde (SDA) as a natural cross-linker. The resulting SDA-cross-linked gelatine hydrogels (GSDA) display an optimal compressive stress of 0.15 MPa at 50% strain, five times higher than pure gelatine hydrogel. As SDA cross-linking concentration is increased, the swelling capacity of GSDA declines. This decline in swelling capacity, from 80% to 40%, is a result of strong crosslinking of gelatin with SDA. Probing further with FT-IR spectroscopy and SEM at the micron scale unveiled a dual-cross-linking mechanism within the hydrogels. This mechanism encompasses both short- and long-range covalent cross-linking, along with thermo-induced physical cross-linking, resulting in a significant enhancement of the load-bearing capacity of the fabricated hydrogels.

Abstract In this work, microcapsules were developed by the complex coacervation of sodium caseinate and pectin as a carrier for saffron extract. Parameters such as Zeta potential, dynamic light scattering, and microscopic techniques were investigated for their influence on the formation of these complexes. Furthermore, Fourier transform infrared (FTIR) analysis confirmed the reaction mechanism between the protein and tannic acid or saffron extract. The study revealed that core/shell and protein/polysaccharide (Pr/Ps) ratios play a role in the encapsulation efficiency (EE) and loading capacity (LC) of saffron extract, with EE and LC ranging from 48.36 to 89.38% and 1.14 to 5.55%, respectively. Thermal gravimetric analysis revealed that the degradation temperature of saffron increased significantly with microencapsulation. The use of tannic acid for hardening the microcapsules led to an increase in size from 13 μm to 27 μm. Rheological findings indicated that shear-thinning behavior in the coacervates, with cross-linking, has a minor effect on the interconnected elastic gel structures. However, cross-linking improved the microcapsules' thermal and structural properties. The increase in polymer chain length due to cross-linking and the presence of the guest molecule (saffron extract) resulted in higher rheological moduli, reflecting enhanced entanglements and correlating well with the thermal, structural, and microstructural properties of the coacervates. Kinetic release studies showed a slower release in the gastric phase compared to the intestinal phase, with the Ritger–Peppas model effectively describing saffron extract release, highlighting a dominant swelling and dissolution release mechanism. Therefore, the NaCas/HMP coacervate wall materials made saffron stable in the gastric stage and sustainably release. It in the intestinal stage, promoting excellent absorption of saffron in simulated digestion. Graphical Abstract

Background: Pectin from Taiwan Citrus depressa Hayata's peels (CDH pectin) and sodium alginate (Na alginate) were mixed in neutral acidity to produce microhydrogel beads or microspheres. The potential use of the microspheres such as encapsulation materials for quercetin and nobiletin, DPPH (2,2-diphenyl-1-picrylhydrazyl) scavenging activity, toxic elements absorption ability, and thermal characteristics were explored. Results: Different ratios of CDH pectin and Na alginate produced microspheres of varying sizes and shapes. The highest yield (47.59%) with the broadest diameter was obtained at a Na alginate—CDH pectin ratio of 2:1, while the smallest yield was obtained from Na alginate—CDH pectin ratio of 1:3 (24.13%). Increasing the amount of Na alginate resulted in more spherical microspheres, higher heavy metals (cobalt and nickel) removal rates, yet a lower swelling ratio. A high pectin concentration also increased the encapsulation efficiency of quercetin and nobiletin, reaching 91.5% and 86.74%, respectively. Quercetin and nobiletin release analysis (in vitro) showed a slow release of drugs from the microspheres. Less than 20% quercetin and nobiletin were released from the microspheres in SGF (simulated gastric fluid) pH 1.2 solution after 2 h and more than 40% of the encapsulated drug was released in SIF (simulated intestinal fluid) pH 6.8 after 4 h. The strong DPPH scavenging activity of quercetin (99%) was not hindered by encapsulation materials. ICP-OES (inductively coupled plasma–optical emission spectrometry) analysis demonstrated that the biopolymer can absorb cobalt and nickel from water. Thermogravimetric analysis (TGA) result showed that the combination of CDH pectin and Na alginate produced a biopolymer that exhibited a weight loss of only 1.86–4.33% at 100 °C. Conclusions: These findings suggest that microspheres produced from CDH pectin cross-linked with sodium alginate had potential in nobiletin and quercetin encapsulation. Moreover, the polymer could absorb heavy metals and exhibit an important characteristic for hot food and beverage packaging applications. [ABSTRACT FROM AUTHOR]

In biomaterials research, using one or two components to prepare materials is common. However, there is a growing interest in developing materials composed of three components, as these can offer enhanced physicochemical properties compared to those consisting of one or two components. The introduction of a third component can significantly improve the mechanical strength, biocompatibility, and functionality of the resulting materials. Cross-linking is often employed to further enhance these properties, with chemical cross-linking agents being the most widely used method. This article provides an overview of the chemical agents utilized in the cross-linking of three-component biomaterials. The literature review focused on cases where the material was composed of three components and a chemical substance was employed as the cross-linking agent. The most commonly used cross-linking agents identified in the literature include glyoxal, glutaraldehyde, dialdehyde starch, dialdehyde chitosan, and the EDC/NHS mixture. Additionally, the review briefly discusses materials cross-linked with the MES/EDC mixture, caffeic acid, tannic acid, and genipin. Through a critical analysis of current research, this work aims to guide the development of more effective and safer biopolymeric materials tailored for biomedical applications, highlighting potential areas for further investigation and optimization. [ABSTRACT FROM AUTHOR]

Creating cross‐linking to establish efficient inter‐chain charge‐transfer channels in carbon nitride represents a promising strategy for enhancing its photocatalytic capabilities. Molten salt‐assisted calcining has emerged as a method for preparing cross‐linked carbon nitrides. However, the precise influence of molten salts on the molecular structure of carbon nitride remains to be fully elucidated. Herein, we develop a KCl guided cross‐linking reaction to preliminarily reveal the formation mechanism of cross‐linking. The cross‐linking reaction is initiated by the pre‐coordination of amino groups with K+. Subsequent heating at high temperature converts the amino groups into chlorines. Then, dechlorination leads to the formation of cross‐linking. Thus, this cross‐linking reaction can be accurately described as a pre‐coordination‐induced, two‐step deamination reaction. The pre‐coordination step plays a pivotal role in the cross‐linking process. Sufficient pre‐coordination results in a relatively high cross‐linking degree of the as‐prepared CNK‐2. Consequently, CNK‐2 demonstrates a significantly enhanced photocatalytic H2O2 production, with a generation rate of 682 μmol L−1 h−1, about 59 times that of traditional carbon nitride. [ABSTRACT FROM AUTHOR]

Starch is widely utilized in the food industry, but its native form may have limitations in terms of functionality and nutrition. This study examines the characteristics of native oat starch and explores its potential for chemical modification by cross‐linking, with the aim of gaining a deeper understanding of its functionality. Citrate‐modified oat starch (COS) is generated by cross‐linking native oat starch (NOS) with citric acid. Chemical analysis reveals distinctions between NOS and COS, notably in terms of resistant starch content, which is elevated in COS. X‐ray diffraction (XRD) results reveal that NOS exhibits crystalline peaks characteristic of A‐type starch, distinguishing it from COS. In contrast, COS displays absent crystalline peaks, attributed to cross‐linking. Swelling factor, solubility, and paste clarity along with most of the pasting properties are found to be significantly lower for COS compared to NOS. The scanning electron microscopic images show how cross‐linking can alter the morphology of the NOS. The findings from this investigation highlight significant distinctions between NOS and COS. The cross‐linking process successfully enhances the resistant starch content and imparted distinctive properties absent in native oat starch. Consequently, there is potential for incorporating modified oat starch as a food ingredient. [ABSTRACT FROM AUTHOR]

A series of triphenol‐diamine‐type hyperbranched benzoxazines are synthesized by using polyformaldehyde, 1,1,1‐tri(4‐hydroxyphenyl) ethane, and primary amines such as p‐phenylenediamine, 4,4′‐diaminodiphenylmethane, polyetheramine, and bifuranocyclic diamine via Mannich condensation. Then, copolymers with bifunctional benzoxazine (BA‐a) are prepared to obtain superior properties. The polymerization behavior of the copolymers examined using a differential scanning calorimeter and a Fourier transform infrared indicates that the introduction of hyperbranched benzoxazines facilitates the benzoxazine curing reaction, decreasing the onset and peak temperatures of the curing process. Thermogravimetric analysis results suggest the cured hyperbranched benzoxazine demonstrates good thermal stability and can improve the heat resistance of benzoxazine. In addition, dynamic mechanical analysis suggests the glass transition temperature of the copolymers with BA‐a was increased after copolymerization, thus making all the copolymers obtain higher service temperatures. The test results from the universal testing machine and the fracture morphologies of copolymers indicate the hyperbranched benzoxazines with branched structures cause dendritic folds to appear on the surface of copolymers upon polymerization, preventing rapid cracking and spreading of the thermoset resin by dissipating more impact energy through this irregular dendritic appearance, thus obtaining strength and toughness superior to that of BA‐a resins. [ABSTRACT FROM AUTHOR]

In this case series, we will describe sterile keratitis in the early postoperative period after hypotonic collagen cross-linking (CXL) in two pediatric cases. This is a retrospective case series of two eyes of two children who developed inflammatory keratitis with central corneal haze after uneventful epithelial-off hypotonic CXL. After ensuring microbiological sterility, appropriate treatment with topical steroids and lubricants was started. There was complete resolution of corneal infiltrates with minimal scarring. Both patients regained almost the preoperative best-corrected visual acuity of 20/80 and 20/60, respectively. [ABSTRACT FROM AUTHOR]

Tunable hydrogels have gained significant attention in the bioengineering field due to their designer preparation approach. Towards this end, gelatine stands out as a promising candidate owing to its desirable attributes, such as biocompatibility, ability to support cell adhesion and proliferation, biodegradability, and cost-effectiveness. This study presents the preparation of a robust gelatine hydrogel employing sacran aldehyde (SDA) as a natural cross-linker. The resulting SDA-cross-linked gelatine hydrogels (GSDA) display an optimal compressive stress of 0.15 MPa at 50% strain, five times higher than pure gelatine hydrogel. As SDA cross-linking concentration is increased, the swelling capacity of GSDA declines. This decline in swelling capacity, from 80% to 40%, is a result of strong crosslinking of gelatin with SDA. Probing further with FT-IR spectroscopy and SEM at the micron scale unveiled a dual-cross-linking mechanism within the hydrogels. This mechanism encompasses both short- and long-range covalent cross-linking, along with thermo-induced physical cross-linking, resulting in a significant enhancement of the load-bearing capacity of the fabricated hydrogels. [ABSTRACT FROM AUTHOR]

To examine functional, morphological, pasting, and digestibility properties, native bagana starch is subjected to physical, chemical, and dual modification respectively through heat moisture treatment, crosslinking, and combination of heat moisture and crosslinking. Accordingly, all modified starches except cross‐linked starch has showed higher solubility (heat moisture treated [23.33–27.33%] and heat moisture‐cross‐linked [21.33–26%]) and lower swelling power (2.07–3.83 g g−1) and (2.22–3.86 g g−1) respectively than native bagana starch (16.33–25%) and (2.03–6.82 g g−1). Heat moisture treated and cross‐linked starches have showed similar morphology with native starch. The lower breakdown and setback viscosities for cross‐linked starch (68.67 and 182 cp) and heat moisture‐cross‐linked starches (38.67 and 194.67 cp) have resulted in adequate capability for good shear resistance and anti‐retrogradation properties than same viscosities of native starch (126.67 and 770 cp). The in vitro digestibility of dual modified starch has resulted in good resistant starch content (26.40%) than native bagana (17.89%), heat moisture treated (15.68%), and cross‐linked (24.93%) starches. The study reveals dual modification using heat moisture and cross‐linking is an effective method to improve the physicochemical and thermal properties of starch and can advantageously result in a good resistant starch content, which is the most emphasized health issue; thus, attention should be given to broaden its application in the food industry. [ABSTRACT FROM AUTHOR]

The combustion of fuel with high sulfur concentrations produces a large number of sulfur oxides (SOx), which have a range of negative effects on human health and life. The preparation of catalysts with excellent performance in the oxidative desulfurization (ODS) process is highly effective for reducing SOx production. In this paper, cross-linked polyvinylimidazole (VE) was successfully created using a simple ontology aggregation method, after which a catalyst of polyvinylimidazolyl heteropolyacid clusters (VE-HPA) was prepared by adding heteropolyacid clusters. Polyvinylimidazolyl-phosphotungstic acid (VE-HPW) showed an outstanding desulfurization performance, and the desulfurization efficiency reached 99.68% in 60 min at 50 °C with H2O2 as an oxidant. Additionally, the catalyst exhibited recyclability nine consecutive times and remained stable, with a removal rate of 98.60%. The reaction mechanism was eventually proposed with the assistance of the free radical capture experiment and GC-MS analysis. [ABSTRACT FROM AUTHOR]

Effective enzyme stabilization through immobilization is essential for the functional usage of enzymatic reactions. We propose a new method for synthesizing elastic hydroxyapatite microgel (E-HAp-M) materials and immobilizing lipase using this mesoporous mineral via the ship-in-a-bottle-neck strategy. The physicochemical parameters of E-HAp-M were thoroughly studied, revealing that E-HAp-M provides efficient space for enzyme immobilization. As a model enzyme, lipase (LP) was entrapped and then cross-linked enzyme structure, preventing leaching from mesopores, resulting in highly active and stable LP/E-HAp-M composites. By comparing LP activity under different temperature and pH conditions, it was observed that the cross-linked LP exhibited improved thermal stability and pH resistance compared to the free enzyme. In addition, they demonstrated a 156% increase in catalytic activity compared with free LP in hydrolysis reactions at room temperature. The immobilized LP maintained 45% of its initial activity after 10 cycles of recycling and remained stable for over 160 days. This report presents the first demonstration of a stabilized cross-linked LP in E-HAp-M, suggesting its potential application in enzyme-catalyzed processes within biocatalysis technology. [ABSTRACT FROM AUTHOR]

Many stimuli‐responsive materials harness the reversible association of supramolecular binding motifs to enable advanced functionalities such as self‐healing, switchable adhesion, or mechanical adaptation. Despite extensive research into the structure–property relationships of these materials, direct correlations between molecular‐level changes in supramolecular binding and macroscopic material behaviors have mostly remained elusive. Here, we show that this challenge can be overcome with supramolecular binding motifs featuring integrated binding indicators. We demonstrate this using a novel motif that combines a hydrogen‐bonding ureido‐4‐pyrimidinone (UPy) with two strategically placed pyrene fluorophores. Dimerization of this motif promotes pyrene excimer formation, facilitating the straightforward optical quantification of supramolecular assembly under various conditions. We exploit the new motif as a supramolecular cross‐linker in poly(methyl acrylate)s to probe the extent of (dis)assembly as a function of cross‐linker content, processing history, and applied stimuli. We demonstrate that the stimuli‐induced dissociation of hydrogen‐bonding linkages strongly depends on the initial cross‐link density, which also dictates whether the force‐induced dissociation in polymer films correlates with the applied stress or strain. Thus, beyond introducing a robust tool for the in situ study of dynamic (dis)assembly mechanisms in supramolecular systems, our findings provide new insights into the mechanoresponsive behavior of such materials. [ABSTRACT FROM AUTHOR]

Introduction: Equipped with a photosynthetic apparatus that uses the energy of solar radiation to fuel biosynthesis of organic compounds, chloroplasts are the metabolic factories of mature leaf cells. The first steps of energy conversion are catalyzed by a collection of protein complexes, which can dynamically interact with each other for optimizing metabolic efficiency under changing environmental conditions. Materials and methods: For a deeper insight into the organization of protein assemblies and their roles in chloroplast adaption to changing environmental conditions, an improved complexome profiling protocol employing a MS- cleavable cross-linker is used to stabilize labile protein assemblies during the organelle isolation procedure. Results and discussion: Changes in protein:protein interaction patterns of chloroplast proteins in response to four different light intensities are reported. High molecular mass assemblies of central chloroplast electron transfer chain components as well as the PSII repair machinery react to different light intensities. In addition, the chloroplast encoded RNA-polymerase complex was found to migrate at a molecular mass of -8 MDa, well above its previously reported molecular mass. Complexome profiling data produced during the course of this study can be interrogated by interested readers via a web-based online resource (https://complexomemap.de/projectsinteraction-chloroplasts). [ABSTRACT FROM AUTHOR]

In this work, microcapsules were developed by the complex coacervation of sodium caseinate and pectin as a carrier for saffron extract. Parameters such as Zeta potential, dynamic light scattering, and microscopic techniques were investigated for their influence on the formation of these complexes. Furthermore, Fourier transform infrared (FTIR) analysis confirmed the reaction mechanism between the protein and tannic acid or saffron extract. The study revealed that core/shell and protein/polysaccharide (Pr/Ps) ratios play a role in the encapsulation efficiency (EE) and loading capacity (LC) of saffron extract, with EE and LC ranging from 48.36 to 89.38% and 1.14 to 5.55%, respectively. Thermal gravimetric analysis revealed that the degradation temperature of saffron increased significantly with microencapsulation. The use of tannic acid for hardening the microcapsules led to an increase in size from 13 μm to 27 μm. Rheological findings indicated that shear-thinning behavior in the coacervates, with cross-linking, has a minor effect on the interconnected elastic gel structures. However, cross-linking improved the microcapsules' thermal and structural properties. The increase in polymer chain length due to cross-linking and the presence of the guest molecule (saffron extract) resulted in higher rheological moduli, reflecting enhanced entanglements and correlating well with the thermal, structural, and microstructural properties of the coacervates. Kinetic release studies showed a slower release in the gastric phase compared to the intestinal phase, with the Ritger–Peppas model effectively describing saffron extract release, highlighting a dominant swelling and dissolution release mechanism. Therefore, the NaCas/HMP coacervate wall materials made saffron stable in the gastric stage and sustainably release. It in the intestinal stage, promoting excellent absorption of saffron in simulated digestion. [ABSTRACT FROM AUTHOR]

AbstractSelf-healing materials have garnered significant attention for their potential to heal damage when it occurs. Elastomers, particularly natural rubber, have been a focal point of extensive research in the realm of self-healing materials. The ability of self-healing in natural rubber not only promises to extend the service life of rubber-based products but also offers new avenues for recyclability and reprocessability, contributing to environmental protection efforts. A key challenge in the self-healing of natural rubber has been to enhance its self-healing capabilities without compromising its mechanical properties. As a result, various self-healing mechanisms such as hydrogen bond, Diels–Alder (D-A) reaction, disulfide bond, imine bond, and ionic bond have been thoroughly investigated. Among these mechanisms, reversible ionic bonds or ionic interactions have emerged as particularly influential in facilitating the self-healing of natural rubber. This mechanism is easily incorporated into the structure of natural rubber due to its high stability, enabling natural rubber to exhibit promising self-healing properties. This review delves into a comprehensive statistical analysis of numerous published articles and focuses on the exploration of the ionic bonding mechanism in the context of self-healing in natural rubber. Additionally, it provides a succinct introduction to specialized tests designed to assess the self-healing in natural rubber focusing on related methods for ionic bonds mechanism evaluation, namely swelling test and healing efficiency test. [ABSTRACT FROM AUTHOR]

Serial capture affinity purification (SCAP) is a powerful method to isolate a specific protein complex. When combined with cross-linking mass spectrometry and computational approaches, one can build an integrated structural model of the isolated complex. Here, we applied SCAP to dissect a subpopulation of WDR76 in complex with SPIN1, a histone reader that recognizes trimethylated histone H3 lysine4 (H3K4me3). In contrast to a previous SCAP analysis of the SPIN1:SPINDOC complex, histones and the H3K4me3 mark were enriched with the WDR76:SPIN1 complex. Next, interaction network analysis of copurifying proteins and microscopy analysis revealed a potential role of the WDR76:SPIN1 complex in the DNA damage response. Since we detected 149 pairs of cross-links between WDR76, SPIN1, and histones, we then built an integrated structural model of the complex where SPIN1 recognized the H3K4me3 epigenetic mark while interacting with WDR76. Finally, we used the powerful Bayesian Integrative Modeling approach as implemented in the Integrative Modeling Platform to build a model of WDR76 and SPIN1 bound to the nucleosome. [ABSTRACT FROM AUTHOR]

Waste from non-degradable packaging materials poses a serious environmental risk and has led to interest in developing sustainable bio-based packaging materials. Sustainable packaging materials have been made from diverse naturally derived materials such as bamboo, sugarcane, and corn starch. In this study, we made a sustainable packaging film using chitosan extracted from the biomass of yellow mealworm (Tenebrio molitor) shell waste. The extracted chitosan was used to create films, cross-linked with citric acid (CA) and with the addition of glycerol to impart flexibility, using the solvent casting method. The successful cross-linking was evaluated using Fourier-Transform Infrared (FTIR) analysis. The CA cross-linked mealworm chitosan (CAMC) films exhibited improved water resistance with moisture content reduced from 19.9 to 14.5%. Improved barrier properties were also noted, with a 28.7% and 10.2% decrease in vapor permeability and vapor transmission rate, respectively. Bananas were selected for food preservation, and significant changes were observed over a duration of 10 days. Compared to the control sample, bananas packaged in CAMC pouches exhibited a lesser loss in weight because of excellent barrier properties against water vapor. Moreover, the quality and texture of bananas packaged in CAMC pouch remained intact over the duration of the experiment. This indicates that adding citric acid and glycerol to the chitosan structure holds promise for effective food wrapping and contributes to the enhancement of banana shelf life. Through this study, we concluded that chitosan film derived from mealworm biomass has potential as a valuable resource for sustainable packaging solutions, promoting the adoption of environmentally friendly practices in the food industry. [ABSTRACT FROM AUTHOR]

The utilization of biodegradable hydrogels based on natural polysaccharides in the agricultural and biomedical sectors is anticipated to be a growing field of interest. Due to increasing environmental pollution, the current global goal is to synthesize sustainable materials based on natural polysaccharides to conserve natural resources for the future. In this study, we synthesized an amla-based hydrogel, denoted as AL-g-poly(MAA), using the graft-free radical polymerization method. Methacrylic acid (MAA) was employed as the monomer, N,N′-methylenebisacrylamide (MBA) served as the crosslinker, and ammonium persulfate (APS) acted as the initiator. The synthesized hydrogel, AL-g-poly(MAA), underwent optimization by adjusting seven parameters: initiator, solvent, time, monomer, power, pH, and crosslinker, to achieve the highest swelling percentage. The optimized values were as follows: solvent: 10 ml, time: 150 s, monomer: 0.039 mol/L, power: 60%, pH: 7, and crosslinker: 0.0648 mol/L. The cross-linking process was confirmed through Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and thermal gravimetric analysis (TGA) techniques. The swelling behavior of the synthesized hydrogels was determined in saline solutions with varying ionic strengths and concentrations, revealing maximum swelling in solutions with lower ionic strengths and concentrations. Additionally, the density and porosity of the hydrogels were examined. The biodegradability of AL-g-poly(MAA) was tested through soil burial and vermicomposting experiments, demonstrating its significant potential for agriculture applications. Furthermore, both the backbone and the synthesized hydrogel were evaluated for antibacterial activity against four bacterial strains (Burkholderia gladioli, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus cereus), revealing strong potential as an antimicrobial agent and therefore having applications in the biomedical field. The mechanism underlying the inhibitory effect of synthesized AL-g-poly(MAA) hydrogel on bacterial cell membranes is also discussed. [ABSTRACT FROM AUTHOR]

This study explored the changes in cross-linking of low-salt myosin mediated by microbial transglutaminase (MTGase) under high intensity ultrasound (HIU). HIU activated the fish endogenous transglutaminase by 14.11%. Meanwhile, HIU induced the conformational changes in low-salt myosin with decrease of α-helix and increase of β-sheet structures. At 0.1 mol/L salt, compared to solely treated MTGase/solely treated myosin, the most ε-(γ-Glu)-Lys bonds were formed in HIU-treated MTGase + myosin, evidenced by the lowest solubility. Correspondingly, the G' showed the highest increase rate. Consequently, the samples formed regular and continuous protein matrix structures. Specifically, the microstructures of HIU-treated MTGase + myosin samples at 0.1 mol/L salt were even more compact than those of control samples at 0.3 mol/L salt. Besides, HIU-treated MTGase + myosin improved the water holding capacity by 18.28%. In summary, HIU promoted the cross-linking between low-salt myosin mediated by MTGase through activating the enzyme, improving substrate dispersion, or both, with the largest improvement degree observed for HIU-treated MTGase + myosin group. [ABSTRACT FROM AUTHOR]

Purpose: The aim of the study was to determine the effects of corneal collagen cross-linking (CXL) on tear function parameters in a long-term period retrospectively. Methods: Twenty-four eyes of 17 keratoconus patients after CXL treatment were included in the study. The ocular surface disease index questionnaire (OSDI), tear osmolarity, tear break-up time (T-BUT), Oxford ocular surface staining score, Schirmer I test, and the National Eye Institute Visual Function Questionnaire-25 were performed before and after CXL at 1st and 24th months. All parameters were compared. Results: Tear osmolarity significantly increased during follow-up (p=0.001). The increment in T-BUT was significant between pre-operative and 1st month (p=0.001). Oxford grading score increased progressively but the difference was only significant between pre-operative and 24 months (p<0.05). Schirmer's score improved at 1st month but altered in favor of dry eye at 24 months similar to T-BUT. OSDI and tear osmolarity were significantly increased in all visits (p<0.05). Conclusion: Dry eye disorder was demonstrated as a significant complication of CXL in keratoconic eyes in a long-term period. Even if we performed CXL at early times, we need to follow patients for ocular surface disorders as well as topographic progression for the period of long time because the side effects of CXL on the ocular surface last up to 24 months. [ABSTRACT FROM AUTHOR]

Melt blending is a reliable and well‐demonstrated strategy for improving the mechanical, thermal, rheological, and surface properties of biopolymers. Poly(hydroxy‐3‐butyrate‐co‐3‐hydroxyvalerate) (PHBV) and poly(butylene adipate‐co‐terephthalate) (PBAT) are the two popular choices for blending polymers due to their diverse properties and complementary soil biodegradable behaviour. Due to their immiscibility, however, blending with the help of processing additives is necessary to reap the most significant benefits from this process and to avoid immiscibility issues. This study utilized the additives (peroxides and epoxy‐based chain extender) to compatibilize the biodegradable polymers PHBV and PBAT in a 60:40 blending ratio. The tensile strength and Young's modulus of the PHBV/PBAT(60/40) blend were improved by 32% and 64%, respectively, after adding a combination of peroxide (0.02 phr) and chain extender (0.3 phr) due to the formation of a complex network structure with increased chain length. The positive effect of an additive addition was also reflected by a 30°C increment in heat deflection temperature of biodegradable blend due to its high modulus value as supported by mechanical properties. The combined action of a peroxide and chain extender demonstrated a significantly higher complex viscosity of the PHBV/PBAT(60/40) blend due to the formation of a crosslinked polymer network as analyzed by rheological analysis. Our research demonstrated the effect of additives and their combined impact on analytical properties of PHBV/PBAT(60/40) blend to guide future work in improving their candidature to serve as a drop‐in solution in replacing non‐biodegradable petro‐based plastic products. [ABSTRACT FROM AUTHOR]

Polymer‐based membrane technology holds immense promise for CO2 separation. However, it faces persistent challenges, including the high CO2 pressure‐induced plasticization and permeability‐selectivity trade‐offs, which significantly hinder the development of polymeric membranes. To tackle this issue, we synthesized a novel polyimide 6FDA‐DAT:DABA(6FDD) containing triptycene and carboxylic groups. Upon de‐carboxylation induced cross‐linking, the membrane demonstrated a simultaneous enhancement of gas permeability and selectivity. Specifically, compared to the uncross‐linked 6FDD, the 400°C‐24 h cross‐linked membrane exhibited a remarkable increase in CO2 permeability by 177% (93.1 Barrer) and a significant rise in CO2/CH4 selectivity by 47% (57.5), reaching the CO2/CH4 upper bound. More importantly, the cross‐linked membrane displayed vastly improved CO2 plasticization resistance, withstanding up to 42 bar of CO2 feed pressure. The design of decarboxylated cross‐linked membranes in this work paves the way for creating high‐performing and plasticization‐resistant membranes with potential applications in high‐pressure CO2 separations. [ABSTRACT FROM AUTHOR]

Isobam is widely used for fabricating ceramics through spontaneous gelation and has attracted considerable interest. However, the disadvantage of the Isobam system is the low gelation strength. The effects of suitable additives and the mechanism by which they effectively enhance the green body strength and the rheological behavior of an aluminum nitride (AlN) slurry with 50 vol% solid loading were investigated using polyethyleneimine (PEI), hydantoin epoxy resin, and trimethylolpropane triglycidyl ether (TMPGE). Results showed that the additives acted as both dispersants and cross-linkers in the AlN suspension using the Isobam gelling system. The flexural strength of the AlN green body increased by 42%, 204%, and 268% with the addition of 1 wt% PEI, 1 wt% hydantoin epoxy resin, and 0.5 wt% TMPGE, respectively. After sintering at 1700 °C, the AlN ceramic with 0.5 wt% TMPGE had flexural strength and thermal conductivity of 235 MPa and 166.44 W/(m·K), respectively, showing superior performance to the ceramics without additives. [ABSTRACT FROM AUTHOR]

Electrospinning is a widely employed manufacturing platform for tissue engineering applications because it produces structures that closely mimic the extracellular matrix. Herein, we demonstrate the potential of poly(vinyl alcohol) (PVA) electrospun nanofibers as scaffolds for tissue engineering. Nanofibers were created by needleless direct current electrospinning from PVA with two different degrees of hydrolysis (DH), namely 98% and 99% and subsequently heat treated at 180 °C for up to 16 h to render them insoluble in aqueous environments without the use of toxic cross-linking agents. Despite the small differences in the PVA chemical structure, the changes in the material properties were substantial. The higher degree of hydrolysis resulted in non-woven supports with thinner fibres (285 ± 81 nm c.f. 399 ± 153 nm) that were mechanically stronger by 62% (±11%) and almost twice as more crystalline than those from 98% hydrolysed PVA. Although prolonged heat treatment (16 h) did not influence fibre morphology, it reduced the crystallinity and tensile strength for both sets of materials. All samples demonstrated a lack or very low degree of haemolysis (<5%), and there were no notable changes in their anticoagulant activity (≤3%). Thrombus formation, on the other hand, increased by 82% (±18%) for the 98% hydrolysed samples and by 71% (±10%) for the 99% hydrolysed samples, with heat treatment up to 16 h, as a direct consequence of the preservation of the fibrous morphology. 3T3 mouse fibroblasts showed the best proliferation on scaffolds that were thermally stabilised for 4 and 8 h. Overall these scaffolds show potential as 'greener' alternatives to other electrospun tissue engineering materials, especially in cases where they may be used as delivery vectors for heat tolerant additives. [ABSTRACT FROM AUTHOR]