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Biobased hydrogels have been widely used in drug delivery, tissue engineering and biosensors due to their abundance, non-toxicity and biocompatibility. However, constructing fully biobased hydrogels with good mechanical performance still remains a challenge. Herein, a double network (DN) hydrogel consisting of oxidized hydroxypropyl guar gum (OHPG) and gelatin (Gel) was fabricated via Schiff base reaction. The Gel-OHPG hydrogel had an elongation at break of 497%, a tensile stress of 0.44 MPa and a compressive stress of 25.91 MPa. Then, the mechanical properties of the hydrogel were further enhanced through immersing it in an ammonium sulfate (AMS) solution due to the Hofmeister effect. Its elongation could reach 629% and the corresponding tensile toughness and compressive stress were 3.86 MPa and 59.55 MPa, respectively. The conductivity of the hydrogel was 0.86 S m−1. Furthermore, the Gel-OHPG hydrogel was fabricated as a flexible sensor, and it could accurately monitor human joint motions such as fingers, wrists, knees, elbows, throat and neck. Henceforth, the Gel-OHPG hydrogel prepared using fully natural polymers has promising potential in flexible sensors and tissue engineering. [ABSTRACT FROM AUTHOR]

Recent advancements in tissue engineering have witnessed luffa-derived scaffolds, exhibiting their exceptional potential in cellular proliferation, biocompatibility, appropriate interconnectivity, and biomechanical strength. In vivo studies involved implanting fabricated scaffolds subcutaneously in Wistar rats to evaluate their impact on the heart, liver, and kidneys. This approach provided a safe and minimally invasive means to evaluate scaffold compatibility with surrounding tissues. Male Wistar rats were categorized into four distinct groups, Group A, B, C, and D are referred to as 3% LC implanted scaffolds, 5% LC implanted scaffolds, control (without luffa scaffolds), and Sham (without any scaffold implantation), respectively. Histological analysis in all the groups indicated that the animal models did not exhibit any signs of inflammation or toxicity, suggesting favorable tissue response to the implanted scaffolds. Initial observations revealed elevated levels of enzymes and biomarkers in the experimental groups after a 24 h interval, including aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), bilirubin, creatine kinase-MB (CK-MB), and serum creatinine. However, these parameters normalized 3 weeks post-implantation, with no significant increase compared to the control groups, suggesting that the implanted luffa-based scaffolds did not induce adverse effects on the heart, liver, and kidneys. Furthermore, the scaffold's significant pore size and porosity enable it to release drugs, including antibacterial medications. This study demonstrates promising results, indicating excellent scaffold porosity, sustained drug release, affirming the in vivo biocompatibility, absence of inflammatory responses, and overall tissue compatibility highlighting the immense potential of these luffa-based scaffolds in various tissue engineering and regenerative medicine applications. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Food & Fermentation Industries is the property of Food & Fermentation Industries and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Shipin Kexue/ Food Science is the property of Food Science Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

There is an ongoing effort to advance methodologies for culturing functional photoreceptors in vitro for retinal regenerative strategies. To support the formation of functional photoreceptors, a scaffold should replicate the native environment. The aim of this study was to optimize a sodium alginate–gelatin (SA-G) bioink to mimic the retinal properties while ensuring the printing of constructs with high shape fidelity. The optimized bioink was thoroughly characterized in terms of its physical, mechanical, and rheological properties, printability assessment, and preliminary biocompatibility. The material showed a constant degradation rate, which is crucial for effective tissue regeneration as it provides support for cell differentiation and polarization while gradually degrading to allow cell proliferation and matrix deposition. The optimized bioink displayed stiffness comparable to the native photoreceptor layer, potentially providing appropriate mechanical cues for photoreceptor maturation. Additionally, it exhibited shear-thinning behavior, the presence of yield stress, and fast recovery kinetics, which are essential for successful extrusion. The high shape fidelity of 3D-printed constructs suggested the feasibility of printing complex patterns to drive photoreceptor polarization. The preliminary cell results demonstrated homogeneous cell distribution and sustained cell viability over time. Overall, these findings indicate that the optimized bioink can provide the mechanical and topographical cues necessary for cultivating photoreceptors in vitro for retinal regeneration. [ABSTRACT FROM AUTHOR]

The defensive tissues such as insect epidermis and crustacean exoskeleton in nature displayed characteristics of high strength and high toughness via multi‐level structure, which shed light on the designation of natural polymer‐based composites with enhanced mechanical property. Herein, a bioinspired strategy was used to prepare chitin/gelatin composite with improved mechanical property. Chitin hydrogels were first prepared by dissolution in NaOH/urea via freezing–thawing and then regeneration in sodium propionate, to form a heterogeneous nanofibrous structure. After coating gelatin on the chitin nanofibers, a hierarchical structure was obtained, leading to more compact and homogenous morphology. The coating process significantly strengthened the chitin nanofibrous structure and reduced the weak defect, which enhanced the tensile strength and toughness of the composite. The present work not only supplies a chitin/gelatin composite with high mechanical property but also offers a facile approach to prepare strengthening and toughening materials based on natural polymers. [ABSTRACT FROM AUTHOR]

To investigate the effect of the interaction between protocatechuic acid (PCA) and gelatin on the functional properties and stability of gelatin-PCA complexes. Gelatin-PCA complexes were prepared by non-covalent and covalent binding. Afterward, the interaction between PCA and gelatin was analyzed using UV-Vis spectroscopy, fluorescence spectroscopy, and Fourier transform infrared spectroscopy. Meanwhile, an analysis was also performed on the antioxidant activity, antibacterial activity, and stability of the complexes. The findings showed a higher PCA binding rate for the covalent complexes than the non-covalent complexes. Additionally, the interaction between PCA and gelatin resulted in the fluorescence quenching of gelatin, with a higher level of fluorescence quenching observed for the covalent binding. Moreover, in addition to excellent DPPH and ABTS+ radical scavenging abilities. Compared with GPCA-2, the noncovalent complex GPCA-1 showed more significant (P<0.05) scavenging abilities against DPPH and ABTS+ free radicals, with clearance rates of 49.71%±2.9% and 38.39%±0.57%, respectively. Gelatin-PCA complexes also exhibited antibacterial activity against Escherichia coli, Listeria monocytogenes, and Salmonella. Moreover, the antibacterial effect of GPCA-1 was more significant (P<0.05), with inhibition zone diameters of 11.31±0.91, 12.57±0.93 and 8.83±0.35 mm for E. coli, L. monocytogenes and Salmonella, respectively. Despite reducing the antioxidant and antibacterial activities of PCA to some extent, the interaction between PCA and gelatin significantly (P<0.05) improved the photostability and thermal stability of PCA. Specifically, the retention rates of PCA in gelatin-PCA covalent complexes after 80 min of UV and heat treatment were 92.58%±0.62% and 90.30%±0.97%, respectively. In conclusion, these findings provide a theoretical basis for the development and utilization of functional gelatin-PCA complex products. [ABSTRACT FROM AUTHOR]

Among hydrocolloids used in the food industry, gelatin (an animal protein) is remarkably known for its unique gel forming ability. Creating a perfect, green substitute for animal gelatin is extremely difficult if not impossible, because this versatile hydrocolloid offers many special properties that are not easily imitated by other vegetable-based systems. The combination of more than one type of hydrocolloid is commonly used in food either to bridge the above-mentioned gap or to impart novel organoleptic characteristics (such as mouthfeel) to food products, to modify rheological characteristics, and to satisfy processing requirements in the industry. In this work, we study the rheology and the texture of water mixtures of κ-Carrageenan (κ-C) and Locust Bean Gum (LBG). By fixing different κ-C concentrations and varying the LBG/κ-C ratio, we explore a wide range of potentially useful textures. The results obtained for the green systems are also compared to those exhibited by animal gelatin formulations. [ABSTRACT FROM AUTHOR]

We report a 12‐month‐old boy with a skin eruption that developed 15 days after receiving the measles, mumps, rubella (MMR), pneumococcal, and meningococcal vaccines, consistent with the diagnosis of Wells syndrome. Patch testing showed a positive reaction to gelatin, which is used as a stabilizer for both live and inactivated vaccines. Gelatin was only present in the MMR vaccine. [ABSTRACT FROM AUTHOR]

3D‐printed food exhibits unique advantages in precision nutrition food and personalized customization, achieving disease prevention and treatment through personalized nutrition plans and scientific addition. In this study, 3D‐printing and stable structure of gelatin‐based foods were achieved by heating extrusion. On this basis, we compared the relationship between gelatin viscosity and formability, quantified the water diffusion of composite hydrogels, and verified the edibility of each stage and component by gel strength test and texture profile analysis. The optimal content of the composite hydrogel was 35% gelatin and 5% glycerol, and the concentration of TG enzyme solution was 5%. On this basis, the content of brown sugar increased to 15% did not affect the 3D‐printing formability. Therefore, the 3D‐printed gelatin‐based composite hydrogels in this study provided a processing scheme for high adding nutrients to food 3D‐printed products. [ABSTRACT FROM AUTHOR]

The repair of bone defects has been the focus of research at home and abroad in recent years. Gelatin methacryloyl (GelMA) hydrogels, with their good biocompatibility, low cost, photo-cross-linking structure, and easily adjustable physicochemical property, have been widely used in bone regeneration. GelMA hydrogels can overcome issues such as inadequate mechanical property, poor bioactivity, and uncontrolled degradation through various strategies. This paper presents a systematic review of recent advances in GelMA hydrogels in the field of bone defect repair, covering the preparation of GelMA hydrogels and the effect of reaction conditions on the property, the loading and controlled release of GelMA hydrogels (drugs, cells, growth factors, exosomes), material hybridization (organic nanomaterials, inorganic nanomaterials, organic and inorganic hybrid materials) of GelMA hydrogels, structural modulation (electrostatic spinning, microspheres, 3D printing), as well as the mechanism of osteogenic activity (vascular, neural, immunomodulation) in bone defects. Finally, we summarized this article and looked forward to the prospects and challenges of GelMA hydrogel in repairing bone defects. [ABSTRACT FROM AUTHOR]

Ethmoid myoepithelial carcinoma is a rare tumor, with only 14 cases reported to date. This report discusses the largest tumor of this type ever recorded in the ethmoid region. The tumor caused extensive damage to facial structures, complicating treatment. The patient’s age and comorbidities increased the risk of intraoperative bleeding, presenting challenges to the complete removal of the tumor and the reconstruction of the damaged structures. To reduce the risk of intraoperative hemorrhage, shorten the surgery time, and manage potential heartrelated complications, arterial embolization was performed using gelatin sponges and coils. Definitive surgery was then carried out using a skin flap and mucosal flap to successfully reconstruct the defect. Postoperative radiotherapy was deemed unnecessary. The patient recovered well, with a satisfactory aesthetic outcome. No recurrence was observed during a 3-year follow-up period. [ABSTRACT FROM AUTHOR]

Gelatin-based aerogel (G-Aerogel) from untanned proteinaceous solid wastes was applied as an adsorbent in batch and fixed-bed column systems to remove acid red 97 (AR97) from water. Adsorption was evaluated as a function of pH, adsorbent mass, contact time, temperature, and initial dye concentration. Maximum removal of AR97 was achieved at pH 3 after about 4 h. The pseudo-second-order equation provided the best adsorption kinetic model. The adsorption of AR97 onto G-Aerogel was best described with the Langmuir model, and the maximum adsorption capacity was about 196 mg·g−1. A thermodynamic study showed an exothermic and spontaneous adsorption process. It was also demonstrated that G-Aerogel can be reused several times. The column study showed that breakthrough and saturation times decreased with increasing initial AR97 concentration. Thomas and Yoon-Nelson kinetic models were applied to the experimental data to predict the breakthrough curves and determine the characteristic parameters of column adsorption. Practical Applications: Tannery solid wastes composed mainly of collagen are very abundant and constitute a material that should be valorized. In this study, we examined the transformation of untanned proteinaceous wastes into a biomaterial [Gelatin-based aerogel (G-Aerogel)] of environmental interest. The results demonstrated the promise of this material for dye adsorption because of its advantages in terms of its ease of preparation, its containing functional groups that are able to attract dye, its ability to be reused several cycles, and its high adsorption capacity. In addition to studying adsorption in static mode, we also studied dynamic adsorption, because the common industrial practice is to pass water to be treated through a column packed with an adsorbent, allowing the transport of the pollutant from the liquid to the solid. In summary, G-Aerogel can be applied as an environmentally friendly and efficient adsorbent for the removal of dyes from contaminated water. [ABSTRACT FROM AUTHOR]

In this study, polyethylene glycol (PEG), as a sacrificial agent, and gelatin containing graphene oxide (GO) are co-electrospun to prepare scaffolds. Based on pore size measurements, removal of PEG leads to an increase in the pore size of modified scaffolds, resulting in easier infiltration. Moreover, noticeable elastic modulus of GO increased the mechanical strength. Alizarin red staining indicated proliferation and differentiation of human bone marrow-derived mesenchymal stem cells seeded on the modified scaffolds. Thus, gelatin scaffold containing 0.5% GO with 20% PEG at the ratio of 80:20 for gelatin–PEG was selected as the optimal scaffold for bone tissue engineering approaches. [ABSTRACT FROM AUTHOR]

Summary: Potato flour/gelatine films in different ratios (6:0, 5:1, 4:1, 3:1, 2:1 and 1:1) were prepared and their properties were examined in this study. Potato flour film‐forming dispersion without gelatine showed the highest particle size and apparent viscosity. As the gelatine concentration increased, the composite films became smoother and more transparent. Gelatine incorporated with potato flour films reduced the retrogradation enthalpy and glass transition temperature, leading to the low tensile strength and high elongation at break. Although water content and water solubility index increased with the higher gelatine concentration, water vapour permeability of composite films decreased from 14.59 × 10−13 gm−1s−1Pa−1 to 5.83 × 10−13 gm−1s−1Pa−1. In addition, it was noted that water contact angle increased from 24.50° to 102.33° as gelatine concentration increased from 0% (6:0) to 50% (1:1). According to these findings, potato flour film with the presence of gelatine showed the better moisture barrier properties. [ABSTRACT FROM AUTHOR]

pH-responsive hydrogels have numerous applications in tissue engineering, drug delivery systems, and diagnostics. Gelatin methacryloyl (GelMA) is a biocompatible, semi-synthetic polymer prepared from gelatin. When combined with aqueous solvents, GelMA forms hydrogels that have extensive applications in biomedical engineering. GelMA can be produced with different degrees of methacryloyl substitution; however, the synthesis of this polymer has not been tuned towards producing selectively modified materials for single-component pH-responsive hydrogels. In this work, we have explored two different synthetic routes targeting different gelatin functional groups (amine, hydroxyl, and/or carboxyl) to produce two GelMA analogs: gelatin A methacryloyl glycerylester (polymer A) and gelatin B methacrylamide (polymer B). Polymers A and B were used to fabricate pH-responsive hydrogel microspheres in a flow-focusing microfluidic device. At neutral pH, polymer A and B microspheres displayed an average diameter of ~40 µm. At pH 6, microspheres from polymer A showed a swelling ratio of 159.1 ± 11.5%, while at pH 10, a 288.6 ± 11.6% swelling ratio was recorded for polymer B particles. [ABSTRACT FROM AUTHOR]

TiO2 material has an important position in the processing of methylene blue waste because it is economical, has abundant polymorphs, high sustainability and supports green chemistry applications. Mesoporous TiO2 is a porous material that has higher effectiveness than other TiO2 because the pore structure has a large diameter at the nano scale (2-50 nm) with a regular shape so that the surface area and pore volume are greater than the average for other TiO2. The synthesis of mesopore TiO2 material has so far used the sol-gel route with synthetic pore directing agents such as P123 which can be replaced with gelatin as a cheaper and safer pore directing agent with high sustainability and abundance. Based on the description above, this research aims to photodegrade methylene blue using mesoporous TiO2 (m-TiO2) nanoparticles which were prepared by the sol-gel method using gelatin and P123 as template. X-ray diffraction (XRD), scanning electron microscopy (SEM), Electron dispersive X-Ray (EDX), and UV-vis spectroscopy techniques were used to characterize the samples. Photocatalytic activities of samples for methylene blue degradation were investigated. The catalyst before and after regeneration will be studied so that the effect of regeneration on the results of methylene blue photocatalysis with m-TiO2 can be determined. XRD results confirmed the formation of the anatase and rutile phase for the TiO2 nanoparticles, with crystallite sizes larger after regeneration in the range of 9-21 nm. The large particle size was after regeneration due to the promotion by high temperature treatment. TiO2 nanoparticles showed the best photocatalytic activity on the first use to 91% and remained stable after four cycles with photodegradation efficiency up to 76% based on the measured UV-Vis spectroscopy. TiO2 as synthesis could be the best candidate for catalyst with the high performance after multicycle regeneration. [ABSTRACT FROM AUTHOR]

The secreted aspartic peptidases (Saps) of Candida albicans play crucial roles in various steps of fungal–host interactions. Using a flow cytometry approach, this study investigated the expression of Saps1–3 antigens after (i) incubation with soluble proteins, (ii) interaction with mammalian cells, and (iii) infection in immunosuppressed BALB/c mice. Supplementation strategies involving increasing concentrations of bovine serum albumin (BSA) added to yeast carbon base (YCB) medium as the sole nitrogenous source revealed a positive and significant correlation between BSA concentration and both the growth rate and the percentage of fluorescent cells (%FC) labeled with anti-Saps1–3 antibodies. Supplementing the YCB medium with various soluble proteins significantly modulated the expression of Saps1–3 antigens in C. albicans. Specifically, immunoglobulin G, gelatin, and total bovine/human sera significantly reduced the %FC, while laminin, human serum albumin, fibrinogen, hemoglobin, and mucin considerably increased the %FC compared to BSA. Furthermore, co-cultivating C. albicans yeasts with either live epithelial or macrophage cells induced the expression of Saps1–3 antigens in 78% (mean fluorescence intensity [MFI] = 152.1) and 82.7% (MFI = 178.2) of the yeast cells, respectively, compared to BSA, which resulted in 29.3% fluorescent cells (MFI = 50.9). Lastly, the yeasts recovered from the kidneys of infected immunosuppressed mice demonstrated a 4.8-fold increase in the production of Saps1–3 antigens (MFI = 246.6) compared to BSA, with 95.5% of yeasts labeled with anti-Saps1–3 antibodies. Altogether, these results demonstrated the positive modulation of Saps' expression in C. albicans by various key host proteinaceous components, as well as by in vitro and in vivo host challenges. [ABSTRACT FROM AUTHOR]

Due to inadequate drug tissue penetration and low blood supply to the bone, the systemic delivery of medications during infection and inflammation of bone tissues frequently fails to heal abnormalities or lesions in bone tissues. In the quest for local delivery of antibiotics to treat the infection and bone-grafting particles to stimulate bone growth and regeneration, a series of composite films containing gelatin (G), chitosan (CH), carbonated hydroxyapatite (CHA), and various amounts of tetraethyl orthosilicate (TEOS) crosslinker were synthesized. The synthesis resulted in 4 (four) different composite films having a mass ratio of 0.3/0.3/0.5/x, where x = 0, 1.87, 3.73, and 5.60 for G/CH/CHA, G/CH/CHA/TEOS(2), G/CH/CHA/TEOS(4), and G/CH/CHA/TEOS(6), respectively. The composite films were characterized using SEM for morphology, SAA for specific surface area and pore volume, and FTIR and XRD for functional groups and crystal phase, respectively. Furthermore, tensile strength, water absorption capacity, polymer matrix degradation, Ca2+ release profile, drug loading capacity, drug unloading (release) profile, and drug release kinetics were determined to gain insights into the critical design parameters for preparing this drug carrier. A commercial film, Dentium™ (collagen-based), was included in the water absorption, drug loading capacity, drug release profile, and degradation tests. The biological performance of the film was evaluated from protein absorption and MC3T3I1 cell cytotoxicity. It was found that G/CH/CHA/TEOS(2) exhibited the lowest total pore volume, the highest tensile strength and protein absorption, similar water absorption and drug loading capacity, the lowest drug release rate, the lowest Ca2+ release rate, the lowest degradation rate, and cytocompatibility when compared to the other synthesized composite films. According to empirical mathematical modeling, the Higuchi and Korsmeyer-Peppas models best described the drug unloading (release) process for G/CH/CHA and G/CH/CHA/TEOS films through a diffusion process. When Dentium™ was included in the tests, Dentium™ exhibited the lowest water absorption, the lowest drug loading capacity, the highest drug release rate, and the lowest film degradation rate compared to all studied films. [ABSTRACT FROM AUTHOR]

Soybean protein isolate (SPI) is a highly functional protein source used in various food applications, such as emulsion, gelatin, and food packaging. However, its commercial application may be limited due to its poor mechanical properties, barrier properties, and high water sensitivity. Studies have shown that modifying SPI through glycosylation can enhance its functional properties and biological activities, resulting in better application performance. This paper reviews the recent studies on glycosylation modification of SPI, including its quantification method, structural improvements, and enhancement of its functional properties, such as solubility, gelation, emulsifying, and foaming. The review also discusses how glycosylation affects the bioactivity of SPI, such as its antioxidant and antibacterial activity. This review aims to provide a reference for further research on glycosylation modification and lay a foundation for applying SPI in various fields. [ABSTRACT FROM AUTHOR]

[Display omitted] Type 1 diabetes mellitus (T1DM) is a chronic disease affecting millions worldwide. Insulin therapy is currently the golden standard for treating T1DM; however, it does not restore the normal glycaemic balance entirely, which increases the risk of secondary complications. Beta-cell therapy may be a possible way of curing T1DM and has already shown promising results in the clinic. However, low retention rates, poor cell survival, and limited therapeutic potential are ongoing challenges, thus increasing the need for better cell encapsulation devices. This study aimed to develop a mechanically reinforced vascular endothelial growth factor (VEGF)-delivering encapsulation device suitable for beta cell encapsulation and transplantation. Poly(l-lactide- co -ε-caprolactone) (PLCL)/gelatin methacryloyl (GelMA)/alginate coaxial nanofibres were produced using electrospinning and embedded in an alginate hydrogel. The encapsulation device was physically and biologically characterised and was found to be suitable for INS-1E beta cell encapsulation, vascularization, and transplantation in terms of its biocompatibility, porosity, swelling ratio and mechanical properties. Lastly, VEGF was incorporated into the hydrogel and the release kinetics and functional studies revealed a sustained release of bioactive VEGF for at least 14 days, making the modified alginate system a promising candidate for improving the beta cell survival after transplantation. [ABSTRACT FROM AUTHOR]

This research uses two different dosimetry techniques (films and gels) to evaluate how γ-rays affect Cyanidin chloride. The first method relies on combining CC with poly (vinyl alcohol) to create a thin film dosimeter, while the second uses CC with gelatin to create a gel dosimeter that is more sensitive to γ-rays. The produced film or gel changes visually from red to colorless when exposed to γ-rays. The usable dose range of films was up to 35 kGy, and for gels, it was between 10 and 150 Gy. All dosimetric characteristics were studied. [ABSTRACT FROM AUTHOR]

The development of environmentally friendly, operationally simple, and easily separable adsorbents for uranium removal from wastewater holds significant importance. The biopolymer gelatin (Gel) derived from animal collagen has poor water stability, limiting its application in wastewater treatment. By in-situ compositing with ZIF-67, a nitrogen-rich and stable metal–organic framework structure introduced onto the surface of gelatin fibers enhanced the uranium adsorption capacity of gelatin nanofibers and improved the water stability of these fibers. Furthermore, through the natural polyphenolic tannic acid tanning process, it is possible to further increase selectivity of gelatin composite fibers. The gelatin composite nanofibers Gel/ZIF-67 and T-Gel/ZIF-67 were characterized using SEM, FT-IR, XRD, XPS, and contact angle. Adsorption of uranium on both nanofibers were significantly influenced by pH but minimally affected by ionic strength, indicating the inner-sphere surface complexation. The adsorption of uranium onto Gel/ZIF-67 and T-Gel/ZIF-67 followed the Langmuir isotherm model, with theoretical adsorption capacities reaching up to 608.21 mg g−1 and 612.24 mg g−1, respectively. Kinetic modeling analysis revealed that chemical adsorption played a dominant role during the adsorption processes. [ABSTRACT FROM AUTHOR]

Materials combining stretchability and sensitivity to external stimuli are key for wearable electronics applications to enable the emergence of disruptive technologies in biosensing, health monitoring, photodetection and human motion recognition. Conductive organohydrogels have gained significant attention due to their high sensitivity and cost‐effective preparation. Biopolymers like gelatin and alginate offer unique opportunities for developing responsive wearable devices, owing to their biocompatibility and sensitivity toward environmental factors. Here sustainable bio‐inspired method is presented to produce alginategelatin organohydrogels combining transparency in the visible range, ionic conductivity, high stretchability, and multiresponsiveness. The controlled alginate's crosslinking with various metal cations like Mn2+, Cu2+, Fe3+, and Zr4+ enables modulating ionic conductivity as well as finely tuning the material's thermal and mechanical properties. These organohydrogels show responsiveness to temperature (from 10 to 50 degrees, with a sensitivity of 0.19 K−1), relative humidity (from 20 to 80%, with a sensitivity of 0.022 RH(%)−1), and strain (gauge factor >1.6), enabling real‐time monitoring of environmental and physiological parameters. Remarkably, they also exhibit photoresponsivity of 9.2 µA W−1 under visible light, a feature rarely reported in literature. The ease of tuning responsiveness to the chosen stimuli and the high sensitivities open perspectives for applying these materials as wearable stretchable sensors. [ABSTRACT FROM AUTHOR]

The inherent brittleness and high cost of polylactic acid (PLA) hinder its further application. Developing low‐cost, flexible, and biodegradable gelatin (GEL)‐modified PLA is a way to broaden the application prospects of PLA applications. Acetyl tributyl citrate (ATBC) was added to overcome the process difficulty of PLA/GEL melt blending and toughening the blends. Maleic anhydride (MAH) grafted PLA (PLA‐g‐MAH) was prepared to improve the compatibility of the PLA/GEL/ATBC. Because of the interface, physical and chemical interaction induced by PLA‐g‐MAH, the compatibility among PLA, GEL, and ATBC was enhanced, which significantly improved the plasticizing efficiency of ATBC. Results showed that the elongation at break of the blends can be improved by 491%, 68 times higher than that of pristine PLA. Moreover, the modified blends did not break under the conditions of notch impact, which exhibited excellent toughness. The blends possessed a high degradation rate owing to the hydrophilic gelatin and PLA‐g‐MAH, significantly accelerated the degradation process of PLA. The prepared PLA/GEL/ATBC/PLA‐g‐MAH biomass blended plastics exhibited good comprehensive performance, with true sustainability and environmental friendliness. [ABSTRACT FROM AUTHOR]

Copyright of Modern Food Science & Technology is the property of Editorial Office of Modern Food Science & Technology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Goat skin is a potential raw material source for gelatin production using acid-ultrasound pretreatment. The objective of this study was to investigate the use of ultrasound in combination with acid pretreatment for the preparation of goat skin gelatin. Gelatin was extracted from goat skin using different pretreatments: acetic acid (T1), acetic acid followed by ultrasound (20 kHz and 750 W) (T2), and without pretreatment (T0). The results showed that the combination of acetic acid and ultrasound pretreatment significantly impacted the quality of the resulting gelatin. The study results showed an increase in yield (9.24 to 25.48%), hydroxyproline content (102.07 to 231.31 mg/g), gel strength (4.76 to 197.62 g), viscosity (6.80 to 48.00 cP), melting point (32.47 to 35.85 °C), EAI (18.24 to 23.58 m³/g), and ESI (24.90 to 62.63 min). However, there was a decrease in pH, the value of color L*, and turbidity. The SDS-PAGE patterns showed differences in molecular weight distribution due to variations in pretreatment. All gelatin samples exhibited α1 and #945;2 chains as the predominant components. Interestingly, the ultrasound effect highlighted the β-chain more boldly compared to other pretreatments. FTIR spectroscopy analysis showed changes in molecular interactions due to acetic acid pretreatment followed by ultrasound, which resulted in shifts in the Amide A, Amide B, Amide I, Amide II, and Amide III groups. Ultrasonic treatment caused more dense and disturbed structures in the sample. Therefore, the combination of acetic acid and ultrasound pretreatment yielded the superior properties of goat skin gelatin. [ABSTRACT FROM AUTHOR]

In this study, Mn3O4 nanoparticle was synthesized using Mn(CH3COO)2 and bloom gelatin as template of weight ratio 1:1 for the application in aqueous rechargeable zinc ion battery (ARZIB). The preparation of Mn3O4 was confirmed by FTIR, Raman spectra, FESEM, EDX, and XRD. Solid-state UV-Vis spectroscopic technique was used to identify its low optical band gap (2.75 eV) which indicated its semiconductor property. With additives, prepared Mn3O4 was used as cathode material, thereby CR-2032 coin cell of ARZIB was fabricated. The coin cell delivered a high specific discharge capacity of 219.33 mAh/g at 100 mA/g current density with columbic efficiency of 98.09%. It also showed excellent capacity retention, 92.69% and 64.84% after 200 and 1000 charge-discharge cycles, respectively. To check the effect of gelatin, Mn3O4 nanoparticles were further synthesized keeping the raw material constant and changing the amount of gelatin from zero to three fold. XRD was used to characterize the further prepared Mn3O4 and similar CR-2032 coin cells were fabricated and tested by cyclic voltammetry and battery charging-discharging profile. Results showed gelatin plays significant role in the surface morphology of Mn3O4 nanoparticle as well as the zinc ion storage capacity. The work offers a facile and cost-effective approach for preparing cathode material of ARZIBs. [ABSTRACT FROM AUTHOR]

This study evaluated possible utilization of infrared drying (ID) as an alternative to spray- (SD) and freeze-drying (FD) for fish skin-derived gelatins. Physical, functional, thermal, and spectroscopic analyses were conducted for characterization of the resulting gelatin powders. Energy consumption for the applied drying methods were 3.41, 8.46 and 25.33 kWh/kg for ID, SD and FD respectively, indicating that ID had the lowest energy consumption among the studied methods. Gel strength, on the other hand, was lower (398.4 g) in infrared-dried gelatin (ID-FG) compared to that (454.9 g) of freeze-dried gelatin (FD-FG) and that (472.7 g) of spray-dried gelatin (SD-FG). TGA curves indicated that ID-FG showed more resilience to thermal degradation. SDS-PAGE and UV-Vis spectra indicated that slight degradation was observed in the β-configuration of ID-FG. ID-FG and SD-FG gelatins had the highest water holding capacity (WHC), protein solubility and transparency values compared to that of FD-FG. Morphological structures of the samples were quite different as shown by SEM visuals. Ultimately, the findings showed that infrared drying may be a promising alternative for gelatin processing, maintaining product quality and supporting sustainable practices in food and other industries. [ABSTRACT FROM AUTHOR]

There is great interest in developing effective therapies for the treatment of skin wounds accompanied by deep tissue losses and severe infections. We have attempted to prepare biohybrids formed of agglomerates of mesenchymal stem cells (MSCs) with gelatin hydrogel beads (GEL beads) delivering bacteriophages (phages) as antibacterial agents and/or basic fibroblast growth factor (bFGF) for faster and better healing, providing combined therapies for these types of skin wounds. The gelatin beads were produced through a two-step process using basic and/or acidic gelatins with different isoelectric points. Escherichia coli (E. coli) and its specific T4 phages were propagated. Phages and/or bFGF were loaded within the GELs and their release rates and modes were obtained. The phage release from the basic GEL beads was quite fast; in contrast, the bFGF release from the acidic GEL beads was sustained, as anticipated. MSCs were isolated from mouse adipose tissues and 2D-cultured. Agglomerates of these MSCs with GEL beads were formed and maturated in 3D cultures, and their time-dependent changes were followed. In these 3D culture experiments, it was observed that the agglomerates with GEL beads were very healthy and the MSCs formed tissue-like structures in 7 days, while the MSC agglomerates were not healthy and shrunk considerably as a result of cell death. [ABSTRACT FROM AUTHOR]

Hydrogel materials based on sodium alginate find versatile applications in regenerative medicine and tissue engineering due to their unique properties, such as biocompatibility and biodegradability, and the possibility of the customization of their mechanical properties, such as in terms of the individual requirements of separate clinical applications. These materials, however, have numerous limitations in the area of biological activity. In order to eliminate their limitations, sodium alginate is popularly applied in combination with added gelatin, which represents a product of collagen hydrolysis. Despite numerous beneficial biological properties, matrix materials based on gelatin have poor mechanical properties and are characterized by their ability for rapid degradation in an aqueous environment, particularly at the physiological temperature of the body, which significantly limits the independent application opportunities of this type of composition in the range of scaffolding production dedicated for tissue engineering. Collagen hydrogels, unlike gelatin, are characterized by higher bioactivity, dictated by a greater number of ligands that allow for cell adhesion, as well as better stability under physiological conditions. Fish-derived collagen provides a material that may be efficiently extracted without the risk of mammalian prion infection and can be used in all patients without religious restrictions. Considering the numerous advantages of collagen indicating its superiority over gelatin, within the framework of this study, the compositions of hydrogel materials based on sodium alginate and fish collagen in different concentrations were developed. Prepared hydrogel materials were compared with the properties of a typical composition of alginate with the addition of gelatin. The rheological, mechanical, and physicochemical properties of the developed polymer compositions were evaluated. The first trials of 3D printing by extrusion technique using the analyzed polymer solutions were also conducted. The results obtained indicate that replacing gelatin with fish collagen at an analogous concentration leads to obtaining materials with a lower swelling degree, better mechanical properties, higher stability, limited release kinetics of calcium ions cross-linking the alginate matrix, a slowed process of protein release under physiological conditions, and the possibility of extrusion 3D printing. The conducted analysis highlights that the optimization of the applied concentrations of fish collagen additives to composition based on sodium alginate creates the possibility of designing materials with appropriate mechanical and rheological properties and degradation kinetics adjusted to the requirements of specific applications, leading to the prospective opportunity to produce materials capable of mimicking the properties of relevant soft tissues. Thanks to its excellent bioactivity and lower-than-gelatin viscosity of the polymer solution, fish collagen also provides a prospective solution for applications in the field of 3D bioprinting. [ABSTRACT FROM AUTHOR]

Hydrogels have the ability to retain large amounts of water within their three-dimensional polymer matrices. These attractive materials are used in medicine and the food industry; they can serve as the basis for structured food products, additives, and various ingredients. Gelatin is one of widely used biopolymers to create hydrogels that exhibit biocompatibility and tunable rheological properties. In this study, we offer a comparative analysis of rheological properties of gelatin-based hydrogels (C = 6.67%), including mammalian gelatins from bovine and porcine skins and fish gelatins from commercial samples and samples extracted from Atlantic cod skin. Mammalian gelatins provide high strength and elasticity to hydrogels. Their melting point lies in the range from 22 to 34 °C. Fish gelatin from cod skin also provides a high strength to hydrogels. Commercial fish gelatin forms weak gels exhibiting low viscoelastic properties and strength, as well as low thermal stability with a melting point of 7 °C. Gelatins were characterized basing on the analysis of amino acid composition, molecular weight distribution, and biopolymer secondary structure in gels. Our research provides a unique rheological comparison of mammalian and fish gelatin hydrogels as a tool for the re-evaluation of fish skin gelatin produced through circular processes. [ABSTRACT FROM AUTHOR]

The 3D nanopatterned silica shells of diatoms have gained attention as drug delivery vehicles because of their high porosity, extensive surface area, and compatibility with living organisms. Tooth extraction may result in various complications, including impaired blood clotting, desiccation of the root canal, and infection. Therapeutic sponges that possess multiple properties, such as the ability to stop bleeding and kill bacteria, provide numerous advantages for the healing of the area where a tooth has been removed. This study involved the fabrication of a composite material with antibacterial and hemostatic properties for dental extraction sponges. We achieved this by utilizing the porous nature and hemostatic capabilities of diatom biosilica. The antibiotic used was doxycycline. The gelatin-based diatom biosilica composite with antibiotics had the ability to prevent bleeding and release the antibiotic over a longer time compared to gelatin sponge. These properties indicate its potential as a highly promising medical device for facilitating rapid healing following tooth extraction. [ABSTRACT FROM AUTHOR]

This study investigated the effects of ultrasound treatment or calcium chloride (CaCl2) addition on the physical properties of jelly formulations. Elastic modulus (G'), loss modulus (G"), tan δ, shear modulus, yield stress (τ0), phase angle (δ), and gel strength were the parameters selected to describe the requirements of jelly printing, such as fidelity, shape retention, and extrudability. Ultrasound treatment of the jelly formulation without pectin increased the G' and shear moduli values, while decreasing the δ and gel strength. The addition of CaCl2 to the jelly formulation with pectin increased the G', G", shear modulus, τ0, and gel strength but lowered the tan δ and δ values. Both ultrasound treatment and CaCl2 addition improved the jelly printing requirements and demonstrated the potential to control the physical properties of jelly formulations for 3D printing using fused deposition modeling. [ABSTRACT FROM AUTHOR]

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Alginate–gelatin coacervation has been studied by considering different experimental parameters, such as gelatin preheating, pH, alginate–gelatin ratio and their respective concentrations, and salt effect. Results were assessed in terms of size and polydispersion via dynamic light scattering, electrostatic charge in the surface by zeta potential measurements, electrostatic interaction forces by static light scattering, stability by turbidimetry and viscoelastic and pseudoplastic behavior by rheology (oscillatory and statistical analysis). According to the results, gelatin structure has to be previously modified to induce the proper interactions with a subsequent pH reduction. Specifically, stable coacervates (according to turbidimetry and dynamic light scattering) with a size of 300–600 nm and a polydispersion lower than 0.25 were obtained after preheating the gelatin at 37°C and with a subsequent pH reduction until 4–5 for an alginate–gelatin ratio between 1:4 and 1:6. However, different experimental conditions promote an unsuccessful coacervation, obtaining always precipitates and/or coacervates with a wider particle size distribution. Furthermore, in order to study the effect of the temperature on the coacervates, different cooling–heating cycles were applied on them over a week, showing the stability of the thermo‐reversible coacervates for almost 5 days. Also, the interactions were characterized via static light scattering, analyzing the second virial coefficient. Moreover, rheological oscillatory results can be used to identify a proper coacervation due to the increase of the storage modulus. However, no significant changes were observed with statistical analysis due to the highly diluted character of the precursor solutions. These results highlighted how a proper combination of different experimental conditions, mainly temperature to promote a partial gelatin unraveling as well as pH reduction, is required to successfully produce coacervates. Finally, salt effect was proven to induce precipitation when NaCl was increasingly added to solutions of stable coacervates. [ABSTRACT FROM AUTHOR]

In this study, benzoin oleogum resin (BOGR) loaded antioxidant gelatin/pectin (GEPE) based films were developed and characterized for various parameters including mechanical, barrier, optical, film hydrophilicity/hydrophobicity, surface roughness, chemical, thermal, morphological and antioxidant properties. The incorporation of BOGR decreased water solubility, moisture content, tensile strength, and elongation at break. However, water permeability, opacity, thickness, and water hydrophobicity were increased. Moreover, SEM and AFM analysis confirmed that the films loaded with BOGR showed heterogeneous and rougher surfaces in comparison to blank film. The intermolecular interactions between GEPE and BOGR was confirmed by infrared spectroscopy. Thermal stability of the prepared BOGR loaded films was improved. Additionally, antioxidant activities of the film were significantly increased with increase in concentration of BOGR as indicated by ABTS and DPPH assays. Our findings indicate that BOGR loaded composite films could be used as an active material for food packaging applications. [ABSTRACT FROM AUTHOR]

High mortality rate of melanoma is due to the metastasis of malignant cells. Galbanic acid (GBA) is a natural sesquiterpene coumarin with valuable pharmaceutical activities. Our study aimed to investigate whether GBA can affect the migration, invasion, and adhesion of melanoma cells. The survival rate of B16F10 cells was measured using the alamarBlue assay. Scratch, adhesion, and invasion assays were performed to determine the effect of GBA on metastatic behavior of cells. Moreover, gelatin zymography was done to assess the activity of MMP-2 and MMP-9, and qRT-PCR was used to investigate the effect of GBA on the expression of candidate genes. Based on the results of alamarBlue assay, 40 µM GBA was chosen as the optimum concentration for all tests. Our findings indicated that GBA significantly decreased the invasion and migration of B16F10 cells while enhancing their adhesion ability. In addition, gelatin zymography demonstrated that GBA reduced the enzymatic activity of MMP-2 and MMP-9. Moreover, qRT-PCR revealed that GBA reduced the expression of N-cadherin and fibronectin. Current findings demonstrated, for the first time, that GBA inhibited the migration and invasion of melanoma cells via reducing the activity of MMP-2 and MMP-9 and downregulating N-cadherin and fibronectin expression. Accordingly, GBA could be suggested as a potential therapeutic agent for the treatment of melanoma. [ABSTRACT FROM AUTHOR]

Fish gelatine offers promising benefits for the nutritional and pharmaceutical industries owing to its biocompatibility, functionality, and cost-effectiveness. In the present work, the gelatine was extracted from sole fish (Solea solea) skin, and converted into nanoparticles (GeNPs), and utilised as mediators, stabilisers, and carriers for selenium nanoparticles (SeNPs). The structural characteristics of the nanoparticles and nanocomposites were characterised by using Fourier transform infrared spectroscopy (FTIR), electron microscopy, and light scattering. These analyses revealed that SeNPs were effectively and directly synthesised with the aid of GeNPs and ascorbic acid. The GeNPs exhibited spherical and smooth surfaces with a mean diameter of 281.6 nm. Conversely, the SeNPs and their composites displayed particle sizes of 35.7 and 342.8, respectively. FTIR analysis validated the structural groups and molecular interactions. The physical characterisation of fish gelatine extracted from sole fish revealed bloom gel strength of 339 g, viscosity of 14.6 cP, and a melting point of 21.2°C. Additionally, measurements of the proximate composition, colour, and gel clarity indicated that the fish gelatine exhibited favourable characteristics. The nano-gummies prepared using the nanocomposite of Ge-Selenium (NGe/Se) exhibited 72% antioxidant activity. Furthermore, the nano-gummy maintained its appearance and texture with no significant alteration after 45 days of storage. The production of NGe/Se from sole fish and the subsequent manufacturing of nano-gummies resulted in high-nutritional products with enhanced antioxidant properties and superior sensorial qualities. [ABSTRACT FROM AUTHOR]

This study investigates the development and characterization of chitosan, gelatin, and chitosan/gelatin (Chi/Gel) bioaerogel composites through a facile and eco‐friendly approach. The goal is to optimize their structural and functional properties for potential environmental and biomedical applications. Direct freezing and lyophilization approach were used to prepare the aerogels, the focus was on investigating the effects of blending ratios on the density, porosity, surface area, and water absorption capabilities of the aerogels. The results show that Chi/Gel 60/40 composition achieved an optimal balance of structural robustness and functional performance, characterized by a moderate density of 74.2 mg/cm3, the highest porosity among the samples at 93.5%, an impressive surface area of 184.8 m2/g, and a water absorption capacity of 28.8 g/g. These results suggest that the synergistic effect of chitosan and gelatin at specific ratios significantly enhances the overall properties of the material. Our findings suggest that Chi/Gel bioaerogels, especially the 60/40 composite, hold great promise for diverse applications. Highlights: All Gelatin/Chitosan bioaerogels exhibited high porosity and low density.The Chi/Gel 60/40 mix achieved the highest porosity and surface area.Highest water adsorption was observed in the Chi/Gel 60/40 composite.Synergistic effects enhanced properties of the Gelatin/Chitosan scaffolds. [ABSTRACT FROM AUTHOR]

BACKGROUNDS: Pesticides have been widely applied to promote plant growth due to their high insecticidal efficiency. However, most pesticides easily slip from the leaf surface due to the low foliar adhesion, leading to significant damage to the environment and human health. Increasing foliar adhesion of pesticides has been a major challenge. Nanomaterial technology, which can deliver pesticide active ingredients, offers a new opportunity to increase pesticides efficacy with higher foliar adhesion. RESULTS: In this study, we prepared the pesticide loaded nanohydrogel ALP@Ge‐g‐P(AA‐co‐AM)/ATP by grafting attapulgite and gelatin onto P(AA‐co‐AM), and loading the pesticide alphacypermethrin synchronously via the emulsion solvent evaporation method. The size of the new nanohydrogel was 20.5 nm and the pesticide loading capacity was 21.5%. Compared to P(AA‐co‐AM), the water absorbency of Ge‐g‐P(AA‐co‐AM)/ATP increased by 54.3% in 120 min, while the water retention increased from 4.27% to 38.7% after 48 h. Washout experiments and contact angle results suggested that the nanohydrogel, with a contact angle of 44.8° indicating good wettability, can resist rain flush and increase foliar adhesion naturally. CONCLUSIONS: Overall, the preparation of pesticide loaded nanohydrogel is simple. Experiments demonstrated the pesticide loaded nanohydrogel has high efficiency and strong foliar adhesion. This makes it a promising candidate for spraying application and reducing pollution levels. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Hydrogel 3D printing holds immense potential in fields like personalized medicine, regenerative therapies, and organ creation, offering biocompatible structures similar to the extracellular matrix. Gelatin‐Methacryloyl (GelMA) emerges as a promising candidate, while its high viscosity poses a significant challenge, especially in vat photopolymerization‐based 3D printing. Here, a new approach is presented by using Hofmeister ionic effect to substantially reduce the viscosity of high‐content (up to 60%) Gelatin bioink at room temperature with enhanced mechanical performance of the printed structures. The thinning effect induced by chaotropic Hofmeister ions is investigated through complex viscosity analysis, optical rotation measurements, and sol–gel conversion studies. The thinning effect induced by chaotropic ions enables precise 3D printing of Gelatin hydrogel, achieving accuracy comparable to prints made with polymers. Furthermore, after polymerization, the cations of the chaotropic salt change their role to cross‐linkers, leading to stronger scaffolds that exhibit biocompatibility with robust cell attachment, proliferation, and suitability for cell growth. The combination facilitates the creation of customizable structures and high printing accuracy will promote the wide application of Gelatin in the development of patient‐specific implants, drug delivery systems, and tissue scaffolds, further improving medical treatment efficacy and personalized healthcare. [ABSTRACT FROM AUTHOR]

Background: Measuring collagenase activity is crucial in the field of joint health and disease management. Collagenases, enzymes responsible for collagen degradation, play a vital role in maintaining the balance between collagen synthesis and breakdown in joints. Dysregulation of collagenase activity leads to joint tissue degradation and diseases such as rheumatoid arthritis and osteoarthritis. The development of methods to measure collagenase activity is essential for diagnosis, disease severity assessment, treatment monitoring, and identification of therapeutic targets. Results: This study aimed to validate a rapid collagenase activity detection technique using synovial fluid samples. Antibody microarray analysis was initially performed to quantify the levels of matrix metalloproteinase-9 (MMP-9), a major collagenase in joints. Subsequently, the developed gelatin-based test utilizing fluorescence measurement was used to determine collagenase activity. There was a significant correlation between the presence of MMP-9 and collagenase activity. In addition, Lower Limit of Detection and Upper Limit of Detection can be preliminary estimated as 8 ng/mL and 48 ng/mL respectively. Conclusions: The developed technique offers a potential point-of-care assessment of collagenase activity, providing real-time information for clinicians and researchers. By accurately quantifying collagenase activity, healthcare professionals can optimize patient care, improve treatment outcomes, and contribute to the understanding and management of joint-related disorders. Further research and validation are necessary to establish the full potential of this rapid collagenase activity detection method in clinical practice. [ABSTRACT FROM AUTHOR]

Background: The aim of this study was to evaluate colloids and crystalloids used in perioperative fluid therapy for cardiac surgery patients to further investigate the optimal management strategies of different solutions. Method: RCTs about adult surgical patients allocated to receive perioperative fluid therapy for electronic databases, including Ovid MEDLINE, EMBase, and Cochrane Central Register of Controlled Trials, were searched up to February 15, 2023. Results: None of the results based on network comparisons, including mortality, transfuse PLA, postoperative chest tube output over the first 24 h following surgery, and length of hospital stay, were statistically significant. Due to the small number of included studies, the results, including acute kidney injury, serum creatinine, serum microglobulin, and blood urea nitrogen, are from the direct comparison. For transfusion of RBCs, significant differences were observed in the comparisons of 3% gelatine vs. 6% HES 200/0.5, 4% albumin vs. 5% albumin, 4% gelatine vs. 5% albumin, 5% albumin vs. 6% HES 200/0.5, and 6% HES 130/0.4 vs. 6% HES 200/0.5. In transfusion of FFP, significant differences were observed in comparisons of 3% gelatine vs. 4% gelatine, 3% gelatine vs. 6% HES 200/0.5, 5% albumin vs. 6% HES 200/0.5, 4% gelatine vs. 5% albumin, 4% gelatine vs. 6% HES 200/0.4, and 6% HES 130/0.4 vs. 6% HES 200/0.5. For urinary output at 24 h after surgery, the results are deposited in the main text. Conclusion: This study showed that 3% gelatin and 5% albumin can reduce the transfuse RBC and FFP. In addition, the use of hypertonic saline solution can increase urine output, and 5% albumin and 6% HES can shorten the length of ICU stay. However, none of the perioperative fluids showed an objective advantage in various outcomes, including mortality, transfuse PLA, postoperative chest tube output over the first 24 h following surgery, and length of hospital stay. The reliable and sufficient evidences on the injury of the kidney, including acute kidney injury, serum creatinine, serum microglobulin, and blood urea nitrogen, was still lacking. In general, perioperative fluids had advantages and disadvantages, and there were no evidences to support the recommendation of the optimal perioperative fluid for cardiac surgery. [ABSTRACT FROM AUTHOR]

Skin injuries are common problems and large skin defects or infected skin needs extra attention that make the researchers find new solutions. Herein, a novel biocompatible, biodegradable antibacterial scaffold containing gelatin, TiO2, polycaprolactone, and silk fibroin loaded with different ratios of curcumin (0.5, 1, and 1.5% wt.) was fabricated with electrospinning technique and was tested with various in vitro tests. The cellular investigations (cell adhesion, cell viability, and in vitro migration test) and antibacterial assay revealed the higher efficiency of the scaffold with 1% wt. curcumin and further investigation were performed on this scaffold. The morphological observation confirmed the nanofibrous structure of the scaffold, with 0.10 ± 0.015 μm average fiber diameter. This scaffold showed hydrophilic nature with high swelling ratio absorption and 76.45 ± 5.19% degradation ratio after 2 weeks. Also, it could provide adequate mechanical properties for skin regeneration. The drug-releasing investigation revealed Cur's controlled release over 48 h. Therefore, this biocompatible and antibacterial scaffold showed high potential for treating skin injuries and is suggested for future in vivo studies. [ABSTRACT FROM AUTHOR]

Thermoresponsive hydrogels were 3D-printed with embedded gold nanorods (GNRs), which enable shape change through photothermal heating. GNRs were functionalized with bovine serum albumin and mixed with a photosensitizer and poly(N-isopropylacrylamide) (PNIPAAm) macromer, forming an ink for 3D printing by direct ink writing. A macromer-based approach was chosen to provide good microstructural homogeneity and optical transparency of the unloaded hydrogel in its swollen state. The ink was printed into an acetylated gelatin hydrogel support matrix to prevent the spreading of the low-viscosity ink and provide mechanical stability during printing and concurrent photocrosslinking. Acetylated gelatin hydrogel was introduced because it allows for melting and removal of the support structure below the transition temperature of the crosslinked PNIPAAm structure. Convective and photothermal heating were compared, which both triggered the phase transition of PNIPAAm and induced reversible shrinkage of the hydrogel–GNR composite for a range of GNR loadings. During reswelling after photothermal heating, some structures formed an internally buckled state, where minor mechanical agitation recovered the unbuckled structure. The BSA-GNRs did not leach out of the structure during multiple cycles of shrinkage and reswelling. This work demonstrates the promise of 3D-printed, photoresponsive structures as hydrogel actuators. [ABSTRACT FROM AUTHOR]

Capsules have been investigated as a popular oral dosage form among communities due to their simplicity and ease of production. Capsules that are considered in the gastro-resistance category can be very beneficial due to enhanced drug absorption, improved stability, targeted release, etc. This study investigated the effect of enteric polymers on uncoated hard capsule fabrication and dissolution properties. The polymers used in this study included HPMCPh and Eudragit L100-55. Eight different formulations based on HPMCPh, Eudragit, and gelatin were examined to identify the ideal formulation for the product of uncoated enteric hard capsules with preferred physicochemical and gastro-resistance properties. The results reveal that the capsules containing Eudragit (F1), HPMCPh (F2), Eudragit/HPMCPh/gelatin (F3), and Eudragit/gelatin (F4) are steady within the simulated stomach environment, and drug release does not occur for 120 min. The outcomes demonstrate that, among the proposed formulas, the F4 formula is suitable both in terms of capsulation form and delayed-release properties and shows no microbial growth. The properties of the optimized sample were studied by FTIR, FESEM, tensile strength, humidity, and rheology. The results illustrated that gelatin-based hydrogels with Eudragit (F4) are potential candidates for manufacturing uncoated enteric hard capsules that inhibit drug release in a gastric pH medium and act as a pH-sensitive drug-release system. [ABSTRACT FROM AUTHOR]

Tissue engineering applications in bone defect treatment have shown promising outcomes over the past decade. In this context, taking advantage of bioactive scaffolds mimicking the intrinsic composition of bone has resulted in remarkable effects on bone regeneration. In this study, Zirconium-based metal-organic framework, known as MOF 801, was synthesized and incorporated into the gelatin matrix as an osteoconductive agent to fabricate a nanocomposite bone scaffold by freeze-drying method. Physical and chemical characteristics of MOF 801 and nanocomposite scaffolds were analyzed using FE-SEM, EDS, XRD, ICP and FTIR. Besides, the biological activity of the prepared scaffolds was evaluated by MTT, alizarin red staining, crystal violet staining, and ALP assays. Inclusion of MOF 801 NPs into the scaffolds resulted in enhancement of their compressive strength up to 15 ± 0.05 MPa. The nanocomposite samples containing MOF 801 NPs also exhibited favorable bioactive feature that was confirmed by their apatite-forming ability on their surfaces upon immersion in SBF solution. The Zr ion and fumarate release studies illustrated sustained release profiles from the gelatin matrix, leading to both antioxidant and anti-inflammatory properties. MTT assay results affirmed biocompatibility of scaffolds containing up to 5 % w/w MOF 801, besides the crystal violet assay exhibited proper cell confluency and adhesion. Eventually, Alizarin red and ALP activity assays revealed that an increment of MOF 801 could induce calcium mineralization and Alkaline Phosphatase enzyme production in MG-63 cells confirming the potential of prepared scaffolds for related bone tissue engineering applications. [ABSTRACT FROM AUTHOR]

Transient electronics with degradability or dissolvability on demand possess remarkable characteristics for wearable, bioelectronic, and implanted electronic devices. While synthetic materials have made significant progress in degradability and stretchability, they suffer from intrinsic limitations, including low degradation rates, poor mechanical compliance, and high production cost, which restrict the growth of transient electronic devices. Herein, a versatile fabrication strategy is presented for transient electronics that combine a resilient biopolymer substrate (gelatin biogels) with liquid metal (Galinstan). The circuits made from gelatin biogel‐based and liquid metal are mechanically resilient and durable, exhibiting good compliance with irregular and deformable surfaces, and thus can withstand long‐term exposure to dynamic deformation (about 60 000 cycles at a strain of 50%). More importantly, gelatin biogels are naturally derived and endowed with thermally reversible gelling, which enables on‐demand rapid dissolution and recycling of the materials. As a proof‐of‐concept, transient circuit‐based capacitive sensors, which can be degraded within 20 s, are fabricated for monitoring finger touching, morse code generation, and electrical touchpad. Such a strategy provides a guideline for designing transient electronics with a combination of biopolymer gels and liquid metal, and this approach is anticipated to find applications in human–machine interfaces and wearable devices. [ABSTRACT FROM AUTHOR]